Catalog No.
KAC90701
Description
PRINCIPLE OF THE ASSAY This assay employs the quantitative sandwich enzyme immunoassay technique. Rituximab has been pre-coated onto a microplate. Samples or standards are pipetted into microwells and Anti-Rituximab will be captured by immobilized Rituximab. After washing away any unbound substances, a biotin-labeled Rituximab 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-Rituximab 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-Rituximab concentration in serum and plasma.
Detection method
Colorimetric
Sample type
Plasma, Serum
Assay type
Quantitative
Range
1.25 - 80 ng/mL
Sensitivity
0.89 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) |
32.1 |
8.6 |
2.1 |
32.2 |
8.8 |
2.4 |
Standard deviation |
0.8 |
0.2 |
0.1 |
1.7 |
0.3 |
0.2 |
CV (%) |
2.5 |
2.3 |
4.2 |
5.1 |
3.0 |
8.1 |
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
IDEC-C2B8,CAS: 174722-31-7