Description
Principle of the assay: DNM2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-DNM2 antibody and an DNM2-HRP conjugate. The assay sample and buffer are incubated together with DNM2-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the DNM2 concentration since DNM2 from samples and DNM2-HRP conjugate compete for the anti-DNM2 antibody binding site. Since the number of sites is limited, as more sites are occupied by DNM2 from the sample, fewer sites are left to bind DNM2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The DNM2 concentration in each sample is interpolated from this standard curve