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Detection of hybrid double-stranded DNA with antibody after enzyme degradation of excess single-standed DNA

机译:过量单链DNA酶降解后用抗体检测杂交双链DNA

摘要

A method is disclosed for detecting single-stranded target nucleic acid (2) which comprises the steps of forming a hybrid between said target nucleic acid and a nucleic acid probe (4), said nucleic acid probe labelled with an enzyme reagent (6) which hydrolyses single-stranded nucleic acid but is substantially without effect on double-stranded nucleic acid, said hybrid formed under conditions of pH which are outside the activity range of said enzyme reagent, adjusting said pH to a value within the activity range of said enzyme reagent allowing said enzyme reagent substantially to hydrolyse any single-stranded nucleic acid present, and detecting said hybrid.
机译:公开了一种检测单链靶核酸(2)的方法,该方法包括以下步骤:在所述靶核酸和核酸探针(4)之间形成杂交体,所述核酸探针用酶试剂(6)标记,水解单链核酸,但基本上不影响双链核酸,所述杂合体在pH值超出所述酶试剂的活性范围的条件下形成,将所述pH调节至所述酶试剂的活性范围内的值使所述酶试剂基本上水解存在的任何单链核酸,并检测所述杂合体。

著录项

  • 公开/公告号GB2324370B

    专利类型

  • 公开/公告日1999-03-03

    原文格式PDF

  • 申请/专利权人 STUART * HARBRON;

    申请/专利号GB19970007531

  • 发明设计人 STUART * HARBRON;

    申请日1997-04-14

  • 分类号C12Q1/68;

  • 国家 GB

  • 入库时间 2022-08-22 02:10:07

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