Human Blood group antigen-binding adhesin A (Bab A) ELISA Kit employs a two-site sandwich ELISA to quantitate Bab A in samples. An antibody specific for Human Bab A has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any Bab A present is bound by the immobilized antibody. After removing any unbound substances, HRP-Conjugated Bab A detection antibody is added to the wells. Following a wash to remove any unbound HRP reagent, a Chromogen solution is added to the wells and color develops in proportion to the amount of Bab A bound in the initial step. The color development is stopped and the intensity of the color is measured.
* VAT and and shipping costs not included. Errors and price changes excepted
