This Human ATP-dependent zinc metalloprotease YME1L1 (YME1L1) ELISA Kit employs a two-site sandwich ELISA to quantitate YME1L1 in samples. An antibody specific for YME1L1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyYME1L1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for YME1L1 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 YME1L1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
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