首页> 外国专利> SYNTHETIC INTRON DNA, RECOMINANT DNA CONTAINING THE SAME AND TRANSFORMANT TRANSFORMED THEREWITH

SYNTHETIC INTRON DNA, RECOMINANT DNA CONTAINING THE SAME AND TRANSFORMANT TRANSFORMED THEREWITH

机译:合成的内含子DNA,包含相同的重组DNA,并在其中进行了转化

摘要

NEW MATERIAL:A synthetic intron DNA, having a region containing the 5' and 3'-terminal consesus sequences and a region containing a sequence of a branching part, either of at least one set of recurring base sequences in the opposite directions being a sequence of region containing a consesus sequence and/or a region containing the branching part and at least one of the above- mentioned one set of the base sequences in the opposite directions, present in base sequences other than the above-mentioned regions and sandwiching regions containing the sequence of the branching part. USE:A genetic expression controlling agent and reagent for elucidating a splicing mechanism. PREPARATION:For example, a synthetic intron is linked to a plasmid pUC118 and cloned to provided a plasmid pUC-INTRON, which is then cleaved with restriction enzymes SnaBI and PstI to afford DNA fragments. The resultant DNA fragments are then linked to a DNA fragment cleaved with restriction enzymes XbaI and PstI using a T4DNA ligase to provided a synthetic intron DNA.
机译:新材料:一种合成内含子DNA,具有一个包含5'和3'末端共有序列的区域和一个包含分支部分序列的区域,其中至少一组在相反方向上的重复碱基序列中的任一个是一个序列包含共有序列的区域和/或包含分支部分的区域和在相反方向上存在的上述一组碱基序列中的至少一个的序列,存在于除上述区域和包含分支部分的顺序。用途:用于阐明剪接机理的基因表达控制剂和试剂。制备:例如,将合成内含子与质粒pUC118连接并克隆以提供质粒pUC-INTRON,然后将其用限制酶SnaBI和PstI裂解以提供DNA片段。然后使用T4DNA连接酶将所得的DNA片段与用限制性酶XbaI和PstI切割的DNA片段连接,以提供合成的内含子DNA。

著录项

  • 公开/公告号JPH02142482A

    专利类型

  • 公开/公告日1990-05-31

    原文格式PDF

  • 申请/专利权人 WAKUNAGA PHARMACEUT CO LTD;

    申请/专利号JP19880296960

  • 发明设计人 NAKAWA FUMIKIYO;YOSHIMATSU TADANORI;

    申请日1988-11-24

  • 分类号C12N15/09;C12N1/19;C12N15/79;C12N15/81;C12R1/865;

  • 国家 JP

  • 入库时间 2022-08-22 06:24:57

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