Human UTS2B ELISA Kit (A311288) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human UTS2B in An antibody specific for UTS2B has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the UTS2B present in each sample is bound to the wells by the immobilized antibody. Biotinylated Anti-UTS2B Antibody, which also binds the UTS2B present in each sample, and Streptavidin-HRP, which binds the Biotinylated Anti-UTS2B Antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated Anti-UTS2B Antibody and unbound Streptavidin-HRP are removed by washing, and two substrate solutions are added to the wells. Color develops in proportion to the amount of UTS2B captured in each well. The color development is stopped by addition of stop solution which changes the color from blue to yellow and the intensity of the color is then measured. The concentration of UTS2B in the samples can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.