Principle of Assay
Human Neurokinin A ELISA Kit (A78523) employs the competitive enzyme immunoassay technique for the quantitative measurement of human Neurokinin A in serum, plasma, tissue homogenates, and other biological fluids. The 96-well microtiter plate has been pre-coated with Neurokinin A antigen. During the incubation, Neurokinin A present in the samples or standards competes with the fixed amount of immobilized Neurokinin A for binding sites on the Biotinylated Anti-Neurokinin A Antibody. The more Neurokinin A present in a sample or standard, the less Biotinylated Anti-Neurokinin A Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Neurokinin A 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 Neurokinin A present in each sample or standard. The concentration of Neurokinin A can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
