首页> 外国专利> Carry-Over Protection in Enzyme-Based Dna Amplification Systems Targeting Methylation Analysis

Carry-Over Protection in Enzyme-Based Dna Amplification Systems Targeting Methylation Analysis

机译:针对甲基化分析的基于酶的Dna扩增系统中的残留保护

摘要

The invention refers to a method for providing a decontaminated template nucleic acid for enzymatic amplification reactions suitable for DNA methylation analysis. This method is characterized by the following steps: a) incubating a nucleic acid with a chemical reagent or an enzyme-containing solution, whereby the unmethylated cytosine bases are converted into uracil bases, b) mixing the template nucleic acid from step a) with the components required for an enzyme-mediated amplification reaction, including at least two oligonucleotides, whereby at least one of said oligonucleotides comprises i) at least one sequence part that hybridizes with a sequence of the template nucleic acid to be amplified, and ii) at least one sequence part that constitutes a recognition site for a DNA cleaving enzyme that cleaves DNA downstream of said recognition site and c) adding to this mixture a DNA cleaving enzyme, which specifically binds to the at least one sequence part that is a recognition site, and d) incubating the mixture, whereby nucleic acids containing said recognition site for a DNA cleaving enzyme are degraded.
机译:本发明涉及一种用于提供适于DNA甲基化分析的酶促扩增反应的去污染的模板核酸的方法。该方法的特征在于以下步骤:a)用化学试剂或含酶溶液孵育核酸,从而将未甲基化的胞嘧啶碱基转化为尿嘧啶碱基,b)将步骤a)的模板核酸与酶介导的扩增反应所需的组分,包括至少两个寡核苷酸,其中至少一个所述寡核苷酸包含i)与待扩增模板核酸序列杂交的至少一个序列部分,和ii)至少一个序列部分,其构成用于切割所述识别位点下游的DNA的DNA切割酶的识别位点,和c)向该混合物中加入特异性结合至少一个作为识别位点的序列部分的DNA切割酶,和d)温育混合物,从而降解包含所述DNA切割酶的识别位点的核酸。

著录项

  • 公开/公告号US2011027834A1

    专利类型

  • 公开/公告日2011-02-03

    原文格式PDF

  • 申请/专利权人 REIMO TETZNER;DIMO DIETRICH;

    申请/专利号US20070308149

  • 发明设计人 REIMO TETZNER;DIMO DIETRICH;

    申请日2007-06-08

  • 分类号C12P19/34;C12N9/00;C07H21/04;

  • 国家 US

  • 入库时间 2022-08-21 18:11:48

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