首页> 外国专利> MEASURING OF TT VIRUS GENE BY REAL TIME DETECTION PCR METHOD AND PRIMER AND PROBE USED THEREFOR

MEASURING OF TT VIRUS GENE BY REAL TIME DETECTION PCR METHOD AND PRIMER AND PROBE USED THEREFOR

机译:实时检测PCR法,底漆和探针检测TT病毒基因

摘要

PROBLEM TO BE SOLVED: To obtain the subject new primer comprising an oligonucleotide having a sequence of continuous specific base numbers in a specific base sequence and useful for measurement of a new hepatitis virus (TTV) gene, or the like, by real time detecting PCR method.;SOLUTION: A new forward side primer comprising an oligonucleotide having a base sequence (in which T may be U) comprising a continuous 15-39 bases in a base sequence represented by formula I and is used for measurement of TT virus gene by a real time detection PCR method and a new reverse side primer comprising an oligonucleotide having a base sequence (in which T may be U) comprising continuous 15-42 bases in a base sequence represented by formula II, used for measurement of TT virus gene by real time detection PCR method. The forward side and the reverse side primers are obtained by comparing, to design and chemically synthesizing base sequences of various TTV strains registered in database.;COPYRIGHT: (C)2000,JPO
机译:解决的问题:为了获得主题的新引物,该新引物包含具有在特定碱基序列中具有连续的特定碱基数的序列的寡核苷酸,并且可用于通过实时检测PCR来测量新的肝炎病毒(TTV)基因等。解决方案:一种新的正向引物,其包含一种寡核苷酸,该寡核苷酸的碱基序列(其中T可能为U)在式I表示的碱基序列中包含连续的15-39个碱基,用于通过以下方法测量TT病毒基因:实时检测PCR方法和新的反向引物,其包含具有碱基序列(其中T可以是U)的寡核苷酸,该碱基序列在式II表示的碱基序列中包含连续的15-42个碱基,用于通过以下方法测量TT病毒基因:实时检测PCR方法。通过比较,设计和化学合成数据库中注册的各种TTV菌株的碱基序列,获得了正反引物。COPYRIGHT:(C)2000,JPO

著录项

  • 公开/公告号JP2000175700A

    专利类型

  • 公开/公告日2000-06-27

    原文格式PDF

  • 申请/专利权人 SRL INC;

    申请/专利号JP19980360235

  • 发明设计人 KAKINUMA KENICHI;KAWAMATA OSAMU;

    申请日1998-12-18

  • 分类号C12Q1/70;C12N15/09;C12Q1/68;

  • 国家 JP

  • 入库时间 2022-08-22 02:00:37

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