Principle of Assay
Zearalenone ELISA Test Kit (A327263) employs the competitive enzyme immunoassay technique for the quantitative measurement of Zearalenone in cereals, feed, milk, seed and oils. The 96-well microtiter plate has been pre-coated with Zearalenone. During the incubation, Zearalenone present in the samples or standards competes with the fixed amount of immobilized Zearalenone for binding sites of the Anti-Zearalenone Antibody, a HRP-Conjugated Secondary Antibody is added to the wells at the same time. The more Zearalenone present in a sample or standard, the less Anti-Zearalenone Antibody that binds to the plate. Following incubation, unbound HRP-Conjugated Secondary Antibody is removed by washing. 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 Zearalenone present in each sample or standard. The concentration of Zearalenone can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
