Human LONP1(Lon protease homolog, mitochondrial) ELISA Kit

Biorbyt

Human LONP1(Lon protease homolog, mitochondrial) ELISA Kit

10

standard: 2000 pg/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 LONP1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LONP1. 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 LONP1, 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 LONP1 in the samples is then determined by comparing the OD of the samples to the standard curve

31.25-2000 pg/mL

12.2 pg/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 Lon protease homolog, mitochondrial(LONP1). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Lon protease homolog, mitochondrial(LONP1). 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 Lon protease homolog, mitochondrial(LONP1), 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 Lon protease homolog, mitochondrial(LONP1) in the samples is then determined by comparing the OD of the samples to the standard curve.

Human

41116158