This Human N-alpha-acetyltransferase 50, NatE catalytic subunit (NAT13) ELISA Kit employs a two-site sandwich ELISA to quantitate NAT13 in samples. An antibody specific for NAT13 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyNAT13 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for NAT13 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 NAT13 bound in the initial step. The color development is stopped and the intensity of the color is measured.
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