- ￥2588 - 9188
- 泽叶生物
- BES2416mAb
- 中国/上海
- 2026年01月30日
- ELISA, Neutralization
- Human
- 详见操作说明
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- 详细信息
- 文献和实验
- 技术资料
- 抗体名：
InVivoMAb Anti-Nipah virus/NiV Glycoprotein G Antibody (SAA2192)
- 抗体英文名：
InVivoMAb Anti-Nipah virus/NiV Glycoprotein G Antibody (SAA2192)
- 靶点：
详见操作说明
- 浓度：
详见操作说明
- 应用范围：
ELISA, Neutralization
- 宿主：
Human
- 供应商：
上海泽叶生物科技有限公司
- 库存：
大量
- 级别：
详见操作说明
- 抗原来源：
详见操作说明
- 保质期：
详见操作说明
- 适应物种：
详见操作说明
- 标记物：
详见操作说明
- 克隆性：
单克隆
- 保存条件：
常温/干冰
- 形态：
液体
- 亚型：
详见操作说明
- 免疫原：
详见操作说明
- 规格：
100ug/1mg
| 规格： | 100ug | 产品价格： | ￥2588.0 |
|---|---|---|---|
| 规格： | 1mg | 产品价格： | ￥9188.0 |
InVivoMAb Anti-Nipah virus/NiV Glycoprotein G Antibody (SAA2192)
货号：BES2416mAb
品牌：博尔森生物
描述：InVivoMAb Anti-Nipah virus/NiV Glycoprotein G Antibody (SAA2192) [SAA2192] is a human monoclonal antibody detecting Glycoprotein G in ELISA, Neutralization. Suitable for Nipah virus (NiV).
种属反应性：Nipah virus (NiV)
应用：ELISA, Neutralization
宿主：Human
同种型：IgG1
克隆号：SAA2192
克隆类型：Monoclonal
靶标：Glycoprotein G, G
内毒素水平：Please contact with the lab for this information.
纯度：>95% as determined by SDS-PAGE.
纯化方式：Protein A/G purified from cell culture supernatant.
Accession号：Q9IH62
状态：Liquid
保存溶液：0.01M PBS, pH 7.4.
Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA.
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.
Note：For research use only. Not suitable for clinical or therapeutic use.
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文献和实验Hematopoietic Stem Cell Targeting with Surface-Engineered Lentiviral Vectors
an HIV-1-derived self-inactivating vector with the internal EF1- promoter driving the green fluorescent protein (GFP) reporter gene Envelope glycoprotein-expressing plasmids Fusion glycoprotein: VSV-G
PCR引物设计和优化(PCR PRIMER DESIGN AND REACTION OPTIMISATION)
The specific complementary ass℃iation due to hydrogen bonding of single-stranded nucleic acids is referred to as "annealing": two complementary sequences will form hydrogen bonds between their complementary bases (G to C, and A to T or U) and form
一、文献 1. Chen, H.H., J. Lebon, and A.D. Riggs, Analysis of RNA structure and RNA-protein interactions in mammalian cells by use of terminal transferase-dependent PCR. Methods Mol Biol, 2008. 488: p. 319-41. 2. Terzi, L.C. and G.G. Simpson
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