Creatine Kinase S-Type (CKMT2) ELISA Kit for Mouse

Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate CKMT2 in Mouse serum, plasma, tissue homogenates. An antibody specific for CKMT2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any CKMT2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for CKMT2 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of CKMT2 bound in the initial step. The color development is stopped and the intensity of the color is measured.

Intended Uses: For the quantitative detection of Mouse Creatine kinase S-type, mitochondrial (CKMT2) concentration in serum, plasma, tissue homogenates and other biological fluids.

Small volumes of CKMT2 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.

MBS285126 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Creatine kinase S-type (CKMT2) 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 CKMT2. The ELISA analytical biochemical technique of the MBS285126 kit is based on CKMT2 antibody-CKMT2 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect CKMT2 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, CKMT2. 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(%).