Description
Principle of the assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for DLL1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any DLL1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for DLL1 is added to the wells. After washing, avidin 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 DLL1 bound in the initial step. The color development is stopped and the intensity of the color is measured