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제품 설명
Anti-Bevacizumab ELISA Kit
제품 번호
KAD12601
제품 특징
KAD12601
PRINCIPLE OF THE ASSAY This assay employs the quantitative sandwich enzyme immunoassay technique. Bevacizumab has been pre-coated onto a microplate. Samples or standards are pipetted into microwells and Anti-Bevacizumab will be captured by immobilized Bevacizumab. After washing away any unbound substances, a biotin-labeled Bevacizumab 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-Bevacizumab bound in the initial step. The color development is stopped and the intensity of the color is measured.
Used for the quantitative determination of Anti-Bevacizumab concentration in serum and plasma.
Colorimetric
Plasma, Serum
Quantitative
9.38 - 600 ng/mL
5.78 ng/mL
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) | 290.2 | 71.3 | 15.2 | 294.6 | 72.8 | 15.5 |
Standard deviation | 8.9 | 2.4 | 1.3 | 6.8 | 2.3 | 1.7 |
CV (%) | 3.1 | 3.4 | 8.7 | 2.3 | 3.2 | 11.1 |
80-120%
2-8 ℃
When the kit was stored at the recommended temperature for 6 months, the signal intensity decreased by less than 20%.
12-IgG1,F(ab)-12 IgG1,Fab-12 IgG1,rhuMAb-VEGF, ABP 215,CAS: 216974-75-3
Data Image
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