- ￥580 - 5680
- 博尔森生物
- BES2P41388
- 中国/上海
- 2025年10月29日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
大量
- 英文名：
Recombinant JEV NS1 protein, N-His
- 保质期：
12个月
- 供应商：
上海博尔森生物科技有限公司
- 保存条件：
Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
- 规格：
20ul/100ul/500ul
| 规格： | 20ul | 产品价格： | ￥580.0 |
|---|---|---|---|
| 规格： | 100ul | 产品价格： | ￥1880.0 |
| 规格： | 500ul | 产品价格： | ￥5680.0 |
Recombinant JEV NS1 protein, N-His
Concentration: ＞0.5 mg/ml
AA Seq: 795-1146/3432
Predicted MW: 40
Detected MW: 46 kDa
Tags: N-His
Activity: Not tested
Endotoxin: Not analyzed
Purity: >90% as determined by SDS-PAGE
Purification: AC
Form: Lyophilized or Liquid
Storage: 4M Urea (pH7.5) with 1mM DDT.
Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
Background: Involved in immune evasion, pathogenesis and viral replication. Once cleaved off the polyprotein, is targeted to three destinations: the viral replication cycle, the plasma membrane and the extracellular compartment. Essential for viral replication. Required for formation of the replication complex and recruitment of other non-structural proteins to the ER-derived membrane structures. Excreted as a hexameric lipoparticle that plays a role against host immune response. Antagonizing the complement function. Binds to the host macrophages and dendritic cells. Inhibits signal transduction originating from Toll-like receptor 3 (TLR3).
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文献和实验Recombinant DNA Engineering, Or Cloning Genes In Plasmids
and thus fusion proteins. For example there might be sequence for a fluorescent protein such as GFP or a peptide tag such as HA upstream of MCS (and downstream of promoter) so that an insert in frame will lead to the generation of a fusion protein, an N-terminal
, and usually final protein yield between 0.1 and 2 mg/g cells is acceptable. Another concern is protein degradation. Especially with Pichia , protease activity during cell lysis and purification is always an issue. The importance of N-terminal degradation
The Use of Recombinant Fusion Proteases in the Affinity Purification of Recombinant Proteins
of interest, but some affinity tails are able to be linked to either the N- or C-terminus of the protein of interest. The choice of affinity tail to use for the expression of any particular protein is empirical since the factors leading to the high expression of recombinant
