Description
Principle of the Assay: Histone-H2b ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for Histone-H2b. Standards or samples are then added to the microtiter plate wells and Histone-H2b if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of Histone-H2b present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for Histone-H2b are added to each well to "sandwich" the Histone-H2b immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain Histone-H2b and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Histone-H2b concentration in each sample is interpolated from this standard curve