Principle of the Assay: LPAELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-LPAantibody and an LPA-HRP conjugate. The assay sample and buffer are incubated together with LPA-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 LPAconcentration since LPAfrom samples and LPA-HRP conjugate compete for the anti-LPAantibody binding site. Since the number of sites is limited, as more sites are occupied by LPAfrom the sample, fewer sites are left to bind LPA-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The LPAconcentration in each sample is interpolated from this standard curve.
Principle of the Assay: LPAELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-LPAantibody and an LPA-HRP conjugate. The assay sample and buffer are incubated together with LPA-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 LPAconcentration since LPAfrom samples and LPA-HRP conjugate compete for the anti-LPAantibody binding site. Since the number of sites is limited, as more sites are occupied by LPAfrom the sample, fewer sites are left to bind LPA-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The LPAconcentration in each sample is interpolated from this standard curve.