The Mouse Platelet-Derived Growth Factor-BB （PDGF-BB） BioAssay ELISA Kit is a quantitative sandwich assay for the detection of PDGF-BB in mouse serum，plasma，tissue homogenates and other biological fluids.Detection Range：39.063-2500pg/mlSensitivity：<23.438pg/mlAssay Principle：The microtiter plate provided in this kit has been pre-coated with an antibody specific to PDGF-BB. Standards and samples are added to the appropriate microtiter plate wells followed by a biotin-conjugated antibody specific to PDGF-BB. 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 PDGF-BB，Biotin-conjugated antibody and enzyme-conjugated Streptavidin 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 PDGF-BB in the sample is then determined by comparing the O.D. of the sample to the standard curve.Kit Components：*357966A： Microtiter Strips，8x12 wells.*357966B： Standard，2 vials357966C： Sample/Standard Dilution Buffer，1x20ml357966D： Antibody-Biotin （Concentrated），1x120ul357966E： Antibody Dilution Buffer，1x10ml357966F： Streptavidin-HRP Conjugate （SABC），1x120ul357966G： SABC Dilution Buffer，1x10ml357966H： TMB Substrate，1x10ml357966J： Stop Solution，1x10ml357966K： Wash Buffer （25X），1x30mlStorage and Stability：Store unopened *357966A at 4ºC; store at -20ºC once opened. Store unopened *357966B 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 Summary：1. Wash plate 2 times before adding standards，samples and control （zero） to wells!2. Add 100ul standard or sample to each well and incubate for 90 minutes at 37°C3. Add 100ul Antibody-Biotin working solution to each well and incubate for 60 minutes at 37°C4. 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.
