Human RLN2(Relaxin 2) ELISA Kit
ORB1088165
Product group Assays
Overview
- SupplierBiorbyt
- Product NameHuman RLN2(Relaxin 2) ELISA Kit
- Delivery Days Customer10
- Application Supplier Notestandard: 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 RLN2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human RLN2. 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 RLN2, 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 RLN2 in the samples is then determined by comparing the OD of the samples to the standard curve
- Assay Detection Range31.25-2000 pg/mL
- Assay Sensitivity8.52 pg/mL
- CertificationResearch Use Only
- Scientific DescriptionThe 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 Relaxin 2(RLN2). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Relaxin 2(RLN2). 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 Relaxin 2(RLN2), 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 Relaxin 2(RLN2) in the samples is then determined by comparing the OD of the samples to the standard curve.
- UNSPSC41116158

