Principle of Assay
Human Luteinizing Hormone beta ELISA Kit (A330031) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human Luteinizing Hormone beta in cell culture supernates, serum, edta plasma, heparin plasma. An antibody specific for Luteinizing Hormone beta has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Luteinizing Hormone beta present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-Luteinizing Hormone beta Antibody, which binds the captured Luteinizing Hormone beta present in each well. Following incubation, unbound biotinylated detection 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 proportional to the amount of Luteinizing Hormone beta captured in each well. The concentration of Luteinizing Hormone beta can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
