PRINCIPLE OF THE ASSAY
This assay employs the quantitative sandwich enzyme immunoassay technique. Tiragolumab has been pre-coated onto a microplate. Samples or standards are pipetted into microwells and anti-Tiragolumab will be captured by immobilized Tiragolumab. After washing away any unbound substances, a biotin-labeled Tiragolumab is added to the wells. After washing away any unbound substances, Streptavidin-HRP is added to the wells. Following a wash to remove any unbound enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of Anti-Tiragolumab bound in the initial step. The color development is stopped and the intensity of the color is measured.
Stability and Storage | When the kit was stored at the recommended temperature for 6 months, the signal intensity decreased by less than 20%. For unopened kits, if you want to prolong the storage time, please store the Standard, Detection A, Detection B and Microplate at - 20℃, the rest reagents should be store at 4℃. |
Detection method | Colorimetric |
Sample type | Plasma, Serum |
Assay type | Quantitative |
Sensitivity | 10.11 ng/mL |
Range | 156.25 - 10,000 ng/mL |
Recovery | 80-120% |
Background | |
Alternative Names | MTIG-7192-A, MTIG-7192A, MTIG7192A, RG-6058, RO-7092284, RO7092284,CAS: 1918185-84-8 |
Shipping | 2-8 ℃ |
Specifications | Tiragolumab |
Note | For Research Use Only. |