Horse FABP7(Fatty Acid Binding Protein 7, Brain) ELISA Kit

Biorbyt

Horse FABP7(Fatty Acid Binding Protein 7, Brain) ELISA Kit

10

standard: 30 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 Horse FABP7. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse FABP7. 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 Horse FABP7, 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 Horse FABP7 in the samples is then determined by comparing the OD of the samples to the standard curve

0.47-30 ng/mL

0.18 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 Fatty Acid Binding Protein 7, Brain(FABP7). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Fatty Acid Binding Protein 7, Brain(FABP7). 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 Fatty Acid Binding Protein 7, Brain(FABP7), 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 Fatty Acid Binding Protein 7, Brain(FABP7) in the samples is then determined by comparing the OD of the samples to the standard curve.

Equine

41116158