Principe du test
Sheep Cortisol ELISA Kit (A327162) employs the competitive enzyme immunoassay technique for the quantitative measurement of sheep Cortisol in serum and plasma. The 96-well microtiter plate has been pre-coated with Cortisol antigen. During the incubation, Cortisol present in the samples or standards competes with the fixed amount of immobilized Cortisol for binding sites on the Biotinylated Anti-Cortisol Antibody. The more Cortisol present in a sample or standard, the less Biotinylated Anti-Cortisol Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Cortisol Antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is inversely proportional to the amount of Cortisol present in each sample or standard. The concentration of Cortisol can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
