Principle of Assay
Human MADH7/SMAD7 ELISA Kit (A73957) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human MADH7/SMAD7 in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for MADH7/SMAD7. Standards and samples are added to the wells, where MADH7/SMAD7 binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for MADH7/SMAD7 is added to the wells. The detection antibody binds the captured MADH7/SMAD7 to form an antibody-antigen-antibody sandwich complex. After further incubation and washing, HRP-Streptavidin conjugate is added to the wells. TMB substrate solution is then added to visualize the HRP enzymatic reaction. This produces a blue-coloured product that changes to yellow following addition of acidic stop solution. The intensity of the yellow colour is directly proportional to the amount of MADH7/SMAD7 captured in each well. The concentration of MADH7/SMAD7 is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.