首页> 外国专利> METHOD FOR LOWERING BOTH SEQUENCE VARIATIONS AND INCREASE OF BASE LINES EFFECTS IN DIAGNOSTIC HYBRIDISATION ASSAY, ASSAY FOR PERFORMING SUCH A METHOD AND PROBE FOR USE IN THE ASSAY

METHOD FOR LOWERING BOTH SEQUENCE VARIATIONS AND INCREASE OF BASE LINES EFFECTS IN DIAGNOSTIC HYBRIDISATION ASSAY, ASSAY FOR PERFORMING SUCH A METHOD AND PROBE FOR USE IN THE ASSAY

机译:减少诊断性杂交试验中序列序列变异和增加基线效应的方法,进行该方法的试验和在试验中使用的探针

摘要

The present invention relates to the use in a diagnostic hybridisation assay of a probe or a molecular beacon probe for lowering: the effect of sequence variations in a nucleic acid analyte, and/or the IBL effect due to the possible opening of the stem-loop structure of a molecular beacons by way of (contaminants in the amplification) enzymes, which assay comprises the steps of contacting a set of primers and a sample containing the nucleic acid analyte to amplify the analyte and detecting the amplified analyte or its complement by means of the probe, wherein the probe or molecular beacon probe comprises one or more nucleotides and/or nucleotide analogues that have an affinity increasing modification. The invention also relates to such probe and molecular beacon probe and to a kit for performing a diagnostic assay using such probe or molecular beacon probe.
机译:本发明涉及探针或分子信标探针在诊断杂交测定中的用途,该探针用于降低:核酸分析物中序列变化的影响和/或由于茎环的可能打开而引起的IBL作用通过(扩增中的污染物)酶形成分子信标的结构,该测定包括以下步骤:使一组引物与含有核酸分析物的样品接触以扩增分析物,并通过以下方法检测扩增的分析物或其补体所述探针,其中所述探针或分子信标探针包含具有亲和力增加修饰的一种或多种核苷酸和/或核苷酸类似物。本发明还涉及这样的探针和分子信标探针,以及涉及使用这种探针或分子信标探针进行诊断测定的试剂盒。

著录项

  • 公开/公告号WO2004050911A3

    专利类型

  • 公开/公告日2004-08-19

    原文格式PDF

  • 申请/专利权人 BIOMERIEUX B.V.;VENEMA FOKKE;

    申请/专利号WO2003EP13676

  • 发明设计人 VENEMA FOKKE;

    申请日2003-12-02

  • 分类号C12Q1/68;

  • 国家 WO

  • 入库时间 2022-08-21 22:55:56

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