- ￥1338 - 9188
- abinScience
- France
- VK560023
- 2026年04月26日
- ELISA: 1:2000-1:20000
- Alpaca
- Influenza A virus
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- 详细信息
- 文献和实验
- 技术资料
- 亚型：
VHH-His
- 形态：
Liquid
- 保存条件：
-20°C
- 克隆性：
单克隆
- 适应物种：
Influenza A virus
- 保质期：
twelve months
- 级别：
一抗
- 供应商：
武汉益普生物科技有限公司
- 宿主：
Alpaca
- 应用范围：
ELISA: 1:2000-1:20000
- 抗体英文名：
Anti-Influenza A virus RNA polymerase complex Nanobody (SAA2270)
- 规格：
50μg/100μg/1mg
| 规格： | 50μg | 产品价格： | ￥1338.0 |
|---|---|---|---|
| 规格： | 100μg | 产品价格： | ￥2288.0 |
| 规格： | 1mg | 产品价格： | ￥9188.0 |
| 产品名 | Anti-Influenza A virus RNA polymerase complex Nanobody (SAA2270) |
| 货号 | VK560023 |
| 宿主 | Alpaca |
| 种属反应性 | Influenza A virus |
| 克隆类型 | Monoclonal |
| 克隆号 | SAA2270 |
| Accession号 | P03427 |
| 靶标 | Polymerase acidic protein, RNA-directed RNA polymerase subunit P2, PA |
| 同种型 | VHH-His |
| 应用 | ELISA |
| 应用范围 | ELISA: 1:2000-1:20000 |
| 内毒素水平 | Please contact with the lab for this information. |
| 纯化方式 | Protein A/G purified from cell culture supernatant. |
| 纯度 | >90% as determined by SDS-PAGE. |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4. |
| 稳定性和存储 | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. |
| 说明 | For research use only. |
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文献和实验Avian Influenza Virus RNA Extraction from Tissue and Swab Material
, are the most difficult to process due to the complex sample composition and possibly low virus titers. In this chapter, two well-established procedures for the isolation of AI virus RNA from common clinical specimen types and enriched virus stocks for further molecular
Reverse Genetics of the Avian Influenza Virus
viral RNAs. Although slightly different methods are being used in different laboratories for the rescue of the influenza virus, the basic concept of synthesizing viral RNA using RNA polymerase I remains the same. Coupled with in vitro mutagenesis
Influenza A Virus Molecular Virology Techniques
influenza A viruses by plasmid-based reverse genetics. To accelerate the amplification and cloning process, we developed multi-segment-RTPCR (M-RTPCR) techniques that efficiently amplify the eight genomic viral RNA segments (vRNAs) of influenza A virus
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