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METHOD OF DNA ANALYSIS, DNA ANALYZER, AND PARTS FOR REACTION CHANNEL

机译:DNA分析方法,DNA分析仪和反应通道零件

摘要

PROBLEM TO BE SOLVED: To provide a method of DNA analysis capable of shortening analysis time of a base sequence and simplifying the analysis at a low cost and provide a DNA analyzer.;SOLUTION: This method of DNA analysis is to determine a DNA sequence in one base unit by adding 4 species of deoxynucleotide triphosphate (dNTP: dATP, dCTP, dGTP and dTTP) one by one to a DNA sample and successively detecting the elongation of a primer when the dNTP bonds the DNA sample. Each of the dNTP is marked with a fluorescent dye. Either one of the 4 fluorescent marked dNTP is added one by one to the DNA sample and reacted, with the DNA sample. Subsequently a reagent for decomposing the dNTP is added to the DNA sample to decompose the unreacted fluorescent marked dNTP out of the added fluorescent marked dNTP. After washing the DNA sample, the DNA sample is irradiated with lights. The fluorescent emitted from the fluorescent marked dNTP bonded to the DNA sample is detected to analyze whether the added dNTP bonds the DNA sample and the primer is elongated or not. The DNA analyzer is also provided.;COPYRIGHT: (C)2003,JPO
机译:解决的问题:提供一种能够缩短碱基序列的分析时间并以低成本简化分析的DNA分析方法,并提供一种DNA分析仪。;解决方案:该DNA分析方法是确定DNA序列中的DNA序列。通过将4种脱氧核苷酸三磷酸酯(dNTP:dATP,dCTP,dGTP和dTTP)逐一添加到DNA样品中,并在dNTP与DNA样品结合时连续检测引物的延伸来构建一个碱基单位。每个dNTP均标记有荧光染料。将4种荧光标记的dNTP之一添加到DNA样品中,并与DNA样品反应。随后,将用于分解dNTP的试剂添加到DNA样品中,以从添加的荧光标记的dNTP中分解出未反应的荧光标记的dNTP。洗涤DNA样品后,用光照射DNA样品。检测从与DNA样品结合的标记dNTP的荧光发出的荧光,以分析所添加的dNTP是否与DNA样品结合并且引物是否被拉长。还提供了DNA分析仪。;版权所有:(C)2003,JPO

著录项

  • 公开/公告号JP2003088367A

    专利类型

  • 公开/公告日2003-03-25

    原文格式PDF

  • 申请/专利权人 HITACHI LTD;

    申请/专利号JP20010282887

  • 发明设计人 INAMI HISAO;MIYAKE AKIRA;SASAKI YASUHIKO;

    申请日2001-09-18

  • 分类号C12N15/09;C12M1/00;C12Q1/42;C12Q1/48;C12Q1/68;G01N21/64;G01N33/53;G01N33/58;G01N37/00;

  • 国家 JP

  • 入库时间 2022-08-22 00:14:09

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