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REAGENT FOR QUANTIATIVE PCR AND QUANTITATIVE PCR METHOD

机译:定量PCR试剂和定量PCR方法

摘要

PROBLEM TO BE SOLVED: To dramatically improve a detective sensibility in a reagent for a quantiative PCR and a quantitative PCR method corresponding to a fluorescent probe method and an intercalator method.SOLUTION: PCR is performed by a reagent 1 for a quantitative PCR including a Taqman (R) probe unit 10 including a Taqman (R) probe 15 with which a metal particle 20, a fluorescent reporter 21, a quencher 22, and a probe 23 are bounded, and configured such that a fluorescent particle and the quencher are separated at the stage where a DNA polymerase reaction is proceeded to a binding region of the Taqman (R) probe 15. The progress of gene amplification is detected by measuring the fluorescent intensity of the fluorescent reporter 21 amplified by a plasmon enhanced field P generated by irradiating the metal particle 20 with excitation light.
机译:解决的问题:显着提高用于定量PCR的试剂的检测灵敏度,以及与荧光探针法和嵌入剂方法相对应的定量PCR方法。解决方案:PCR由试剂1进行,用于包含Taqman的定量PCR (R)探针单元10包括Taqman(R)探针15,金属颗粒20,荧光报告分子21,淬灭剂22和探针23与Taqman(R)探针15结合,并被配置为使得荧光颗粒和淬灭剂在DNA聚合酶反应进行到Taqman(R)探针15的结合区域的阶段。通过测量由通过照射等离子激元增强场P扩增的荧光报告基因21的荧光强度来检测基因扩增的进程。具有激发光的金属颗粒20。

著录项

  • 公开/公告号JP2012147679A

    专利类型

  • 公开/公告日2012-08-09

    原文格式PDF

  • 申请/专利权人 FUJIFILM CORP;

    申请/专利号JP20110006425

  • 发明设计人 HAYASHI KATSUMI;

    申请日2011-01-14

  • 分类号C12Q1/68;G01N21/78;G01N21/64;C12N15/09;

  • 国家 JP

  • 入库时间 2022-08-21 17:43:27

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