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- 详细信息
- 文献和实验
- 技术资料
- 库存:
999
- 供应商:
abinscience
- 检测范围:
1.72 - 110 ng/mL
- 检测方法:
Colorimetric
- 应用:
ELISA
- 适应物种:
Not Species Specific
- 标记物:
Unconjugated
- 样本:
Plasma, Serum
- 灵敏度:
0.38 ng/mL
- 规格:
96T

| Product name | Anti-SARS-CoV-2 RBD (BA.5) Human IgG ELISA Kit |
|---|---|
| Catalog No. | AK565018 |
| Applications | ELISA |
| Accession | \ |
| Stability and Storage | The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 10% prior to the expiration date under appropriate storage condition. |
| Detection method | Colorimetric |
| Sample type | Plasma, Serum |
| Assay type | Quantitative |
| Sensitivity | 0.38 ng/mL |
| Background | \ |
| Target | RBD (Omicron/BA.5) |
| Range | 1.72 - 110 ng/mL |
| Recovery | 80-120% |
| Alternative Names | \ |
| Clone ID | \ |
| Shipping | 2-8 ℃ |
| Note | For Research Use Only. |
Abinscience, founded in 2023 and located in the innovation technology center in Strasbourg, France, is the core research reagent brand of ProteoGenix. Focusing on the development and production of life science research reagents, Abinscience takes "Empowering Bioscience Discovery" as its vision, and is committed to providing high-quality and innovative biological reagent products and technical solutions for global researchers.
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文献和实验Kolosova A Y, Shim W B, Yang Z Y, et al. Direct competitive ELISA based on a monoclonal antibody for detection of aflatoxin B 1. Stabilization of ELISA kit components and application to grain samples[J]. Analytical and bioanalytical chemistry, 2006, 384: 286-364.
Reprogramming Fibroblasts with the CytoTune-iPS Reprogramming Kit
15. DPBS Without Calcium or Magnesium 16. TRIzol® LS Reagent 17. SuperScript® VILO™ cDNA Synthesis Kit 18. AccuPrime™ SuperMix I 19. Mouse Anti-Tra1-60 Antibody 20. Mouse Anti-Tra1-81 Antibody 21. Mouse Anti-SSEA
itself in allergic reactions, mostly caused by antibodies of the IgE-isotype, but the presence of IgG antibodies has also been described7,8. These human antibodies can then specifically interact with the blocking layer and cause persistent false positives
to a goat antimouse IgG, which catalyzes the substrate p-nitrophenyl phosphate, to form a colored product. Excess reagents are removed by washing, and enzyme activity can be measured with an ELISA plate reader at 415nm. The amount of colored product
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