Principle of Assay
Human MBD2 ELISA Kit (A303367) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human MBD2 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for MBD2 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MBD2 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-MBD2 Antibody, which binds the captured MBD2 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 MBD2 captured in each well. The concentration of MBD2 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
