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ELISA Kit for Dopamine Beta Hydroxylase (DbH) - SEB429Hu

ELISA Kit for Dopamine Beta Hydroxylase (DbH) - SEB429Hu

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ELISA Kit for Dopamine Beta Hydroxylase (DbH) Sizes: 24T, 48T, 96T Catalogue Numbers: SEB429Hu-24, SEB429Hu-48, SEB429Hu-96 Citations, Manuals and MSDS Available upon request. Featured Series: Sandwich kit Target: Dopamine Beta Hydroxylase Alternative Names: DBM; Dopamine Beta-Monooxygenase Target Species: Human Uniprot: P09172 Gene ID: 1621 Featured Series Function: Detects protein (regular version) Specificity: Reactive with Human DbH / Dopamine Beta Hydroxylase Method: Colormetric Detection principle: Double-antibody Sandwich Detection range: 3.12-200ng/mL Sensitivity: 1.22ng/mL Assay Time: 3h Sample Size: 100uL Recommended/Predicted Sample Types: Serum, Plasma, Tissue Homogenates and other Biological Fluids Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12% Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life) Shelf-life: 12 months Specificity: This assay has high sensitivity and excellent specificity for detection of Dopamine Beta Hydroxylase (DbH). No significant cross-reactivity or interference between Dopamine Beta Hydroxylase (DbH) and analogues was observed. Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Dopamine Beta Hydroxylase (DbH) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Dopamine Beta Hydroxylase (DbH) 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. Target: 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. Test 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 Dopamine Beta Hydroxylase (DbH). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Dopamine Beta Hydroxylase (DbH). 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 Dopamine Beta Hydroxylase (DbH), 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 Dopamine Beta Hydroxylase (DbH) in the samples is then determined by comparing the O.D. of the samples to the standard curve. Research Area: Neuro science; Research Use Only