Sheep Fibulin ELISA Kit

fibulin 1, isoform CRA_a

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

Sheep

Competitive

Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate

1.0 ng/mL.

2192

P23142 [Other Products]