{"title":"USCN","description":"","products":[{"product_id":"elisa-kit-for-calprotectin-calpro-usek504ca","title":"ELISA Kit for Calprotectin (CALPRO) - USEK504Ca","description":"\u003cp\u003eELISA Kit for Calprotectin (CALPRO)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: USEK504Ca-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Calprotectin (CALPRO)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: MRP-8\/MRP-14; S100A8\/A9\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Dog\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 0.78-50ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.30ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: C0LQL0\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 490461\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (regular version)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 3h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Dog CALPRO \/ Calprotectin\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Double-antibody Sandwich\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 100uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Calprotectin (CALPRO).\u003cbr\u003e\nNo significant cross-reactivity or interference between Calprotectin (CALPRO) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Calprotectin (CALPRO) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Calprotectin (CALPRO) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 3 times;\u003cbr\u003e\n5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n6. Aspirate and wash 5 times;\u003cbr\u003e\n7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n8. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microplate provided in this kit has been pre-coated with an antibody specific to S100A8. Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to S100A9. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain calprotectin, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of calprotectin in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065238195,"sku":"USEK504Ca-96","price":400.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-creatine-kinase-mb-isoenzyme-ckmb-usea479hu","title":"ELISA Kit for Creatine Kinase MB Isoenzyme (CKMB) - USEA479Hu","description":"\u003cp\u003eELISA Kit for Creatine Kinase MB Isoenzyme (CKMB)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: USEA479Hu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Creatine Kinase MB Isoenzyme (CKMB)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: CK2; CK-MB; Creatine Kinase,Muscle\/Brain\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 1.56-100ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.59ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P06732 \u0026amp; P12277\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 1158 \u0026amp; 1152\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (regular version)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 3h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Human CKMB \/ Creatine Kinase MB Isoenzyme\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Double-antibody Sandwich\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 100uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Creatine Kinase MB Isoenzyme (CKMB).\u003cbr\u003e\nNo significant cross-reactivity or interference between Creatine Kinase MB Isoenzyme (CKMB) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Creatine Kinase MB Isoenzyme (CKMB) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Creatine Kinase MB Isoenzyme (CKMB) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 3 times;\u003cbr\u003e\n5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n6. Aspirate and wash 5 times;\u003cbr\u003e\n7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n8. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microplate provided in this kit has been pre-coated with an antibody specific to CKMM. Standardsor samplesare then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific toCKBB. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain CKMB, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of CKMB in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Enzyme \u0026amp; Kinase; Cardiovascular biology;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065270963,"sku":"USEA479Hu-96","price":315.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-chemokine-c-c-motif-receptor-3-ccr3-usea910hu","title":"ELISA Kit for Chemokine C-C-Motif Receptor 3 (CCR3) - USEA910Hu","description":"\u003cp\u003eELISA Kit for Chemokine C-C-Motif Receptor 3 (CCR3)\u003c\/p\u003e\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\u003cp\u003eCatalogue Number: USEA910Hu-96\u003c\/p\u003e\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\u003cp\u003eTarget: Chemokine C-C-Motif Receptor 3 (CCR3) \u003c\/p\u003e\n\u003cp\u003eAlternative Names: CD193; CC-CKR3; C-C CKR-3; CMKBR3; CKR3; Eosinophil eotaxin receptor\u003c\/p\u003e\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\u003cp\u003eDetection range: 31.2-2,000pg\/mL\u003c\/p\u003e\n\u003cp\u003eSensitivity: 11.7pg\/mL Uniprot: P51677 \u003c\/p\u003e\n\u003cp\u003eGene ID: 1232\u003c\/p\u003e\n\u003cp\u003eFeatured Series Function: Detects protein (regular version)\u003c\/p\u003e\n\u003cp\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003c\/p\u003e\n\u003cp\u003eAssay Time: 3h Method: Colormetric\u003c\/p\u003e\n\u003cp\u003eSpecificity: Reactive with Human CCR3 \/ Chemokine C-C-Motif Receptor 3 \u003c\/p\u003e\n\u003cp\u003eDetection principle: Double-antibody Sandwich\u003c\/p\u003e\n\u003cp\u003eSample Size: 100uL\u003c\/p\u003e\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\u003cp\u003eShelf-life: 12 months Specificity: This assay has high sensitivity and excellent specificity for detection of Chemokine C-C-Motif Receptor 3 (CCR3). No significant cross-reactivity or interference between Chemokine C-C-Motif Receptor 3 (CCR3) and analogues was observed. Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Chemokine C-C-Motif Receptor 3 (CCR3) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Chemokine C-C-Motif Receptor 3 (CCR3) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD\/meanX100 Stability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards; 2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C; 3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C; 4. Aspirate and wash 3 times; 5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C; 6. Aspirate and wash 5 times; 7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C; 8. Add 50µL Stop Solution. Read at 450nm immediately. T\u003c\/p\u003e\n\u003cp\u003eest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Chemokine C-C-Motif Receptor 3 (CCR3). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Chemokine C-C-Motif Receptor 3 (CCR3). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Chemokine C-C-Motif Receptor 3 (CCR3), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Chemokine C-C-Motif Receptor 3 (CCR3) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\u003cp\u003eResearch Area: CD \u0026amp; Adhesion molecule; Tumor immunity; Infection immunity; \u003c\/p\u003e\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065303731,"sku":"USEA910Hu-96","price":315.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-programmed-cell-death-protein-4-pdcd4-usel108hu","title":"ELISA Kit for Programmed Cell Death Protein 4 (PDCD4) - USEL108Hu","description":"ELISA Kit for Programmed Cell Death Protein 4 (PDCD4)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEL108Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Programmed Cell Death Protein 4 (PDCD4)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: H731; Neoplastic Transformation Inhibitor; Nuclear antigen H731-like; Protein 197\/15a\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.055ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q53EL6\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 27250\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human PDCD4 \/ Programmed Cell Death Protein 4\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Programmed Cell Death Protein 4 (PDCD4).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Programmed Cell Death Protein 4 (PDCD4) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Programmed Cell Death Protein 4 (PDCD4) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Programmed Cell Death Protein 4 (PDCD4) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Programmed Cell Death Protein 4 (PDCD4). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Programmed Cell Death Protein 4 (PDCD4). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Programmed Cell Death Protein 4 (PDCD4), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Programmed Cell Death Protein 4 (PDCD4) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Tumor immunity; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065336499,"sku":"USEL108Hu-96","price":385.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"mini-samples-elisa-kit-for-interleukin-4-il4-umea077hu","title":"Mini Samples ELISA Kit for Interleukin 4 (IL4) - UMEA077Hu","description":"Mini Samples ELISA Kit for Interleukin 4 (IL4)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: UMEA077Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Interleukin 4 (IL4)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: BSF1; BCGF1 ; B Cell Stimulatory Factor 1; Lymphocyte stimulatory factor 1; B Cell Growth Factor; Binetrakin; Pitrakinra\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 15.6-1,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 6.2pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P05112\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 3565\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (micro-volume samples 15-25 μl)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human IL4 \/ Interleukin 4\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 15-25uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Mini Samples Interleukin 4 (IL4).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Mini Samples Interleukin 4 (IL4) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Interleukin 4 (IL4) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Interleukin 4 (IL4) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 25µL standard or sample to each well. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 25µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 25µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 25µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 20µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mini Samples Interleukin 4 (IL4). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Mini Samples Interleukin 4 (IL4). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mini Samples Interleukin 4 (IL4), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mini Samples Interleukin 4 (IL4) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Cytokine; Immune molecule; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065369267,"sku":"UMEA077Hu-96","price":299.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-interleukin-23-il23-usex262mu","title":"ELISA Kit for Interleukin 23 (IL23) - USEX262Mu","description":"ELISA Kit for Interleukin 23 (IL23)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEX262Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Interleukin 23 (IL23)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 15.6-1,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 5.6pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P43432 \u0026amp; Q9EQ14\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 16160 \u0026amp; 83430\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse IL23 \/ Interleukin 23\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Interleukin 23 (IL23).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Interleukin 23 (IL23) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Interleukin 23 (IL23) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Interleukin 23 (IL23) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Interleukin 23 (IL23). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Interleukin 23 (IL23). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Interleukin 23 (IL23), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Interleukin 23 (IL23) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065434803,"sku":"USEX262Mu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-z-dna-binding-protein-1-zbp1-useb552hu","title":"ELISA Kit for Z-DNA Binding Protein 1 (ZBP1) - USEB552Hu","description":"ELISA Kit for Z-DNA Binding Protein 1 (ZBP1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEB552Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Z-DNA Binding Protein 1 (ZBP1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: DLM1; DAI; DNA-Dependent Activator Of IRFs; Tumor stroma and activated macrophage protein DLM-1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.059ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q9H171\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 81030\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human ZBP1 \/ Z-DNA Binding Protein 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Z-DNA Binding Protein 1 (ZBP1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Z-DNA Binding Protein 1 (ZBP1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Z-DNA Binding Protein 1 (ZBP1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Z-DNA Binding Protein 1 (ZBP1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Z-DNA Binding Protein 1 (ZBP1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Z-DNA Binding Protein 1 (ZBP1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Z-DNA Binding Protein 1 (ZBP1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Z-DNA Binding Protein 1 (ZBP1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; Developmental science; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065467571,"sku":"USEB552Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-cystathionine-beta-synthase-cbs-usej484mu","title":"ELISA Kit for Cystathionine Beta Synthase (CbS) - USEJ484Mu","description":"ELISA Kit for Cystathionine Beta Synthase (CbS)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEJ484Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Cystathionine Beta Synthase (CbS)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: HIP4; Beta-thionase; Serine sulfhydrase\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.312-20ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.122ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q91WT9\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 12411\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse CbS \/ Cystathionine Beta Synthase\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Cystathionine Beta Synthase (CbS).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Cystathionine Beta Synthase (CbS) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Cystathionine Beta Synthase (CbS) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Cystathionine Beta Synthase (CbS) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Cystathionine Beta Synthase (CbS). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Cystathionine Beta Synthase (CbS). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Cystathionine Beta Synthase (CbS), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Cystathionine Beta Synthase (CbS) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Enzyme \u0026amp; Kinase; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065500339,"sku":"USEJ484Mu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-stem-cell-factor-scf-usea120po","title":"ELISA Kit for Stem Cell Factor (SCF) - USEA120Po","description":"ELISA Kit for Stem Cell Factor (SCF)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEA120Po-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Stem Cell Factor (SCF)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: KITLG; MGF; SF; KL1; Kitl; FPH2; Kit-Ligand; Steel Factor; Mast Cell Growth Factor; Steel factor; Familial Progressive Hyperpigmentation 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Pig\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 15.6-1,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 6.0pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q29030\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 397509\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Pig SCF \/ Stem Cell Factor\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Stem Cell Factor (SCF).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Stem Cell Factor (SCF) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Stem Cell Factor (SCF) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Stem Cell Factor (SCF) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Stem Cell Factor (SCF). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Stem Cell Factor (SCF). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Stem Cell Factor (SCF), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Stem Cell Factor (SCF) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Cytokine; Hematology; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065533107,"sku":"USEA120Po-96","price":378.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-erythropoietin-epo-usea028eq","title":"ELISA Kit for Erythropoietin (EPO) - USEA028Eq","description":"ELISA Kit for Erythropoietin (EPO)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEA028Eq-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Erythropoietin (EPO)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: EP; Epoetin; Erythropoetin; Hematopoietin; Hemopoietin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Horse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 31.2-2,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 11.9pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q867B1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 100033849\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Horse EPO \/ Erythropoietin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Erythropoietin (EPO).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Erythropoietin (EPO) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Erythropoietin (EPO) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Erythropoietin (EPO) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Erythropoietin (EPO). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Erythropoietin (EPO). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Erythropoietin (EPO), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Erythropoietin (EPO) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Cytokine; Endocrinology; Hematology; Hormone metabolism; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065565875,"sku":"USEA028Eq-96","price":387.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-solute-carrier-family-7-member-11-slc7a11-usee410hu","title":"ELISA Kit for Solute Carrier Family 7, Member 11 (SLC7A11) - USEE410Hu","description":"ELISA Kit for Solute Carrier Family 7, Member 11 (SLC7A11)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEE410Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Solute Carrier Family 7, Member 11 (SLC7A11)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: CCBR1; xCT; Cystine\/Glutamate Transporter,Cationic Amino Acid Transporter,y+ System; Amino acid transport system xc-; Calcium channel blocker resistance protein CCBR1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.057ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q9UPY5\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 23657\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human SLC7A11 \/ Solute Carrier Family 7, Member 11\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Solute Carrier Family 7, Member 11 (SLC7A11).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Solute Carrier Family 7, Member 11 (SLC7A11) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Solute Carrier Family 7, Member 11 (SLC7A11) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Solute Carrier Family 7, Member 11 (SLC7A11) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Solute Carrier Family 7, Member 11 (SLC7A11). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Solute Carrier Family 7, Member 11 (SLC7A11). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Solute Carrier Family 7, Member 11 (SLC7A11), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Solute Carrier Family 7, Member 11 (SLC7A11) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065598643,"sku":"USEE410Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-fission-1-fis1-usej105ra","title":"ELISA Kit for Fission 1 (FIS1) - USEJ105Ra","description":"ELISA Kit for Fission 1 (FIS1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEJ105Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Fission 1 (FIS1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: CGI-135; TTC11; Tetratricopeptide Repeat Domain 11; Mitochondrial fission 1 protein\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.312-20ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.115ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P84817\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 288584\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat FIS1 \/ Fission 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Fission 1 (FIS1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Fission 1 (FIS1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Fission 1 (FIS1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Fission 1 (FIS1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Fission 1 (FIS1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Fission 1 (FIS1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Fission 1 (FIS1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Fission 1 (FIS1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Tumor immunity; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065631411,"sku":"USEJ105Ra-96","price":380.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-sjogren-syndrome-antigen-a2-ssa2-used197mu","title":"ELISA Kit for Sjogren Syndrome Antigen A2 (SSA2) - USED197Mu","description":"ELISA Kit for Sjogren Syndrome Antigen A2 (SSA2)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USED197Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Sjogren Syndrome Antigen A2 (SSA2)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: RO60; TROVE2; RoRNP; TROVE Domain Family,Member 2; 60kDa Ribonucleoprotein Autoantigen SS-A\/Ro; Autoantigen Ro, 60kDa; TROVE domain family member 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.062ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: O08848\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 20822\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse SSA2 \/ Sjogren Syndrome Antigen A2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Sjogren Syndrome Antigen A2 (SSA2).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Sjogren Syndrome Antigen A2 (SSA2) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Sjogren Syndrome Antigen A2 (SSA2) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Sjogren Syndrome Antigen A2 (SSA2) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Sjogren Syndrome Antigen A2 (SSA2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Sjogren Syndrome Antigen A2 (SSA2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Sjogren Syndrome Antigen A2 (SSA2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Sjogren Syndrome Antigen A2 (SSA2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Immune molecule; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065664179,"sku":"USED197Mu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-anti-podocin-antibody-anti-pdcn-uaea938hu","title":"ELISA Kit for Anti-Podocin Antibody (Anti-PDCN) - UAEA938Hu","description":"\u003cp\u003eELISA Kit for Anti-Podocin Antibody (Anti-PDCN)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UAEA938Hu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Anti-Podocin Antibody (Anti-PDCN)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: NPHS2; NPHS-2; Nephrosis 2; Idiopathic Steroid-Resistant\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 3.12-200ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 1.19ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: Q9NP85\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 7827\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (antigen)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h, 30min\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Human Anti-PDCN \/ Anti-Podocin Antibody\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Anti-Podocin Antibody (Anti-PDCN).\u003cbr\u003e\nNo significant cross-reactivity or interference between Anti-Podocin Antibody (Anti-PDCN) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Anti-Podocin Antibody (Anti-PDCN) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Anti-Podocin Antibody (Anti-PDCN) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 5 times;\u003cbr\u003e\n5. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n6. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Podocin Antibody (Anti-PDCN) will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Anti-Podocin Antibody (Anti-PDCN) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Infection immunity; Kidney biomarker;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065696947,"sku":"UAEA938Hu-96","price":378.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-anti-desmoglein-3-antibody-anti-dsg3-uaea444hu","title":"ELISA Kit for Anti-Desmoglein 3 Antibody (Anti-DSG3) - UAEA444Hu","description":"\u003cp\u003eELISA Kit for Anti-Desmoglein 3 Antibody (Anti-DSG3)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UAEA444Hu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Anti-Desmoglein 3 Antibody (Anti-DSG3)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: CDHF6; PVA; 130 kDa pemphigus vulgaris antigen; Cadherin family member 6\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 1.56-100ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.57ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P32926\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 1830\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (antigen)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h, 30min\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Human Anti-DSG3 \/ Anti-Desmoglein 3 Antibody\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Anti-Desmoglein 3 Antibody (Anti-DSG3).\u003cbr\u003e\nNo significant cross-reactivity or interference between Anti-Desmoglein 3 Antibody (Anti-DSG3) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Anti-Desmoglein 3 Antibody (Anti-DSG3) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Anti-Desmoglein 3 Antibody (Anti-DSG3) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 5 times;\u003cbr\u003e\n5. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n6. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Desmoglein 3 Antibody (Anti-DSG3) will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Anti-Desmoglein 3 Antibody (Anti-DSG3) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: CD \u0026amp; Adhesion molecule; Infection immunity;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065729715,"sku":"UAEA444Hu-96","price":425.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-anti-desmoglein-1-antibody-anti-dsg1-uaea729hu","title":"ELISA Kit for Anti-Desmoglein 1 Antibody (Anti-DSG1) - UAEA729Hu","description":"\u003cp\u003eELISA Kit for Anti-Desmoglein 1 Antibody (Anti-DSG1)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UAEA729Hu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Anti-Desmoglein 1 Antibody (Anti-DSG1)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: CDHF4; DG1; DSG; Cadherin family member 4; Desmosomal glycoprotein 1; Pemphigus foliaceus antigen\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 1.56-100ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.55ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: Q02413\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 1828\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (antigen)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h, 30min\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Human Anti-DSG1 \/ Anti-Desmoglein 1 Antibody\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Anti-Desmoglein 1 Antibody (Anti-DSG1).\u003cbr\u003e\nNo significant cross-reactivity or interference between Anti-Desmoglein 1 Antibody (Anti-DSG1) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Anti-Desmoglein 1 Antibody (Anti-DSG1) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Anti-Desmoglein 1 Antibody (Anti-DSG1) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 5 times;\u003cbr\u003e\n5. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n6. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Desmoglein 1 Antibody (Anti-DSG1) will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Anti-Desmoglein 1 Antibody (Anti-DSG1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: CD \u0026amp; Adhesion molecule; Dermatology; Autoimmunity;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065762483,"sku":"UAEA729Hu-96","price":425.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-anti-proprotein-convertase-subtilisin-kexin-type-9-antibody-anti-pcsk9-uaee189mu","title":"ELISA Kit for Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9) - UAEE189Mu","description":"\u003cp\u003eELISA Kit for Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UAEE189Mu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: FH3; HCHOLA3; NARC1; Hypercholesterolemia,Autosomal Dominant 3; Neural apoptosis-regulated convertase 1; Proprotein convertase 9; Subtilisin\/kexin-like protease PC9\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Mouse\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 1.56-100ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.57ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: Q80W65\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 100102\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (antigen)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h, 30min\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Mouse Anti-PCSK9 \/ Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9).\u003cbr\u003e\nNo significant cross-reactivity or interference between Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 5 times;\u003cbr\u003e\n5. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n6. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9) will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Anti-Proprotein Convertase Subtilisin\/Kexin Type 9 Antibody (Anti-PCSK9) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Enzyme \u0026amp; Kinase;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065795251,"sku":"UAEE189Mu-96","price":432.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-procalcitonin-pct-usea689po","title":"ELISA Kit for Procalcitonin (PCT) - USEA689Po","description":"ELISA Kit for Procalcitonin (PCT)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEA689Po-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Procalcitonin (PCT)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: Pro-Calcitonin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Pig\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 1.56-100pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.55pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P30880\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Pig PCT \/ Procalcitonin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Procalcitonin (PCT).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Procalcitonin (PCT) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Procalcitonin (PCT) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Procalcitonin (PCT) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Procalcitonin (PCT). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Procalcitonin (PCT). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Procalcitonin (PCT), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Procalcitonin (PCT) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Infection immunity; Hormone metabolism; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065828019,"sku":"USEA689Po-96","price":420.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-neuroglobin-ngb-usea606ra","title":"ELISA Kit for Neuroglobin (NGB) - USEA606Ra","description":"ELISA Kit for Neuroglobin (NGB)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEA606Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Neuroglobin (NGB)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.065ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q99JA8\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 85382\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat NGB \/ Neuroglobin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Neuroglobin (NGB).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Neuroglobin (NGB) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Neuroglobin (NGB) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Neuroglobin (NGB) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Neuroglobin (NGB). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Neuroglobin (NGB). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Neuroglobin (NGB), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Neuroglobin (NGB) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Metabolic pathway; Neuroscience; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065860787,"sku":"USEA606Ra-96","price":342.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-protein-kinase-amp-activated-beta-1-prkab1-useb671ra","title":"ELISA Kit for Protein Kinase, AMP Activated Beta 1 (PRKAb1) - USEB671Ra","description":"ELISA Kit for Protein Kinase, AMP Activated Beta 1 (PRKAb1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEB671Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Protein Kinase, AMP Activated Beta 1 (PRKAb1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: AMPK; HAMPKb; 5'-AMP-Activated Protein Kinase Subunit Beta-1 Non-Catalytic Subunit; Adenosine Monophosphate Activated Protein Kinase(AMPK)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.055ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P80386\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 83803\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat PRKAb1 \/ Protein Kinase, AMP Activated Beta 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Protein Kinase, AMP Activated Beta 1 (PRKAb1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Protein Kinase, AMP Activated Beta 1 (PRKAb1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Protein Kinase, AMP Activated Beta 1 (PRKAb1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Protein Kinase, AMP Activated Beta 1 (PRKAb1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Protein Kinase, AMP Activated Beta 1 (PRKAb1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Protein Kinase, AMP Activated Beta 1 (PRKAb1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Protein Kinase, AMP Activated Beta 1 (PRKAb1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Protein Kinase, AMP Activated Beta 1 (PRKAb1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Enzyme \u0026amp; Kinase; Metabolic pathway; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065893555,"sku":"USEB671Ra-96","price":361.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-meteorin-metrn-useh662hu","title":"ELISA Kit for Meteorin (METRN) - USEH662Hu","description":"ELISA Kit for Meteorin (METRN)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEH662Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Meteorin (METRN)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: C16orf23; RJD6; Glial Cell Differentiation Regulator\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.057ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q9UJH8\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 79006\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human METRN \/ Meteorin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Meteorin (METRN).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Meteorin (METRN) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Meteorin (METRN) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Meteorin (METRN) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Meteorin (METRN). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Meteorin (METRN). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Meteorin (METRN), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Meteorin (METRN) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Neuroscience; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065926323,"sku":"USEH662Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-carboxypeptidase-a3-cpa3-usec395ra","title":"ELISA Kit for Carboxypeptidase A3 (CPA3) - USEC395Ra","description":"ELISA Kit for Carboxypeptidase A3 (CPA3)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEC395Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Carboxypeptidase A3 (CPA3)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: MC-CPA; Mast cell carboxypeptidase A; Carboxypeptidase A3, Mast Cell\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.781-50ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.25ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P21961\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 54242\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat CPA3 \/ Carboxypeptidase A3\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Carboxypeptidase A3 (CPA3).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Carboxypeptidase A3 (CPA3) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Carboxypeptidase A3 (CPA3) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Carboxypeptidase A3 (CPA3) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Carboxypeptidase A3 (CPA3). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Carboxypeptidase A3 (CPA3). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Carboxypeptidase A3 (CPA3), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Carboxypeptidase A3 (CPA3) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Enzyme \u0026amp; Kinase; Infection immunity; Rheumatology; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065959091,"sku":"USEC395Ra-96","price":380.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-chemokine-c-c-motif-receptor-10-ccr10-useb024mu","title":"ELISA Kit for Chemokine C-C-Motif Receptor 10 (CCR10) - USEB024Mu","description":"ELISA Kit for Chemokine C-C-Motif Receptor 10 (CCR10)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEB024Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Chemokine C-C-Motif Receptor 10 (CCR10)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: GPR2; G Protein-Coupled Receptor 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.054ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q9JL21\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 12777\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse CCR10 \/ Chemokine C-C-Motif Receptor 10\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Chemokine C-C-Motif Receptor 10 (CCR10).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Chemokine C-C-Motif Receptor 10 (CCR10) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Chemokine C-C-Motif Receptor 10 (CCR10) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Chemokine C-C-Motif Receptor 10 (CCR10) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Chemokine C-C-Motif Receptor 10 (CCR10). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Chemokine C-C-Motif Receptor 10 (CCR10). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Chemokine C-C-Motif Receptor 10 (CCR10), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Chemokine C-C-Motif Receptor 10 (CCR10) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; CD \u0026amp; Adhesion molecule; Tumor immunity; Infection immunity; Dermatology; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390065991859,"sku":"USEB024Mu-96","price":342.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-extracellular-signal-regulated-kinase-2-erk2-usea930ra","title":"ELISA Kit for Extracellular Signal Regulated Kinase 2 (ERK2) - USEA930Ra","description":"ELISA Kit for Extracellular Signal Regulated Kinase 2 (ERK2)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEA930Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Extracellular Signal Regulated Kinase 2 (ERK2)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: MAPK1; P38; P40; ERK2; ERT1; MAPK2; P42MAPK; P42-MAPK; PRKM1; PRKM2; P41; P41mapk; P41-mapk; Mitogen-Activated Protein Kinase 1; Mitogen-activated protein kinase 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.060ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P63086\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 116590\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat ERK2 \/ Extracellular Signal Regulated Kinase 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Extracellular Signal Regulated Kinase 2 (ERK2).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Extracellular Signal Regulated Kinase 2 (ERK2) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Extracellular Signal Regulated Kinase 2 (ERK2) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Extracellular Signal Regulated Kinase 2 (ERK2) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Extracellular Signal Regulated Kinase 2 (ERK2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Extracellular Signal Regulated Kinase 2 (ERK2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Extracellular Signal Regulated Kinase 2 (ERK2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Extracellular Signal Regulated Kinase 2 (ERK2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; Enzyme \u0026amp; Kinase; Tumor immunity; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066024627,"sku":"USEA930Ra-96","price":342.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-scavenger-receptor-class-b-member-1-scarb1-useh194mu","title":"ELISA Kit for Scavenger Receptor Class B Member 1 (SCARB1) - USEH194Mu","description":"ELISA Kit for Scavenger Receptor Class B Member 1 (SCARB1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEH194Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Scavenger Receptor Class B Member 1 (SCARB1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: CD36L1; SRB1; CLA1, SR-BI; Collagen Type I Receptor Thrombospondin Receptor-Like 1; CD36 and LIMPII analogous 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.057ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q61009\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 20778\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse SCARB1 \/ Scavenger Receptor Class B Member 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Scavenger Receptor Class B Member 1 (SCARB1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Scavenger Receptor Class B Member 1 (SCARB1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Scavenger Receptor Class B Member 1 (SCARB1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Scavenger Receptor Class B Member 1 (SCARB1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Scavenger Receptor Class B Member 1 (SCARB1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Scavenger Receptor Class B Member 1 (SCARB1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Scavenger Receptor Class B Member 1 (SCARB1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Scavenger Receptor Class B Member 1 (SCARB1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: CD \u0026amp; Adhesion molecule; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066057395,"sku":"USEH194Mu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-interleukin-18-il18-usea064gu","title":"ELISA Kit for Interleukin 18 (IL18) - USEA064Gu","description":"ELISA Kit for Interleukin 18 (IL18)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEA064Gu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Interleukin 18 (IL18)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: IGIF; IL-1g; IL1F4; IL1-F4; Interferon-Gamma-Inducing Factor; Interleukin-1 Family Member 4; Iboctadekin; Interleukin-1 Gamma\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Guinea pig\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 15.6-1,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 5.7pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: D6RR58\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 100734451\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Guinea pig IL18 \/ Interleukin 18\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Interleukin 18 (IL18).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Interleukin 18 (IL18) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Interleukin 18 (IL18) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Interleukin 18 (IL18) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Interleukin 18 (IL18). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Interleukin 18 (IL18). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Interleukin 18 (IL18), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Interleukin 18 (IL18) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Cytokine; Infection immunity; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066090163,"sku":"USEA064Gu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-histone-cluster-1-h4a-hist1h4a-useq004hu","title":"ELISA Kit for Histone Cluster 1, H4a (HIST1H4A) - USEQ004Hu","description":"ELISA Kit for Histone Cluster 1, H4a (HIST1H4A)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEQ004Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Histone Cluster 1, H4a (HIST1H4A)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: H4FA; HIST2H4B; HIST2H4C; HIST2H4D; HIST2H4E; HIST2H4F; HIST2H4G; HIST2H4H; HIST2H4I; HIST2H4J; HIST2H4K; HIST2H4B; HIST4H4; HIST2H4A\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.057ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P62805\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 121504\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human HIST1H4A \/ Histone Cluster 1, H4a\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Histone Cluster 1, H4a (HIST1H4A).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Histone Cluster 1, H4a (HIST1H4A) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Histone Cluster 1, H4a (HIST1H4A) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Histone Cluster 1, H4a (HIST1H4A) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Histone Cluster 1, H4a (HIST1H4A). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Histone Cluster 1, H4a (HIST1H4A). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Histone Cluster 1, H4a (HIST1H4A), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Histone Cluster 1, H4a (HIST1H4A) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Metabolic pathway; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066122931,"sku":"USEQ004Hu-96","price":385.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-advillin-avil-useg172hu","title":"ELISA Kit for Advillin (AVIL) - USEG172Hu","description":"ELISA Kit for Advillin (AVIL)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEG172Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Advillin (AVIL)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: ADVIL; p92; DOC6\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.054ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: O75366\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 10677\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human AVIL \/ Advillin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Advillin (AVIL).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Advillin (AVIL) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Advillin (AVIL) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Advillin (AVIL) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Advillin (AVIL). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Advillin (AVIL). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Advillin (AVIL), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Advillin (AVIL) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066155699,"sku":"USEG172Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-insulin-receptor-substrate-1-irs1-usec546ra","title":"ELISA Kit for Insulin Receptor Substrate 1 (IRS1) - USEC546Ra","description":"ELISA Kit for Insulin Receptor Substrate 1 (IRS1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEC546Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Insulin Receptor Substrate 1 (IRS1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: HIRS1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.058ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P35570\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 25467\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat IRS1 \/ Insulin Receptor Substrate 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Insulin Receptor Substrate 1 (IRS1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Insulin Receptor Substrate 1 (IRS1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Insulin Receptor Substrate 1 (IRS1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Insulin Receptor Substrate 1 (IRS1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Insulin Receptor Substrate 1 (IRS1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Insulin Receptor Substrate 1 (IRS1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Insulin Receptor Substrate 1 (IRS1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Insulin Receptor Substrate 1 (IRS1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Endocrinology; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066188467,"sku":"USEC546Ra-96","price":380.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-brevican-bcan-usec177ra","title":"ELISA Kit for Brevican (BCAN) - USEC177Ra","description":"ELISA Kit for Brevican (BCAN)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEC177Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Brevican (BCAN)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: BEHAB; CSPG7; Chondroitin Sulfate Proteoglycan 7; Brevican Proteoglycan; Brevican core protein; Brain-enriched hyaluronan-binding protein\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 78-5,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 30pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P55068\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 25393\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat BCAN \/ Brevican\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Brevican (BCAN).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Brevican (BCAN) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Brevican (BCAN) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Brevican (BCAN) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Brevican (BCAN). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Brevican (BCAN). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Brevican (BCAN), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Brevican (BCAN) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Neuroscience; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066221235,"sku":"USEC177Ra-96","price":380.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-myosin-light-chain-3-alkali-ventricular-slow-skeletal-myl3-used425ra","title":"ELISA Kit for Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3) - USED425Ra","description":"ELISA Kit for Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USED425Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: CMH8; MLC1V; VLC1; MLC1SB; Cardiac myosin light chain 1; Ventricular\/slow twitch myosin alkali light chain\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.057ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P16409\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 24585\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat MYL3 \/ Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Myosin Light Chain 3, Alkali, Ventricular, Slow Skeletal (MYL3) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Metabolic pathway; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066254003,"sku":"USED425Ra-96","price":380.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-purinergic-receptor-p2x-ligand-gated-ion-channel-4-p2rx4-useg074hu","title":"ELISA Kit for Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4) - USEG074Hu","description":"ELISA Kit for Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEG074Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: P2X4; P2X4R; P2X Purinoceptor 4; ATP receptor; Purinergic receptor\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.312-20ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.119ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q99571\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 5025\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human P2RX4 \/ Purinergic Receptor P2X, Ligand Gated Ion Channel 4\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Purinergic Receptor P2X, Ligand Gated Ion Channel 4 (P2RX4) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: CD \u0026amp; Adhesion molecule; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066286771,"sku":"USEG074Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-platelet-factor-4-pf4-ucea172rb","title":"ELISA Kit for Platelet Factor 4 (PF4) - UCEA172Rb","description":"\u003cp\u003eELISA Kit for Platelet Factor 4 (PF4)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UCEA172Rb-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Platelet Factor 4 (PF4)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: CXCL4; SCYB4; Chemokine C-X-C-Motif Ligand 4; Oncostatin-A; Iroplact\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Rabbit\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 2.47-200ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.87ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P02776\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 5196\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects small molecule\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Platelet-Poor Plasma and Cell Culture Supernates\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Rabbit PF4 \/ Platelet Factor 4\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Platelet Factor 4 (PF4).\u003cbr\u003e\nNo significant cross-reactivity or interference between Platelet Factor 4 (PF4) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Platelet Factor 4 (PF4) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Platelet Factor 4 (PF4) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 50µL standard or sample to each well.\u003cbr\u003e\n And then add 50µL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 50µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to PF4 has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled PF4 and unlabeled PF4 (Standards or samples) with the pre-coated antibody specific to PF4. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of PF4 in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of PF4 in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Cytokine; Hematology;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066319539,"sku":"UCEA172Rb-96","price":361.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"clia-kit-for-tryptase-beta-2-tpsb2-uscd781hu","title":"CLIA Kit for Tryptase Beta 2 (TPSb2) - USCD781Hu","description":"\u003cp\u003eCLIA Kit for Tryptase Beta 2 (TPSb2)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: USCD781Hu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Tryptase Beta 2 (TPSb2)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: TPS2; Tryptase Beta II; Tryptase Beta III\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 0.55-400pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.20pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P20231\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 64499\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (regular version)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h, 40min\u003c\/p\u003e\n\n\u003cp\u003eMethod: Chemiluminescence\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Human TPSb2 \/ Tryptase Beta 2\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Double-antibody Sandwich\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 100uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Tryptase Beta 2 (TPSb2).\u003cbr\u003e\nNo significant cross-reactivity or interference between Tryptase Beta 2 (TPSb2) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Tryptase Beta 2 (TPSb2) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Tryptase Beta 2 (TPSb2) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 3 times;\u003cbr\u003e\n5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n6. Aspirate and wash 5 times;\u003cbr\u003e\n7. Add 100µL Substrate Solution. Incubate 10 minutes at 37°C;\u003cbr\u003e\n8. Read RLU value immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microplate provided in this kit has been pre-coated with an antibody specific to Tryptase Beta 2 (TPSb2). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Tryptase Beta 2 (TPSb2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Tryptase Beta 2 (TPSb2) level in the sample or standard.;\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Infection immunity;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066352307,"sku":"USCD781Hu-96","price":420.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-myosin-binding-protein-c-slow-type-mybpc1-used413hu","title":"ELISA Kit for Myosin Binding Protein C, Slow Type (MYBPC1) - USED413Hu","description":"ELISA Kit for Myosin Binding Protein C, Slow Type (MYBPC1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USED413Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Myosin Binding Protein C, Slow Type (MYBPC1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: MYBPCC; MYBPCS; C-protein, skeletal muscle slow isoform\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.058ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q00872\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 4604\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human MYBPC1 \/ Myosin Binding Protein C, Slow Type\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Myosin Binding Protein C, Slow Type (MYBPC1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Myosin Binding Protein C, Slow Type (MYBPC1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Myosin Binding Protein C, Slow Type (MYBPC1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Myosin Binding Protein C, Slow Type (MYBPC1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Myosin Binding Protein C, Slow Type (MYBPC1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Myosin Binding Protein C, Slow Type (MYBPC1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Myosin Binding Protein C, Slow Type (MYBPC1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Myosin Binding Protein C, Slow Type (MYBPC1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Metabolic pathway; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066385075,"sku":"USED413Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-carboxylesterase-3-ces3-usef283hu","title":"ELISA Kit for Carboxylesterase 3 (CES3) - USEF283Hu","description":"ELISA Kit for Carboxylesterase 3 (CES3)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEF283Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Carboxylesterase 3 (CES3)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: Br3; ES31; Brain carboxylesterase 3; Esterase 31; Liver carboxylesterase 31 homolog\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.063ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q6UWW8\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 23491\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human CES3 \/ Carboxylesterase 3\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Carboxylesterase 3 (CES3).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Carboxylesterase 3 (CES3) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Carboxylesterase 3 (CES3) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Carboxylesterase 3 (CES3) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Carboxylesterase 3 (CES3). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Carboxylesterase 3 (CES3). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Carboxylesterase 3 (CES3), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Carboxylesterase 3 (CES3) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Enzyme \u0026amp; Kinase; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066417843,"sku":"USEF283Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-creatine-cr-ucev807ge","title":"ELISA Kit for Creatine (Cr) - UCEV807Ge","description":"\u003cp\u003eELISA Kit for Creatine (Cr)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UCEV807Ge-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Creatine (Cr)\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: General species\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 1.23-100ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 0.53ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects small molecule\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with General species Cr \/ Creatine\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Creatine (Cr).\u003cbr\u003e\nNo significant cross-reactivity or interference between Creatine (Cr) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Creatine (Cr) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Creatine (Cr) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 50µL standard or sample to each well.\u003cbr\u003e\n And then add 50µL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 50µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Creatine (Cr) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Creatine (Cr) and unlabeled Creatine (Cr) (Standards or samples) with the pre-coated antibody specific to Creatine (Cr). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Creatine (Cr) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Creatine (Cr) in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390066450611,"sku":"UCEV807Ge-96","price":465.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-high-mobility-group-box-protein-2-hmgb2-usec052hu","title":"ELISA Kit for High Mobility Group Box Protein 2 (HMGB2) - USEC052Hu","description":"ELISA Kit for High Mobility Group Box Protein 2 (HMGB2)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEC052Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: High Mobility Group Box Protein 2 (HMGB2)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: HMG2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.312-20ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.115ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P26583\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 3148\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human HMGB2 \/ High Mobility Group Box Protein 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of High Mobility Group Box Protein 2 (HMGB2).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between High Mobility Group Box Protein 2 (HMGB2) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level High Mobility Group Box Protein 2 (HMGB2) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level High Mobility Group Box Protein 2 (HMGB2) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to High Mobility Group Box Protein 2 (HMGB2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to High Mobility Group Box Protein 2 (HMGB2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain High Mobility Group Box Protein 2 (HMGB2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of High Mobility Group Box Protein 2 (HMGB2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; Tumor immunity; Developmental science; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068547763,"sku":"USEC052Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-anti-apolipoprotein-b-antibody-anti-apob-uaec003hu","title":"ELISA Kit for Anti-Apolipoprotein B Antibody (Anti-APOB) - UAEC003Hu","description":"\u003cp\u003eELISA Kit for Anti-Apolipoprotein B Antibody (Anti-APOB)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UAEC003Hu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Anti-Apolipoprotein B Antibody (Anti-APOB)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: Apo-B; FLDB; Apo B-100\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Human\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 3.12-200ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 1.22ng\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P04114\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 338\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (antigen)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h, 30min\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Human Anti-APOB \/ Anti-Apolipoprotein B Antibody\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Anti-Apolipoprotein B Antibody (Anti-APOB).\u003cbr\u003e\nNo significant cross-reactivity or interference between Anti-Apolipoprotein B Antibody (Anti-APOB) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Anti-Apolipoprotein B Antibody (Anti-APOB) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Anti-Apolipoprotein B Antibody (Anti-APOB) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cbr\u003e\n3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cbr\u003e\n4. Aspirate and wash 5 times;\u003cbr\u003e\n5. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n6. Add 50µL Stop Solution. Read at 450nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Apolipoprotein B Antibody (Anti-APOB) will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Anti-Apolipoprotein B Antibody (Anti-APOB) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Metabolic pathway; Endocrinology; Cardiovascular biology; Hepatology; Nutrition metabolism;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068580531,"sku":"UAEC003Hu-96","price":400.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-glyoxalase-i-glo1-usec501mu","title":"ELISA Kit for Glyoxalase I (GLO1) - USEC501Mu","description":"ELISA Kit for Glyoxalase I (GLO1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEC501Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Glyoxalase I (GLO1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: GLY-I; GLOD1; Glyoxalase Domain Containing 1; Lactoylglutathione lyase; Aldoketomutase; Ketone-aldehyde mutase; Methylglyoxalase; S-D-lactoylglutathione methylglyoxal lyase\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 78-5,000pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 32pg\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q9CPU0\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 109801\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse GLO1 \/ Glyoxalase I\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Glyoxalase I (GLO1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Glyoxalase I (GLO1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Glyoxalase I (GLO1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Glyoxalase I (GLO1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Glyoxalase I (GLO1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Glyoxalase I (GLO1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Glyoxalase I (GLO1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Glyoxalase I (GLO1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Enzyme \u0026amp; Kinase; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068613299,"sku":"USEC501Mu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-methylmalonyl-coenzyme-a-mutase-mut-used691hu","title":"ELISA Kit for Methylmalonyl Coenzyme A Mutase (MUT) - USED691Hu","description":"ELISA Kit for Methylmalonyl Coenzyme A Mutase (MUT)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USED691Hu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Methylmalonyl Coenzyme A Mutase (MUT)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: MCM; Methylmalonyl-CoA isomerase; Methylmalonyl-CoA mutase, mitochondrial\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Human\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.156-10ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.059ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P22033\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 4594\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Human MUT \/ Methylmalonyl Coenzyme A Mutase\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Methylmalonyl Coenzyme A Mutase (MUT).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Methylmalonyl Coenzyme A Mutase (MUT) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Methylmalonyl Coenzyme A Mutase (MUT) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Methylmalonyl Coenzyme A Mutase (MUT) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Methylmalonyl Coenzyme A Mutase (MUT). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Methylmalonyl Coenzyme A Mutase (MUT). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Methylmalonyl Coenzyme A Mutase (MUT), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Methylmalonyl Coenzyme A Mutase (MUT) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Enzyme \u0026amp; Kinase; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068646067,"sku":"USED691Hu-96","price":350.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-transcription-elongation-factor-a1-tcea1-used971mu","title":"ELISA Kit for Transcription Elongation Factor A1 (TCEA1) - USED971Mu","description":"ELISA Kit for Transcription Elongation Factor A1 (TCEA1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USED971Mu-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Transcription Elongation Factor A1 (TCEA1)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: GTF2S; SII; TCEA; TF2S; TFIIS; Transcription elongation factor S-II protein 1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Mouse\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.312-20ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.119ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P10711\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 21399\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Mouse TCEA1 \/ Transcription Elongation Factor A1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Transcription Elongation Factor A1 (TCEA1).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Transcription Elongation Factor A1 (TCEA1) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Transcription Elongation Factor A1 (TCEA1) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Transcription Elongation Factor A1 (TCEA1) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Transcription Elongation Factor A1 (TCEA1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Transcription Elongation Factor A1 (TCEA1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Transcription Elongation Factor A1 (TCEA1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Transcription Elongation Factor A1 (TCEA1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Reproductive science; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068678835,"sku":"USED971Mu-96","price":360.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"mini-samples-elisa-kit-for-amylin-umea812ra","title":"Mini Samples ELISA Kit for Amylin - UMEA812Ra","description":"\u003cp\u003eMini Samples ELISA Kit for Amylin\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UMEA812Ra-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Amylin (Amylin)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: IAPP; IAP; DAP; Islet Amyloid Polypeptide; Insulinoma Amyloid Polypeptide; Diabetes-associated peptide\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Rat\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 12.35-1,000pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 4.37pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P12969\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 24476\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (micro-volume samples 15-25 μl)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 3h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Rat Amylin \/ Amylin\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 15-25uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Mini Samples Amylin.\u003cbr\u003e\nNo significant cross-reactivity or interference between Mini Samples Amylin and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Amylin were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Amylin were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 25µL standard or sample to each well.\u003cbr\u003e\n And then add 25μL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 50µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 50µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 25µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Mini Samples Amylin has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Mini Samples Amylin and unlabeled Mini Samples Amylin (Standards or samples) with the pre-coated antibody specific to Mini Samples Amylin. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Mini Samples Amylin in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Mini Samples Amylin in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Metabolic pathway; Endocrinology; Hepatology;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068711603,"sku":"UMEA812Ra-96","price":411.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"mini-samples-elisa-kit-for-pancreatic-polypeptide-pp-umeb265ra","title":"Mini Samples ELISA Kit for Pancreatic Polypeptide (PP) - UMEB265Ra","description":"\u003cp\u003eMini Samples ELISA Kit for Pancreatic Polypeptide (PP)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UMEB265Ra-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Pancreatic Polypeptide (PP)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: PPY; PNP; Pancreatic Polypeptide Y; Obinepitide; Pancreatic icosapeptide; Pancreatic prohormone\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Rat\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 24.69-2,000pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 9.04pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P06303\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 24677\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (micro-volume samples 15-25 μl)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 3h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Rat PP \/ Pancreatic Polypeptide\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 15-25uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Mini Samples Pancreatic Polypeptide (PP).\u003cbr\u003e\nNo significant cross-reactivity or interference between Mini Samples Pancreatic Polypeptide (PP) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Pancreatic Polypeptide (PP) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Pancreatic Polypeptide (PP) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 25µL standard or sample to each well.\u003cbr\u003e\n And then add 25μL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 50µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 50µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 25µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Mini Samples Pancreatic Polypeptide (PP) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Mini Samples Pancreatic Polypeptide (PP) and unlabeled Mini Samples Pancreatic Polypeptide (PP) (Standards or samples) with the pre-coated antibody specific to Mini Samples Pancreatic Polypeptide (PP). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Mini Samples Pancreatic Polypeptide (PP) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Mini Samples Pancreatic Polypeptide (PP) in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Endocrinology;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068744371,"sku":"UMEB265Ra-96","price":463.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"mini-samples-elisa-kit-for-ghrelin-ghrl-umea991ra","title":"Mini Samples ELISA Kit for Ghrelin (GHRL) - UMEA991Ra","description":"\u003cp\u003eMini Samples ELISA Kit for Ghrelin (GHRL)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UMEA991Ra-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Ghrelin (GHRL)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: MTLRP; Growth Hormone-Releasing Peptide\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Rat\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 123.5-10,000pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 51.5pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: Q9QYH7\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 59301\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (micro-volume samples 15-25 μl)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 3h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Rat GHRL \/ Ghrelin\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 15-25uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Mini Samples Ghrelin (GHRL).\u003cbr\u003e\nNo significant cross-reactivity or interference between Mini Samples Ghrelin (GHRL) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Ghrelin (GHRL) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Ghrelin (GHRL) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 25µL standard or sample to each well.\u003cbr\u003e\n And then add 25μL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 50µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 50µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 25µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Mini Samples Ghrelin (GHRL) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Mini Samples Ghrelin (GHRL) and unlabeled Mini Samples Ghrelin (GHRL) (Standards or samples) with the pre-coated antibody specific to Mini Samples Ghrelin (GHRL). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Mini Samples Ghrelin (GHRL) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Mini Samples Ghrelin (GHRL) in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Signal transduction; Metabolic pathway; Endocrinology; Gastroenterology; Hormone metabolism;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068777139,"sku":"UMEA991Ra-96","price":411.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"mini-samples-elisa-kit-for-c-peptide-cp-umea447ra","title":"Mini Samples ELISA Kit for C-Peptide (CP) - UMEA447Ra","description":"\u003cp\u003eMini Samples ELISA Kit for C-Peptide (CP)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UMEA447Ra-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: C-Peptide (CP)\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Rat\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 123.5-10,000pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 47.4pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P01322\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 24505\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects protein (micro-volume samples 15-25 μl)\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 3h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Rat CP \/ C-Peptide\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 15-25uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Mini Samples C-Peptide (CP).\u003cbr\u003e\nNo significant cross-reactivity or interference between Mini Samples C-Peptide (CP) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples C-Peptide (CP) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples C-Peptide (CP) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 25µL standard or sample to each well.\u003cbr\u003e\n And then add 25μL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 50µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 50µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 25µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Mini Samples C-Peptide (CP) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Mini Samples C-Peptide (CP) and unlabeled Mini Samples C-Peptide (CP) (Standards or samples) with the pre-coated antibody specific to Mini Samples C-Peptide (CP). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Mini Samples C-Peptide (CP) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Mini Samples C-Peptide (CP) in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Endocrinology; Hormone metabolism;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068809907,"sku":"UMEA447Ra-96","price":365.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-transcription-factor-a-mitochondrial-tfam-useh050ra","title":"ELISA Kit for Transcription Factor A, Mitochondrial (TFAM) - USEH050Ra","description":"ELISA Kit for Transcription Factor A, Mitochondrial (TFAM)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: USEH050Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Transcription Factor A, Mitochondrial (TFAM)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: MtTF1; TCF6; TCF6L2; mtTFA; Mitochondrial transcription factor 1; Transcription factor 6-like 2\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 0.312-20ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 0.112ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: Q91ZW1\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 83474\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (regular version)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Tissue Homogenates, Cell Lysates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat TFAM \/ Transcription Factor A, Mitochondrial\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 100uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Transcription Factor A, Mitochondrial (TFAM).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Transcription Factor A, Mitochondrial (TFAM) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Transcription Factor A, Mitochondrial (TFAM) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Transcription Factor A, Mitochondrial (TFAM) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 100µL standard or sample to each well. Incubate 1 hours at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 50µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Transcription Factor A, Mitochondrial (TFAM). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Transcription Factor A, Mitochondrial (TFAM). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Transcription Factor A, Mitochondrial (TFAM), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Transcription Factor A, Mitochondrial (TFAM) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Signal transduction; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068842675,"sku":"USEH050Ra-96","price":380.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"mini-samples-elisa-kit-for-osteonectin-on-umea791ra","title":"Mini Samples ELISA Kit for Osteonectin (ON) - UMEA791Ra","description":"Mini Samples ELISA Kit for Osteonectin (ON)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSize: 96T\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCatalogue Number: UMEA791Ra-96\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eCitations, Manuals and MSDS Available upon request.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget: Osteonectin (ON)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAlternative Names: SPARC; BM-40; Secreted Protein,Acidic,Cysteine-Rich; Basement-membrane protein 40; Secreted protein acidic and rich in cysteine\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTarget Species: Rat\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection range: 6.25-400ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSensitivity: 2.79ng\/mL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eUniprot: P16975\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eGene ID: 24791\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eFeatured Series Function: Detects protein (micro-volume samples 15-25 μl)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Time: 3h\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eMethod: Colormetric\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: Reactive with Rat ON \/ Osteonectin\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eDetection principle: Double-antibody Sandwich\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSample Size: 15-25uL\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eShelf-life: 12 months\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Mini Samples Osteonectin (ON).\u003cp\u003e\u003c\/p\u003eNo significant cross-reactivity or interference between Mini Samples Osteonectin (ON) and analogues was observed.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mini Samples Osteonectin (ON) were tested 20 times on one plate, respectively.\u003cp\u003e\u003c\/p\u003eInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mini Samples Osteonectin (ON) were tested on 3 different plates, 8 replicates in each plate.\u003cp\u003e\u003c\/p\u003eCV(%) = SD\/meanX100\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cp\u003e\u003c\/p\u003eTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cp\u003e\u003c\/p\u003e2. Add 25µL standard or sample to each well. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e3. Aspirate and add 25µL prepared Detection Reagent A. Incubate 1 hour at 37°C;\u003cp\u003e\u003c\/p\u003e4. Aspirate and wash 3 times;\u003cp\u003e\u003c\/p\u003e5. Add 25µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e6. Aspirate and wash 5 times;\u003cp\u003e\u003c\/p\u003e7. Add 25µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cp\u003e\u003c\/p\u003e8. Add 20µL Stop Solution. Read at 450nm immediately.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eTest principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Mini Samples Osteonectin (ON). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Mini Samples Osteonectin (ON). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Mini Samples Osteonectin (ON), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Mini Samples Osteonectin (ON) in the samples is then determined by comparing the O.D. of the samples to the standard curve.\u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Area: Metabolic pathway; Tumor immunity; Infection immunity; Hepatology; Bone metabolism; \u003cp\u003e\u003c\/p\u003e\u003cp\u003e\u003c\/p\u003eResearch Use Only","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068875443,"sku":"UMEA791Ra-96","price":411.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-orexin-a-oxa-ucea607mu","title":"ELISA Kit for Orexin A (OXA) - UCEA607Mu","description":"\u003cp\u003eELISA Kit for Orexin A (OXA)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UCEA607Mu-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Orexin A (OXA)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: Hypocretin-1\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Mouse\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 12.35-1,000pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 5.05pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: O55241\u003c\/p\u003e\n\n\u003cp\u003eGene ID: 15171\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects small molecule\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Mouse OXA \/ Orexin A\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Orexin A (OXA).\u003cbr\u003e\nNo significant cross-reactivity or interference between Orexin A (OXA) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Orexin A (OXA) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Orexin A (OXA) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 50µL standard or sample to each well.\u003cbr\u003e\n And then add 50µL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 50µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Orexin A (OXA) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Orexin A (OXA) and unlabeled Orexin A (OXA) (Standards or samples) with the pre-coated antibody specific to Orexin A (OXA). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Orexin A (OXA) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Orexin A (OXA) in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Neuroscience; Gastroenterology; Hormone metabolism;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068908211,"sku":"UCEA607Mu-96","price":342.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"},{"product_id":"elisa-kit-for-neurofilament-light-polypeptide-nefl-ucee038po","title":"ELISA Kit for Neurofilament, Light Polypeptide (NEFL) - UCEE038Po","description":"\u003cp\u003eELISA Kit for Neurofilament, Light Polypeptide (NEFL)\u003c\/p\u003e\n\n\u003cp\u003eSize: 96T\u003c\/p\u003e\n\n\u003cp\u003eCatalogue Number: UCEE038Po-96\u003c\/p\u003e\n\n\u003cp\u003eCitations, Manuals and MSDS Available upon request.\u003c\/p\u003e\n\n\u003cp\u003eTarget: Neurofilament, Light Polypeptide (NEFL)\u003c\/p\u003e\n\n\u003cp\u003eAlternative Names: CMT1F; CMT2E; NF-L; NF68; NFL; 68 kDa neurofilament protein; Neurofilament triplet L protein\u003c\/p\u003e\n\n\u003cp\u003eTarget Species: Pig\u003c\/p\u003e\n\n\u003cp\u003eDetection range: 123.5-10,000pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eSensitivity: 50.3pg\/mL\u003c\/p\u003e\n\n\u003cp\u003eUniprot: P02547\u003c\/p\u003e\n\n\u003cp\u003eFeatured Series Function: Detects small molecule\u003c\/p\u003e\n\n\u003cp\u003eRecommended\/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids\u003c\/p\u003e\n\n\u003cp\u003eAssay Time: 2h\u003c\/p\u003e\n\n\u003cp\u003eMethod: Colormetric\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: Reactive with Pig NEFL \/ Neurofilament, Light Polypeptide\u003c\/p\u003e\n\n\u003cp\u003eDetection principle: Competitive Inhibition\u003c\/p\u003e\n\n\u003cp\u003eSample Size: 50uL\u003c\/p\u003e\n\n\u003cp\u003eAssay Precision: Intra-Assay: CV\u0026lt;10%, Inter-Assay: CV\u0026lt;12%\u003c\/p\u003e\n\n\u003cp\u003eStorage: 4°C for 1 month\/ -20°C for long-term(One year within shelf life)\u003c\/p\u003e\n\n\u003cp\u003eShelf-life: 12 months\u003c\/p\u003e\n\n\u003cp\u003eSpecificity: This assay has high sensitivity and excellent specificity for detection of Neurofilament, Light Polypeptide (NEFL).\u003cbr\u003e\nNo significant cross-reactivity or interference between Neurofilament, Light Polypeptide (NEFL) and analogues was observed.\u003c\/p\u003e\n\n\u003cp\u003ePrecision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Neurofilament, Light Polypeptide (NEFL) were tested 20 times on one plate, respectively.\u003cbr\u003e\nInter-assay Precision (Precision between assays): 3 samples with low, middle and high level Neurofilament, Light Polypeptide (NEFL) were tested on 3 different plates, 8 replicates in each plate.\u003cbr\u003e\nCV(%) = SD\/meanX100\u003c\/p\u003e\n\n\u003cp\u003eStability: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.\u003cbr\u003e\nTo minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.\u003c\/p\u003e\n\n\u003cp\u003eAssay procedure summary: 1. Prepare all reagents, samples and standards;\u003cbr\u003e\n2. Add 50µL standard or sample to each well.\u003cbr\u003e\n And then add 50µL prepared Detection Reagent A immediately.\u003cbr\u003e\n Shake and mix. Incubate 1 hour at 37°C;\u003cbr\u003e\n3. Aspirate and wash 3 times;\u003cbr\u003e\n4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;\u003cbr\u003e\n5. Aspirate and wash 5 times;\u003cbr\u003e\n6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;\u003cbr\u003e\n7. Add 50µL Stop Solution. Read at 450 nm immediately.\u003c\/p\u003e\n\n\u003cp\u003eTest principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Neurofilament, Light Polypeptide (NEFL) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Neurofilament, Light Polypeptide (NEFL) and unlabeled Neurofilament, Light Polypeptide (NEFL) (Standards or samples) with the pre-coated antibody specific to Neurofilament, Light Polypeptide (NEFL). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Neurofilament, Light Polypeptide (NEFL) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Neurofilament, Light Polypeptide (NEFL) in the sample.\u003c\/p\u003e\n\n\u003cp\u003eResearch Area: Neuroscience;\u003c\/p\u003e \n\n\u003cp\u003eResearch Use Only\u003c\/p\u003e","brand":"USCN","offers":[{"title":"Default Title","offer_id":45390068940979,"sku":"UCEE038Po-96","price":399.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/files\/USCN.png?v=1774797733"}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0305\/9482\/6376\/collections\/LOGO_Clipped_for_website_dbcbf3df-9525-4ae9-bd11-1ca6c83f5175.png?v=1774449470","url":"https:\/\/afsbio.com\/collections\/uscn.oembed?page=15","provider":"AFSBio Inc.","version":"1.0","type":"link"}