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

NEW MATERIAL:The title plasmid positioning a restriction enzyme site RE1 from promoter PR1 for mammalian cells toward downstream, promoter PR2 of RNA polymerase, restriction enzyme site RE2, restriction enzyme site RE3, restriction enzyme site RE4, restriction enzyme site RE5 and RNA polymerase promoter PR3, positioning restriction enzyme site RE6 at an arbitrary place of the restriction enzyme site RE1, replication origin OR1 for mammalian cells, replication origin OR2 of single strand phage, replication origin OR3 for Escherichia coil and a selecting marker at an arbitrary position. EXAMPLE:Vector pKA1. USE:Preparation of cDNA bank. PREPARATION:Plasmid pTZ18RP4 obtained from plasmid pTZ18R and plasmid pKAO obtained from plasmid pTZ19U are subjected to a process shown by the formula to give cloning vector pKA1 of example.
机译:新材料:标题质粒位于哺乳动物细胞启动子PR1下游的限制性内切酶位点RE1,RNA聚合酶的启动子PR2,限制性内切酶位点RE2,限制性内切酶位点RE3,限制性内切酶位点RE4,限制性内切酶位点RE5和RNA聚合酶启动子PR3,将限制性酶切位点RE6定位在限制性酶切位点RE1的任意位置,哺乳动物细胞的复制起点OR1,单链噬菌体的复制起点OR2,大肠杆菌的复制起点OR3和选择标记在任意位置。示例:向量pKA1。用途:制备cDNA库。制备:将从质粒pTZ18R获得的质粒pTZ18RP4和从质粒pTZ19U获得的质粒pKAO进行下式所示的过程,以得到实施例的克隆载体pKA1。

著录项

  • 公开/公告号JPH04117292A

    专利类型

  • 公开/公告日1992-04-17

    原文格式PDF

  • 申请/专利权人 SAGAMI CHEM RES CENTER;

    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C12N15/00;C07K14/525;C12N15/09;C12N15/10;C12N15/70;C12N15/85;

  • 国家 JP

  • 入库时间 2022-08-22 05:42:57

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号