Human PDE9A ELISA Kit

Biorbyt

Human PDE9A ELISA Kit

10

standard: 10 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 PDE9A. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human PDE9A. 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 PDE9A, 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 PDE9A in the samples is then determined by comparing the OD of the samples to the standard curve

ELISA

ELISA

0.16-10 ng/mL

0.052 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 High affinity cGMP-specific 3,5-cyclic phosphodiesterase 9A(PDE9A). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to High affinity cGMP-specific 3,5-cyclic phosphodiesterase 9A(PDE9A). 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 High affinity cGMP-specific 3,5-cyclic phosphodiesterase 9A(PDE9A), 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 High affinity cGMP-specific 3,5-cyclic phosphodiesterase 9A(PDE9A) in the samples is then determined by comparing the OD of the samples to the standard curve.

Human

41116158