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Detection method based on signal-amplified DNA cascade reaction with target extension

机译:基于带有靶标延伸的信号放大的DNA级联反应的检测方法

摘要

Methods, compositions and kits for detecting a target nucleic acid in a sample. The method comprises a first signal DNA generating sequence, an endonuclease recognition site, and a sequence complementary to the 3 ′ end of the target nucleic acid in the 5 ′ to 3 ′ direction in the presence of a polymerase and an endonuclease. A second oligonucleotide comprising, in 5 ′ to 3 ′ direction, a second signal DNA generating sequence, an endonuclease recognition site, and a sequence homologous to the first signal DNA generating sequence of the first oligonucleotide In a 5 ′ to 3 ′ direction, a third oligonucleotide and sample comprising a sequence homologous to the third signal DNA generating sequence, the endonuclease recognition site, and the second signal DNA generating sequence of the second oligonucleotide. Including contacting. The reaction causes a signal cascade. The polymerase preferably has strand displacement activity, and the target nucleic acid is preferably microRNA.
机译:用于检测样品中靶核酸的方法,组合物和试剂盒。该方法包括第一信号DNA产生序列,核酸内切酶识别位点和在聚合酶和核酸内切酶存在下与靶核酸的5'至3'方向的3'末端互补的序列。第二寡核苷酸,其在5'至3'方向上包括第二信号DNA产生序列,核酸内切酶识别位点和与第一寡核苷酸的第一信号DNA产生序列同源的序列,在5'至3'方向上,第三寡核苷酸和样品,其包含与第二寡核苷酸的第三信号DNA产生序列,核酸内切酶识别位点和第二信号DNA产生序列同源的序列。包括联系。该反应导致信号级联。聚合酶优选具有链置换活性,并且靶核酸优选是微小RNA。

著录项

  • 公开/公告号JP2018504898A

    专利类型

  • 公开/公告日2018-02-22

    原文格式PDF

  • 申请/专利权人 アボット・ラボラトリーズ;

    申请/专利号JP20170534193

  • 发明设计人 小森 誠;吉村 徹;

    申请日2015-12-24

  • 分类号C12Q1/68;C12N15/09;C12N9/12;C12N9/16;

  • 国家 JP

  • 入库时间 2022-08-21 13:09:12

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