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pMal-p5X质粒

  • 货号:kl-zl-0661-01
货号 产品名称 规格 库存 价格 数量 购买
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
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
质粒简介:

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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