- ￥3510 - 25389
- Biorbyt
- 英国
- orb2962188
- 2026年08月06日
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- 文献和实验
- 技术资料
- 保存条件：
详询
- 保质期：
6 months from date of receipt.
- 英文名：
Recombinant JUNV GP2 Protein, N-His
- 库存：
99
- 供应商：
Biorbyt
- 规格：
50 ug/100 ug/1 mg
| 规格： | 50 ug | 产品价格： | ￥3510.0 |
|---|---|---|---|
| 规格： | 100 ug | 产品价格： | ￥5148.0 |
| 规格： | 1 mg | 产品价格： | ￥25389.0 |
描述: Recombinant JUNV GP2 Protein, N-His is produced in E. coli and supplied in lyophilized form. The protein includes the regions of Ala252-Asp424 and carries the N-His tag. With a molecular weight of 22.32 kDa, it is suitable for ELISA, SDS-PAGE and WB applications. This product is lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% trehalose, 1% mannitol and has a purity of greater than 90% as determined by SDS-PAGE.
别名: Pre-glycoprotein polyprotein GP complex, Glycoprotein G2, GP2, GPC, GP-C
形态: Lyophilized
应用: ELISA, SDS-PAGE, WB
生物来源: Junin mammarenavirus (JUNV) (Junn mammarenavirus)
内毒素: Please contact with the lab for this information.
表达区域: Ala252-Asp424
表达系统: E. coli
分子量: 22.32 kDa
防腐剂: Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
蛋白长度: Ala252-Asp424
纯度: >90% as determined by SDS-PAGE.
复溶/重构: Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
研究领域: Immunology & Inflammation
UniProt ID: P26313
保存条件: -20°C
备注: For research use only.
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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
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