货号 | 产品名称 | 规格 | 库存 | 价格 | 数量 | 购买 |
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KL-ZL-0136-01 | pET-44a 质粒 | NA |
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产品名称:pET-44a 质粒
货号:KL-ZL-0136
详细描述:
启动子: | T7/lac |
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复制子: | ColE1 ori,F1 ori |
终止子: | T7 terminator |
质粒分类: | 大肠杆菌载体;PET系列表达质粒 |
质粒大小: | 7311bp |
质粒标签: | C-HSV, N-6×His, C-6×His, N-Thrombin, N-Nus, N-EK |
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: | T7:TAATACGACTCACTATAGGG |
3'测序引物: | T7-ter:TGCTAGTTATTGCTCAGCGG |
产地:美国,中国
质粒简介:
The pET-44 vectors are designed for cloning and high-level expression of peptide sequences fused with the 495 aa Nus•Tag™ protein. Compared to the pET-43.1 series, the pET-44 vectors encode an additional N-terminal His•Tag. Unique sites are shown on the circle map. Note that the sequence is numbered by the pBR322 convention, so the T7 expression region is reversed on the circle map. The cloning/expression region of the coding strand transcribed by T7 RNA polymerase is shown below. The f1 origin is oriented so that infection with helper phage will produce virions containing single stranded DNA that corresponds to the coding strand. Therefore, single stranded sequencing should be performed using the COLIDOWN primer (Cat. No. 70845-3). Vector encoded sequence can be completely removed when cloning into the PshA I or Sma I sites (as shown below) by cleaving the Nus•Tag fusion protein with enterokinase or thrombin, respectively.