Catalog No.
KAH02201
Description
PRINCIPLE OF THE ASSAY This assay employs the quantitative sandwich enzyme immunoassay technique. Nivolumab has been pre-coated onto a microplate. Samples or standards are pipetted into microwells and anti-Nivolumab will be captured by immobilized Nivolumab. After washing away any unbound substances, a biotin-labeled Nivolumab 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-Nivolumab bound in the initial step. The color development is stopped and the intensity of the color is measured.
Applications
Used for the quantitative determination of Anti-Nivolumab concentration in serum and plasma.
Detection method
Colorimetric
Sample type
Plasma, Serum
Assay type
Quantitative
Range
3.13 - 200 ng/mL
Sensitivity
1.77 ng/mL
Precision
Intra-Assay Precision (Precision within an assay): <10%
Three samples of known concentration were tested sixteen times on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays): <15%
Three samples of known concentration were tested in twenty four separate assays to assess inter-assay precision.
|
|
Intra-Assay Precision |
Inter-Assay Precision |
||||
|
Sample |
1 |
2 |
3 |
1 |
2 |
3 |
|
n |
16 |
16 |
16 |
24 |
24 |
24 |
|
Mean (ng/mL) |
101.1 |
25.5 |
6.8 |
110.2 |
27.1 |
7.6 |
|
Standard deviation |
3.8 |
0.8 |
0.6 |
4.0 |
1.3 |
0.5 |
|
CV (%) |
3.7 |
3.3 |
8.1 |
3.6 |
4.6 |
6.7 |
Recovery
80-120%
Shipping
2-8 ℃
Stability and Storage
When the kit was stored at the recommended temperature for 6 months, the signal intensity decreased by less than 20%.
Alternative Names
BMS-936558,MDX-1106,ONO-4538,CAS: 946414-94-4
For research use only. Not for human or drug use.
