Remnant Lipoprotein - Cholesterol (RLP-C) ELISA Kit for Rabbit

Background: This Quantitative Sandwich ELISA kit is only for in vitro research use only! It is intended to be determinated RLP-C concentrations in Rabbit serum, plasma and other body fluids. Using Purified Rabbit RLP-C antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add RLP-C and RLP-C antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of RLP-C in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Small volumes of RLP-C 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.

MBS046490 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Remnant Lipoprotein - Cholesterol (RLP-C) 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 RLP-C. The ELISA analytical biochemical technique of the MBS046490 kit is based on RLP-C antibody-RLP-C antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect RLP-C antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, RLP-C. 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(%).