货号 | 产品名称 | 规格 | 库存 | 价格 | 数量 | 购买 |
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kl-zl-0661-01 | pMal-p5X质粒 | NA |
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pMal-p5X质粒 货号:kl-zl-0661 规格:20ul
启动子: | Tac |
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复制子: | ColE1 ori |
终止子: | rrnB T1 terminator |
质粒分类: | 大肠杆菌载体;pMal系列表达质粒 |
质粒大小: | 5752bp |
质粒标签: | N-MBP |
原核抗性: | 氨苄青霉素Amp |
克隆菌株: | DH5α |
培养条件: | 37℃,有氧,LB |
表达宿主: | BL21(DE3) |
诱导方式: | IPTG或乳糖及其类似物 |
5'测序引物: | 根据序列设计 |
3'测序引物: | 根据序列设计 |
备注: | 融合表达麦芽糖结合蛋白MBP,蛋白定位于细胞周质 |
The vector pMAL-p5X is designed to produce maltose-binding protein (MBP) fusions, where the protein of interest can be cleaved from MBP with the specific protease Factor Xa (NEB #P8010).
MBP fusions made with this vector include an N-terminal signal sequence, so the fusion protein is directed to the periplasm. The MBP has been engineered for tighter binding to amylose resin.
A gene or open reading frame is inserted into a restriction site of the vector polylinker, in the same translational reading frame as themalEgene (encoding maltose-binding protein). The fusion protein thus produced can be purified by amylose affinity chromatography. The sequence coding for the four amino acids Ile-Glu-Gly-Arg is present just upstream of the XmnI site. This allows the protein of interest to be cleaved from maltose-binding protein with the specific protease Factor Xa. Fragments inserted in the XmnI site (cleaves GAAGG↓ATTTC) will produce a fusion protein that, after Factor Xa cleavage, contains no vector-derived residues on the protein of interest.
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