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一类与pBR322及其衍生物兼容的源自pACYC184的克隆载体的构建及特性

Construction and properties of a family of pACYC184-derived cloning vectors compatible with pBR322 and its derivatives.

作者信息

Bartolomé B, Jubete Y, Martínez E, de la Cruz F

机构信息

Departamento de Biología Molecular, Universidad de Cantabria, Santander, Spain.

出版信息

Gene. 1991 Jun 15;102(1):75-8. doi: 10.1016/0378-1119(91)90541-i.

DOI:10.1016/0378-1119(91)90541-i
PMID:1840539
Abstract

A family of cloning vectors derived from plasmid pACYC184 and, therefore, compatible with pBR322 and its derivatives (especially the pUC family of vectors), is described. They all contain a multiple cloning site (MCS) and the lacZ alpha reporter gene for easy cloning. They have been grouped in three sets: (i) six of the vectors contain a chloramphenicol-resistance (CmR)-encoding gene and each a different MCS with 16 unique restriction sites overall; (ii) another six vectors contain a kanamycin-resistance (KmR)-encoding gene and the same six MCS; and (iii) two CmR vectors that contain the SP6 and T7 promoters flanking the MCS and lacZ alpha reporter gene of pUC18/19.

摘要

本文描述了一类源自质粒pACYC184的克隆载体家族,因此与pBR322及其衍生物(特别是pUC载体家族)兼容。它们都含有一个多克隆位点(MCS)和用于便于克隆的lacZα报告基因。它们被分为三组:(i)六个载体含有氯霉素抗性(CmR)编码基因,每个载体有不同的MCS,总共16个独特的限制性酶切位点;(ii)另外六个载体含有卡那霉素抗性(KmR)编码基因和相同的六个MCS;以及(iii)两个CmR载体,其在pUC18/19的MCS和lacZα报告基因两侧含有SP6和T7启动子。

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