Principle of Assay
Bovine Aldosterone ELISA Kit (A87433) employs the competitive enzyme immunoassay technique for the quantitative measurement of bovine Aldosterone in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with Aldosterone antigen. During the incubation, Aldosterone present in the samples or standards competes with the fixed amount of immobilized Aldosterone for binding sites on the Biotinylated Anti-Aldosterone Antibody. The more Aldosterone present in a sample or standard, the less Biotinylated Anti-Aldosterone Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Aldosterone 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 Aldosterone present in each sample or standard. The concentration of Aldosterone can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
