Adenosine A2b Receptor (ADORA2b) ELISA Kit for Mouse

Test Principle: The microtiter plate provided in this kit has been pre-coated with an antibody specific to ADORA2b. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific to ADORA2b. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain ADORA2b, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of ADORA2b in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Small volumes of ADORA2b 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.

MBS457427 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Adenosine A2b Receptor (ADORA2b) 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 ADORA2b. The ELISA analytical biochemical technique of the MBS457427 kit is based on ADORA2b antibody-ADORA2b antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect ADORA2b antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, ADORA2b. 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(%).