首页> 外国专利> A RAPID DNA EXTRACTION METHOD FOR PCR-BASED ANALYSIS OF TRANSGENIC FISH

A RAPID DNA EXTRACTION METHOD FOR PCR-BASED ANALYSIS OF TRANSGENIC FISH

机译:基于PCR的转基因鱼快速DNA提取方法

摘要

The present invention relates to a method for quickly the transgenic fish and extract of good quality DNA that can be used in PCR to organizations of trace from small transgenic fish to economic analysis, dodecyl tissue collected from fish room sodium sulfate; DNA comprising the step of culturing in a basic buffered solution containing (sodium dodecyl sulfate SDS) and neutralized by addition of a buffer solution containing a non-ionic surface active agent in the culture medium and recovering the supernatant after centrifuging them According to the extraction method, it is possible to quickly secure a small amount of template DNA that can be used for PCR from fish fin 20 minutes, and so at the same time provides a good template for PCR DNA with no difference at all and the purified DNA, which is required by the prior art DNA complex separation process, expensive removal of the protein enzyme and the reaction time can not be required over the time Well, the time required for the release of transgenic fish prior analysis, we can significantly reduce the costs and efforts.
机译:本发明涉及一种用于快速转基因鱼和高质量DNA提取物的方法,该方法可用于PCR以从小型转基因鱼到经济分析,从鱼室硫酸钠中收集的十二烷基组织的痕量组织。 DNA包括以下步骤:在含有(十二烷基硫酸钠SDS)的碱性缓冲溶液中培养,并通过在培养基中添加含有非离子表面活性剂的缓冲溶液进行中和,并在离心分离后根据回收方法回收上清液。 ,可以快速确保从鱼鳍中提取20分钟可用于PCR的少量模板DNA,因此同时提供了一个好的PCR DNA模板,与纯化的DNA完全没有区别。现有技术所需的DNA复合物的分离过程中,不需要昂贵的去除蛋白质酶和反应时间,因此,经过事先分析释放转基因鱼所需要的时间,我们可以大大降低成本和工作量。

著录项

  • 公开/公告号KR100470803B1

    专利类型

  • 公开/公告日2005-03-10

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20020058029

  • 申请日2002-09-25

  • 分类号C12N15/10;

  • 国家 KR

  • 入库时间 2022-08-21 22:04:11

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