生物
科尔1
质粒
复制子
多克隆站点
克隆载体
克隆(编程)
重组DNA
遗传学
T-DNA二元系统
转化(遗传学)
分子克隆
基因
穿梭机载体
大肠杆菌
载体(分子生物学)
计算生物学
肽序列
程序设计语言
计算机科学
作者
Michael E. Kovach,Philip H. Elzer,D. Steven Hill,Gregory T. Robertson,Michael A. Farris,R. Martin Roop,Kenneth M. Peterson
出处
期刊:Gene
[Elsevier]
日期:1995-12-01
卷期号:166 (1): 175-176
被引量:3316
标识
DOI:10.1016/0378-1119(95)00584-1
摘要
Four new antibiotic-resistant derivatives of the broad-host-range (bhr) cloning vector pBBR1MCS have been constructed. These new plasmids have several advantages over many of the currently available bhr vectors in that: (i) they are relatively small (< 5.3 kb), (ii) they possess an extended multiple cloning site (MCS), (iii) they allow direct selection of recombinant plasmid molecules in Escherichia coli via disruption of the LacZ alpha peptide, (iv) they are mobilizable when the RK2 transfer functions are provided in trans and (v) they are compatible with IncP, IncQ and IncW group plasmids, as well as with ColE1- and P15a-based replicons.
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