Horse KL(Klotho) ELISA Kit
ORB1146775
ReactivityEquine
Product group Assays
Overview
- SupplierBiorbyt
- Product NameHorse KL(Klotho) ELISA Kit
- Delivery Days Customer10
- Application Supplier Notestandard: 20 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 KL. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse KL. 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 KL, 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 KL in the samples is then determined by comparing the OD of the samples to the standard curve
- Assay Detection Range0.32-20 ng/mL
- Assay Sensitivity0.117 ng/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 Klotho(KL). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Klotho(KL). 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 Klotho(KL), 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 Klotho(KL) in the samples is then determined by comparing the OD of the samples to the standard curve.
- ReactivityEquine
- UNSPSC41116158


