IgA-Inducing Protein Homolog (IGIP) ELISA Kit for Human

Principle of the Assay||This ELISA kit uses Competitive-ELISA as the method. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human IGIP. During the reaction,Human IGIP in the sample or standard competes with a fixed amount of biotin-labeled Human IGIP for sites on a pre-coated Monoclonal antibody specific to Human IGIP. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate 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 Human IGIP in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Small volumes of IGIP 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.

MBS765054 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the IgA-inducing protein homolog (IGIP) 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 IGIP. The ELISA analytical biochemical technique of the MBS765054 kit is based on IGIP antibody-IGIP antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect IGIP antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, IGIP. 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(%).