首页> 外国专利> METHODS AND NUCLEIC ACID VECTORS FOR RAPID EXPRESSION AND SCREENING OF CDNA CLONES

METHODS AND NUCLEIC ACID VECTORS FOR RAPID EXPRESSION AND SCREENING OF CDNA CLONES

机译:快速表达和筛选CDNA克隆的方法和核酸载体

摘要

Recombinant DNA vectors and methods for cloning and expressing nucleic acid molecules by using a combination of site-specific recombination and end-to-end joining or linking of nucleic acid molecules, such as endonuclease restriction digestion and ligation. The DNAs, vectors and methods can be used for inserting, exchanging, transferring a variety of DNA segment (s) both in vitro and in vivo. Also disclosed are linker molecules and methods using these linkers the can be used for cloning a gene of interest into an expression vector in one-step. The linker sequences comprise adapter sequences for cloning purposes, as well as eukaryotic and prokaryotic ribosome binding sites for increase translation efficiency.
机译:通过结合位点特异性重组和核酸分子的端对端连接或连接(例如核酸内切酶限制性消化和连接)的组合,用于克隆和表达核酸分子的重组DNA载体和方法。 DNA,载体和方法可用于在体外和体内插入,交换,转移多种DNA片段。还公开了接头分子和使用这些接头的方法,其可用于一步一步将目的基因克隆到表达载体中。接头序列包含用于克隆目的的衔接子序列,以及用于提高翻译效率的真核和原核核糖体结合位点。

著录项

  • 公开/公告号EP1546395A4

    专利类型

  • 公开/公告日2007-05-02

    原文格式PDF

  • 申请/专利权人 GENECOPOEIA INC.;

    申请/专利号EP20030771868

  • 发明设计人 YANG SHUWEI;

    申请日2003-07-28

  • 分类号C12N15/10;

  • 国家 EP

  • 入库时间 2022-08-21 20:48:49

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