Human MR-ProADM(Mid-regional pro-adrenomedullin) ELISA Kit

Biorbyt

Human MR-ProADM(Mid-regional pro-adrenomedullin) ELISA Kit

10

standard: 1000 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 MR-ProADM. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MR-ProADM. 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 MR-ProADM, 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 MR-ProADM in the samples is then determined by comparing the OD of the samples to the standard curve

15.63-1000 pg/mL

9.17 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 Mid-regional pro-adrenomedullin(MR-ProADM). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Mid-regional pro-adrenomedullin(MR-ProADM). 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 Mid-regional pro-adrenomedullin(MR-ProADM), 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 Mid-regional pro-adrenomedullin(MR-ProADM) in the samples is then determined by comparing the OD of the samples to the standard curve.

Human

41116158