Principle of Assay
Human SLC10A2/ASBT ELISA Kit (A303176) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human SLC10A2/ASBT in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for SLC10A2/ASBT. Standards and samples are added to the wells, where SLC10A2/ASBT binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for SLC10A2/ASBT is added to the wells. The detection antibody binds the captured SLC10A2/ASBT 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 SLC10A2/ASBT captured in each well. The concentration of SLC10A2/ASBT is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.