Description
Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with HBV preS2Ab. Samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP) -conjugated HBV preS2Ab and incubated. Then substrate solutions are 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. Calculate the valence of HBV preS2Ag in the samples