首页> 外国专利> CLONING VECTOR PLASMID, VECTOR PRIMER DERIVED FROM THE SAME PLASMID AND PREPARATION OF CDNA BANK USING THE SAME PRIMER

CLONING VECTOR PLASMID, VECTOR PRIMER DERIVED FROM THE SAME PLASMID AND PREPARATION OF CDNA BANK USING THE SAME PRIMER

机译:复制质粒,从相同质粒衍生的向量底漆以及使用相同底物制备CDNA储存库

摘要

Disclosed is a cloning vector plasmid suitable for preparing cDNA banks. The cloning vector plasmid of the present invention comprises, in the order mentioned from upstream to downstream region unless otherwise specified, a promoter PR1 acting in mammalian cells; an unique restriction enzyme site RE1 rarely existing in eukaryotic DNA and a promoter PR2 of RNA polymerase; an unique restriction enzyme site RE2 generating 3'-protruding dG tail; an unique arbitrary restriction enzyme site RE3; an unique arbitrary restriction enzyme site RE4 generating 3'-protruding terminus; an unique restriction enzyme site RE5 rarely existing in eukaryotic DNA and a promoter PR3 of RNA polymerase; and at least one kind of arbitrary restriction enzyme site RE6 generating 3'-protruding terminus existing at the arbitrary position before the restriction site RE1; and further, at arbitrary positions other than the above-described restriction enzyme sites and promoters, an origin OR1 for replication in mammalian cells, an origin OR2 for replication of a single-stranded phage, an origin OR3 for replication in E. coli, and a selective marker.
机译:公开了适合于制备cDNA库的克隆载体质粒。除非另有说明,否则本发明的克隆载体质粒以从上游到下游区域的顺序包括从上游到下游的顺序,其在哺乳动物细胞中起作用。真核DNA中很少存在的独特限制性酶切位点RE1和RNA聚合酶的启动子PR2;独特的限制性酶切位点RE2,产生3'突出的dG尾巴;独特的任意限制性酶切位点RE3;独特的任意限制性酶切位点RE4,产生3'突出末端;真核DNA中很少存在的独特限制性酶切位点RE5和RNA聚合酶的启动子PR3;在限制性酶切位点RE1之前的任意位置上存在至少一种产生3'突出末端的任意限制性酶切位点RE6。此外,在上述限制酶位点和启动子以外的任意位置,用于在哺乳动物细胞中复制的起点OR1,用于单链噬菌体复制的起点OR2,用于在大肠杆菌中复制的起点OR3,和选择标记。

著录项

  • 公开/公告号JP2994010B2

    专利类型

  • 公开/公告日1999-12-27

    原文格式PDF

  • 申请/专利权人 SAGAMI CHEM RES;

    申请/专利号JP19900238332

  • 发明设计人 KATO MASASHI;AOKI TAKASHI;UMEZAWA YURI;

    申请日1990-09-07

  • 分类号C12N15/09;

  • 国家 JP

  • 入库时间 2022-08-22 01:57:42

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