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Methods for detection of ataxia telangiectasia mutations

机译:共济失调毛细血管扩张突变的检测方法

摘要

The present invention is directed to a method of screening large, complex, polyexonic eukaryotic genes such as the ATM gene for mutations and polymorphisms by an improved version of single strand conformation polymorphism (SSCP) electrophoresis that allows electrophoresis of two or three amplified segments in a single lane. The present invention also is directed to new mutations and polymorphisms in the ATM gene that are useful in performing more accurate screening of human DNA samples for mutations and in distinguishing mutations from polymorphisms, thereby improving the efficiency of automated screening methods.
机译:本发明涉及一种通过改进的单链构象多态性(SSCP)电泳方法筛选大的,复杂的,多异源的真核基因(例如ATM基因)的突变和多态性的方法,该方法允许对一个或两个扩增片段进行电泳。单行道。本发明还针对ATM基因中的新突变和多态性,其可用于对人类DNA样品进行更准确的突变筛选,以及将突变与多态性区别开,从而提高自动化筛选方法的效率。

著录项

  • 公开/公告号US6951724B2

    专利类型

  • 公开/公告日2005-10-04

    原文格式PDF

  • 申请/专利权人 RICHARD A. GATTI;

    申请/专利号US20020175225

  • 发明设计人 RICHARD A. GATTI;

    申请日2002-06-17

  • 分类号C12Q1/68;C12P19/34;C07H21/04;

  • 国家 US

  • 入库时间 2022-08-21 22:19:46

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