首页> 外国专利> DETECTION OF MISMATCH IN DOUBLE-STRANDED DNA, DETECTION OF NUCLEIC ACID HAVING MUTATION, AND SEPARATION OF DOUBLE-STRANDED DNA HAVING MISMATCH

DETECTION OF MISMATCH IN DOUBLE-STRANDED DNA, DETECTION OF NUCLEIC ACID HAVING MUTATION, AND SEPARATION OF DOUBLE-STRANDED DNA HAVING MISMATCH

机译:双链DNA错配的检测,核酸突变的检测和双链DNA错配的分离

摘要

PROBLEM TO BE SOLVED: To provide a method for efficiently detecting any mismatch in nucleic acid using MutM protein by contacting subject double-stranded nucleic acid with MutM protein, followed by detecting any binding of the double-stranded nucleic acid to the protein. SOLUTION: This is a method for efficiently detecting any mismatch in double-stranded nucleic acid utilizing MutM protein having an ability of detecting all the mismatches including cytosine in nucleic acid by contacting subject double-stranded nucleic acid which is bound to a support or is labelled so as to be able to bind to a support with MutM protein which is derived from Escherichia coli, and is detectably labelled, binding the double-stranded nucleic acid to MutM protein, followed by detecting any binding of the subject double- stranded nucleic acid to MutM protein. It is also possible to efficiently separate double-stranded nucleic acid containing mismatch(es) from double-stranded nucleic acid containing no mismatch.
机译:解决的问题:提供一种方法,该方法通过使主题双链核酸与MutM蛋白接触,然后检测双链核酸与蛋白质的任何结合,来使用MutM蛋白有效检测核酸中的任何错配。解决方案:这是一种利用MutM蛋白有效检测双链核酸中任何错配的方法,该蛋白具有通过接触与支持物结合或标记的主题双链核酸来检测核酸中包括胞嘧啶在内的所有错配的能力。为了能够与衍生自大肠杆菌并经过可检测标记的MutM蛋白结合至支持物,将双链核酸与MutM蛋白结合,然后检测本主题双链核酸与MutM蛋白。还可以有效地从不包含错配的双链核酸中分离出包含错配的双链核酸。

著录项

  • 公开/公告号JP2000300265A

    专利类型

  • 公开/公告日2000-10-31

    原文格式PDF

  • 申请/专利权人 AMERSHAM PHARMACIA BIOTECH KK;

    申请/专利号JP19990110914

  • 发明设计人 ROBERT F WITTEA;GOTO MASASHIKI;

    申请日1999-04-19

  • 分类号C12N15/09;C07K14/245;C12Q1/68;

  • 国家 JP

  • 入库时间 2022-08-22 02:01:53

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