Total Leukotriene (LT) ELISA Kit for Canine

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

Small volumes of LT 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.

MBS750466 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Total Leukotriene (LT) 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 LT. The ELISA analytical biochemical technique of the MBS750466 kit is based on LT antibody-LT antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect LT antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, LT. 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(%).