0.312-20ng/ml

<0.188ng/ml

Intra-Assay CV: <8% Inter-Assay CV: <10%

*370058A: Microtiter Strips, 1x96 wells (8x12 wells). *370058B: Standard, 2x1 vial 370058C: Sample/Standard Dilution Buffer, 1x20ml 370058D: Antibody (Biotin) (Concentrated), 1x120ul 370058E: Antibody Dilution Buffer, 1x10ml 370058F: Streptavidin (HRP) (SABC), 1x120ul 370058G: SABC Dilution Buffer, 1x10ml 370058H: TMB Substrate, 1x10ml 370058J: Stop Solution, 1x10ml 370058K: Wash Buffer, 25X, 1x30ml

Store unopened *370058A at 4ºC; store at -20ºC once opened. Store unopened *370058B at 4°C; once reconstituted, store at 4°C for up to 12 hours or at -20°C for up to 48 hours. Store other components at 4°C. Kit is stable for 6 months after receipt. For maximum recovery of product, centrifuge the original vials after thawing and prior to removing the cap.

This ELISA kit employs the sandwich enzyme-linked immunoassay technique, utilizing a microtiter plate pre-coated with an antibody specific to IRS1. Standards and samples are added to the appropriate wells, then incubated. Aspirate and wash the plate. The Antibody (Biotin) is added to all the wells. The plate is incubated and then washed. Streptavidin (HRP) is added to each microplate well and incubated then washed. Then the TMB substrate solution is added and incubated. After the TMB substrate solution is added, only those wells that contain IRS1, the Antibody (Biotin) and Streptavidin (HRP) will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulfuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of IRS1 in the sample is then determined by comparing the O.D. of the sample to the standard curve.

1. Wash plate 2 times before adding standards and samples to wells! 2. Add 100ul standard or sample to each well and incubate for 90 minutes at 37°C. Aspirate and wash 2 times. 3. Add 100ul Antibody (Biotin) working solution to each well and incubate for 60 minutes at 37°C. 4. Aspirate and wash 3 times. 5. Add 100ul SABC working solution to each well. Incubate for 30 minutes at 37°C 6. Aspirate and wash 5 times. 7. Add 90ul TMB substrate. Incubate 15-30 minutes at 37°C 8. Add 50ul Stop Solution. Read at 450nm immediately. 9. Calculate results.