Mannose Phosphate Isomerase (MPI) ELISA Kit for Human

Intended Uses: This sandwich kit is for the accurate quantitative detection of human Mannose Phosphate Isomerase (also known as MPI) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.

Principles of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with human MPI antibody. MPI present in the sample is added and binds to antibodies coated on the wells. And then biotinylated human MPI Antibody is added and binds to MPI in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated MPI antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of human MPI. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.

Small volumes of MPI 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.

MBS167596 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Mannose Phosphate Isomerase (MPI) 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 MPI. The ELISA analytical biochemical technique of the MBS167596 kit is based on MPI antibody-MPI antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect MPI antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, MPI. 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(%).