Bovine 2,3- Bisphosphoglycerate, 2,3 -DPG ELISA Kit
96 Tests
Operating instructions
FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE
BEGINNING!
Synonyms
2,3-Bisphosphoglycerate,2,3-Bisphosphoglyceric acid,2,3-diphosphoglycerate,2,3-BPG, 2,3-DPG
Search name
Bovine 2,3-Bisphosphoglycerate ELISA Kit, Bovine 2,3-BPG ELISA Kit, Bovine 2,3-Bisphosphoglyceric acid ELISA Kit,
Bovine 2,3-diphosphoglycerate ELISA Kit, Bovine 2,3-DPG ELISA Kit
Intended use
This immunoassay kit allows for the in vitro quantitative determination of Bovine 2,3-Bisphosphoglycerate concentrations in serum,
plasma, tissue homogenates, cell culture supernates, and other biological fluids.
Test principle
The ELISA is based on the competitive binding enzyme immunoassay technique. The microtiter plate provided in this kit has been
pre-coated with an antibody specific to 2,3-Bisphosphoglycerate, During the reaction, 2,3-Bisphosphoglycerate in the sample or standard
competes with a fixed amount of biotin-labeled 2,3-Bisphosphoglycerate for sites on a pre-coated Monoclonal antibody specific to
2,3-Bisphosphoglycerate. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to
Horseradish Peroxidase (HRP) 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 ± 2 nm. The concentration of 2,3-Bisphosphoglycerate in the samples is then
determined by comparing the O.D. of the samples to the standard curve.
Technical Principle & Methodology
The quality assurance and experimental performance of this biological reagent are rigorously optimized and standardized according to its specific technical pathway:
Double Antibody Sandwich Method
(双抗体夹心法). This ensures maximum reproducibility across clinical research and scientific workflows.
