首页> 外国专利> METHOD FOR RAPIDLY TRANSFORMING GRAM-NEGATIVE BACTERIUM AND EXPERIMENT KID FOR PERFORMING THE SAME

METHOD FOR RAPIDLY TRANSFORMING GRAM-NEGATIVE BACTERIUM AND EXPERIMENT KID FOR PERFORMING THE SAME

机译:快速转化革兰氏阴性菌和相同实验动物的方法

摘要

PURPOSE: To provide a method for rapidly transforming a gram-negative bacterium, especially Escherichia coli, and to provide an experimental kid for its performance. ;CONSTITUTION: Escherichia coli is brought into contact with a solution containing a desired plasmid DNA, a polyethylene glycol aqueous solution containing alkali metal ions, and a multiplication medium in this order to perform its phenotypic expression. An Escherichia-receiving container A, a plasmid DNA aqueous solution-receiving container B, a polyethylene glycol aqueous solution-receiving container C, and a multiplication medium-receiving container D are received in a container 1 to form the experimental kid. If necessary, an agar medium for detecting the transformation may be received in the experimental kid. Thereby, the phenotypic expression rapidly proceeds. A freezing temperature operation and a centrifugal operation are not required. The transformation can be carried out even for bacteria not placed in its logarithmic growth period.;COPYRIGHT: (C)1993,JPO&Japio
机译:目的:提供一种快速转化革兰氏阴性细菌,特别是大肠杆菌的方法,并为其性能提供实验依据。组成:将大肠杆菌与含有所需质粒DNA的溶液,含有碱金属离子的聚乙二醇水溶液和繁殖培养基按此顺序进行接触,以进行表型表达。将大肠埃希氏菌容纳容器A,质粒DNA水溶液容纳容器B,聚乙二醇水溶液容纳容器C,以及繁殖介质容纳容器D容纳在容器1中以形成实验小动物。如果有必要,可以在实验儿童中接受用于检测转化的琼脂培养基。因此,表型表达迅速进行。不需要冷冻温度操作和离心操作。甚至对于未处于对数生长期的细菌也可以进行转化。;版权所有:(C)1993,JPO&Japio

著录项

  • 公开/公告号JPH05192169A

    专利类型

  • 公开/公告日1993-08-03

    原文格式PDF

  • 申请/专利权人 SHODA MAKOTO;TECHNO SYST:KK;

    申请/专利号JP19910307808

  • 发明设计人 ANO TAKASHI;SHODA MAKOTO;

    申请日1991-11-22

  • 分类号C12N15/64;B01L11/00;C12N1/21;C12Q1/02;

  • 国家 JP

  • 入库时间 2022-08-22 05:15:55

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