Oxidized Lowdensity Lipoprotein Antibody, Olab ELISA Kit for Human

Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with oxidized low density lipoprotein. Standards and samples are pipetted into the wells with a biotin-conjugated oxidized low density lipoprotein and avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound reagent, a substrate solution is added to the wells and color develops in proportion to the amount of OLAb bound in the initial step. The color development is stopped and the intensity of the color is measured.

Small volumes of oxidized lowdensity lipoprotein antibody, OLAb 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.

MBS704155 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the oxidized lowdensity lipoprotein antibody, OLAb, 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 oxidized lowdensity lipoprotein antibody, OLAb. The ELISA analytical biochemical technique of the MBS704155 kit is based on oxidized lowdensity lipoprotein antibody, OLAb antibody-oxidized lowdensity lipoprotein antibody, OLAb antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect oxidized lowdensity lipoprotein antibody, OLAb antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, oxidized lowdensity lipoprotein antibody, OLAb. 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(%).