Assay Type: Competitive Inhibition. Assay length: 2h. Research Area: Glycolipid metabolism. Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human NES1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NES1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm 10nm. The concentration of Human NES1 in the samples is then determined by comparing the OD of the samples to the standard curve
ELK2828
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