首页> 外国专利> Method for isolating plasmid DNA from bacterial lysate, involves resuspending bacterial cells in standard buffer, and bacterial cells are lysed with standard buffer e.g. sodium dodecyl sulphate or sodium hydroxide

Method for isolating plasmid DNA from bacterial lysate, involves resuspending bacterial cells in standard buffer, and bacterial cells are lysed with standard buffer e.g. sodium dodecyl sulphate or sodium hydroxide

机译:从细菌裂解物中分离质粒DNA的方法,包括将细菌细胞重悬于标准缓冲液中,并用标准缓冲液如大肠杆菌将细胞裂解。十二烷基硫酸钠或氢氧化钠

摘要

Plasmid DNA isolation involves resuspending bacterial cells in a standard buffer. The bacterial cells are lysed with the standard buffer e.g. sodium dodecyl sulphate (SDS) or sodium hydroxide or by hydrolase e.g. lysozyme which affects the cell wall of bacteria. The lysate is mixed with a binding buffer on the base of a salt-alcohol-mixture with acidic pH-value, so that pH-value, after mixing with lysis buffer, amounts to less than 8. The linked plasmid DNA is washed with a buffer, preferably alcohol containing buffer. The plasmid is extracted by a low salt buffer or water. An independent claim is also included for a kit for isolating plasmid DNA which comprises a standard buffer for resuspending bacterial cell, and a binding buffer on the base of a salt-alcohol-mixture with acidic pH-value.
机译:质粒DNA分离涉及将细菌细胞重悬于标准缓冲液中。细菌细胞用标准缓冲液如十二烷基硫酸钠(SDS)或氢氧化钠或通过水解酶如影响细菌细胞壁的溶菌酶。将裂解物与结合缓冲液在具有酸性pH值的盐-醇混合物的基础上混合,以使与裂解缓冲液混合后的pH值小于8。缓冲液,优选含酒精的缓冲液。用低盐缓冲液或水提取质粒。还包括用于分离质粒DNA的试剂盒的独立权利要求,所述试剂盒包含用于重悬细菌细胞的标准缓冲液,以及在具有酸性pH值的盐-醇混合物的基础上的结合缓冲液。

著录项

  • 公开/公告号DE102007006008A1

    专利类型

  • 公开/公告日2008-08-14

    原文格式PDF

  • 申请/专利权人 AJ INNUSCREEN GMBH;

    申请/专利号DE20071006008

  • 发明设计人

    申请日2007-02-07

  • 分类号C12N15/10;

  • 国家 DE

  • 入库时间 2022-08-21 19:49:26

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