Description
This assay employs a two-site sandwich ELISA to quantitate LOW-ADP in samples. An antibody specific for LOW-ADP has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any LOW-ADP present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for LOW-ADP is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of LOW-ADP bound in the initial step. The color development is stopped and the intensity of the color is measured