Alcohol Dehydrogenase 1 (ADH1) ELISA Kit for Porcine

Principle of the Assay: ADH1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-ADH1 antibody and an ADH1-HRP conjugate. The assay sample and buffer are incubated together with ADH1-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 ADH1 concentration since ADH1 from samples and ADH1-HRP conjugate compete for the anti-ADH1 antibody binding site. Since the number of sites is limited, as more sites are occupied by ADH1 from the sample, fewer sites are left to bind ADH1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ADH1 concentration in each sample is interpolated from this standard curve.

Small volumes of ADH1 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS736593 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Alcohol Dehydrogenase 1 (ADH1) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing ADH1. The ELISA analytical biochemical technique of the MBS736593 kit is based on ADH1 antibody-ADH1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect ADH1 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, ADH1. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).