Growth Hormone （GH） BioAssay ELISA Kit is a quantitative sandwich assay for the detection of GH in sheep serum，plasma，tissue homogenates and other biological fluids.Detection Range：0.156-10ng/mlSensitivity：<0.094ng/mlPrecision： Intra-Assay CV： <8%Inter-Assay CV： <10%Kit Components：*369932A： Microtiter Strips，1x96 wells （8x12 wells）.*369932B： Standard，2x1 vial369932C： Sample/Standard Dilution Buffer，1x20ml369932D： Antibody （Biotin） （Concentrated），1x120ul369932E： Antibody Dilution Buffer，1x10ml369932F： Streptavidin （HRP） （SABC），1x120ul369932G： SABC Dilution Buffer，1x10ml369932H： TMB Substrate，1x10ml369932J： Stop Solution，1x10ml369932K： Wash Buffer，25X，1x30mlStorage and Stability：Store unopened *369932A at 4ºC; store at -20ºC once opened. Store unopened *369932B 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.Assay Principle：The microtiter plate provided in this kit has been pre-coated with an antibody specific to GH. Standards and samples are added to the appropriate microtiter plate wells followed by a biotin-conjugated antibody specific to GH. Streptavidin conjugated to Horseradish Peroxidase （HRP） is added to each microplate well and incubated. After TMB substrate solution is added，only those wells that contain GH，Biotin-conjugated antibody and enzyme-conjugated Streptavidin complex 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 GH in the sample is then determined by comparing the O.D. of the sample to the standard curve.Assay Summary：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°C6. Aspirate and wash 5 times.7. Add 90ul TMB substrate. Incubate 15-30 minutes at 37°C8. Add 50ul Stop Solution. Read at 450nm immediately.9. Calculate results.
