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- 详细信息
- 文献和实验
- 技术资料
- 亚型:
IgG1, kappa
- 形态:
Liquid
- 保存条件:
-20°C
- 克隆性:
单克隆
- 适应物种:
West Nile virus (strain NY-99) (WNV) (West Nile virus (strain NY-1999))
- 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:
Human
- 应用范围:
ELISA: 1:2000-1:20000; WB: 1:500-1:2000
- 抗体英文名:
Anti-West Nile virus/WNV GP1/Genome polyprotein Antibody (CR4274)
- 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: | ¥11148.0 |
| 产品名 | Anti-West Nile virus/WNV GP1/Genome polyprotein Antibody (CR4274) |
| 货号 | VK554033 |
| 宿主 | Human |
| 种属反应性 | West Nile virus (strain NY-99) (WNV) (West Nile virus (strain NY-1999)) |
| 克隆类型 | Monoclonal |
| 克隆号 | CR4274 |
| Accession号 | Q9Q6P4 |
| 靶标 | Genome polyprotein, Peptide 2k, Capsid protein C, Core protein, Protein prM, Peptide pr, Small envelope protein M, Matrix protein, Envelope protein E, Non-structural protein 1, NS1, Non-structural protein 2A, NS2A, Serine protease subunit NS2B, Flavivirin protease NS2B regulatory subunit, Non-structural protein 2B, Serine protease/Helicase NS3, 3.4.21.91, 3.6.1.15, 3.6.4.13, Flavivirin protease NS3 catalytic subunit, Non-structural protein 3, Non-structural protein 4A, NS4A, Non-structural protein 4B, NS4B, RNA-directed RNA polymerase NS5, 2.1.1.56, 2.1.1.57, 2.7.7.48, NS5, GP1, MZ11_60484gpGP1, MZ11_60553gpGP1 |
| 同种型 | IgG1, kappa |
| 应用 | ELISA, SPR, WB |
| 应用范围 | ELISA: 1:2000-1:20000; WB: 1:500-1:2000 |
| 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 | >95% 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 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| 说明 | For research use only. |

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文献和实验Propagation, Quantification, Detection, and Storage of West Nile Virus
Abstract Table of Contents Materials Figures Literature Cited Abstract West Nile virus (WNV
for studying the effects of mutations in translation and/or replication in isolation from processes like the entry and assembly of the virus particles. Here we describe the construction of two West Nile virus (WNV) replicons by overlap extension PCR
associated with a given protein. The RNP immunoprecipitation (RIP) assay was developed using RNA–protein interactions of hepatitis delta virus (HDV) as a model system. HDV is an RNA virus with a single-stranded circular RNA genome that encodes one viral
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