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GCSF ADA (granulocyte colony stimulating factor) ELISA - EL-141-73196

GCSF ADA (granulocyte colony stimulating factor) ELISA - EL-141-73196

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GCSF ADA (granulocyte colony stimulating factor) ELISA

Catalogue Number: EL-141-73196

Size: 1X96 wells

Antigen: antibodies to GCSF

Storage: -20°C, 1 year

Reactivity: Human

Detection Range: 45 ng/mL -1440 ng/mL

Detection Minimum: 45 ng/mL

Protocol: This assay employs the indirect enzyme immunoassay technique. GCSF is coated onto a 96 well microplate. Calibrator and test samples are prepared by dilution into assay buffer and are pipetted into the appropriate wells. Antibodies to GCSF present in biological matrices are bound to the immobilized GCSF. After washing away any unbound substances, antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of antibodies to GCSF present in the calibrator and test samples. The color development is stopped and the intensity of the color is measured.

Components: Coated microtiter plate, 96 wells (12x8 strips) 1 Calibrator diluent 1.8 ml Calibrator (1.15mg/mL) 12 μl 10X wash buffer 50 ml Assay buffer 50 ml 1000X detection reagent 17 μl TMB 12 ml TMB stop solution

Method Type: Direct sandwich ELISA

Detection Method: Peroxidase / OD450

Principle: Quantification of antibodies to G-CSF

Plate: Strip

Sample Type: Serum Plasma

Sample Volume: 15ul

Assay Time: 2.5 hours

Specificity: anti-GCSF antibodies

Assay Precision: <20%, <20%

Preservative: none

Description: Granulocyte colony-stimulating factor (G-CSF or GCSF), also known as colony-stimulating factor 3 (CSF 3), is a glycoprotein that stimulates the bone marrow to produce granulocytes and stem cells and release them into the bloodstream

Gene ID: N/ap

Assay Procedure: This assay employs the indirect enzyme immunoassay technique. GCSF is coated onto a 96 well microplate. Calibrator and test samples are prepared by dilution into assay buffer and are pipetted into the appropriate wells. Antibodies to GCSF present in biological matrices are bound to the immobilized GCSF. After washing away any unbound substances, antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of antibodies to GCSF present in the calibrator and test samples. The color development is stopped and the intensity of the color is measured

Reagent Preparation: Prepare only the appropriate amount of required
reagent on the day of use. Store all reagents as per
instructions stated on the label.1. Wash Buffer (1X) Preparation:Dilute wash buffer concentrate with ultra-pure water 1/20 before use (for example, add 50mL wash buffer concentrate to 450mL ultra-pure water). Mix well. 2. Detection Reagent (1X) Preparation: Dilute detection reagent with assay buffer 1/1000 before use (for example add 11μl concentrate to 11ml of assay buffer). Mix well. 3. Calibrator Preparation: Dilute the calibrator from 1.15mg/ml down to 11.5µg/ml by pipetting 5µl of calibrator stock into 495µl assay buffer. Label "Cal. Int." Mix well. Prepare calibrators with concentrations ranging from 1440ng/ml to 45ng/ml. The following is an example calibrator curve

Results Calculation: 1. Construct a standard curve by plotting the absorbance obtained from each standard against concentration. Use a 4 or 5 parameter curve fit. 2. The concentration of the unknowns can be back calculated directly from this standard curve using the absorbance value for each sample.

Sample Collection: This kit is compatible with EDTA-plasma, heparinplasma and serum samples. Samples can be stored at or below -20°C for up to 1 year.

Sample Preparation: Dilute calibrators and test samples 1/50 with assay buffer (for example add 5µl of prepared calibrator or sample to 245µl of assay buffer). Mix well. Do not store diluted samples.