This Human Double-strand break repair protein MRE11A (MRE11A) ELISA Kit employs a two-site sandwich ELISA to quantitate MRE11A in samples. An antibody specific for MRE11A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMRE11A present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for MRE11A 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 MRE11A bound in the initial step. The color development is stopped and the intensity of the color is measured.
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