Human RAD51B(DNA repair protein RAD51 homolog 2) ELISA Kit

Biorbyt

Human RAD51B(DNA repair protein RAD51 homolog 2) ELISA Kit

10

standard: 20 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human RAD51B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RAD51B. 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 Human RAD51B, 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 Human RAD51B in the samples is then determined by comparing the OD of the samples to the standard curve

0.32-20 ng/mL

0.117 ng/mL

Research Use Only

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to DNA repair protein RAD51 homolog 2(RAD51B). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to DNA repair protein RAD51 homolog 2(RAD51B). 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 DNA repair protein RAD51 homolog 2(RAD51B), 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 DNA repair protein RAD51 homolog 2(RAD51B) in the samples is then determined by comparing the OD of the samples to the standard curve.

41116158