首页> 外国专利> METHOD FOR EVALUATING GENE EXPRESSION-DEPRESSING EFFECT, AND METHOD FOR DETECTING CLEAVAGE OF mRNA

METHOD FOR EVALUATING GENE EXPRESSION-DEPRESSING EFFECT, AND METHOD FOR DETECTING CLEAVAGE OF mRNA

机译:评价基因表达抑制效果的方法和检测mRNA切割的方法

摘要

PPROBLEM TO BE SOLVED: To provide a method for directly detecting the presence or absence of the cleavage of mRNA or presence or absence of a bond by miRNA. PSOLUTION: This method for evaluating the gene expression-depressing effect is provided by comprising a process of performing a reverse transcription reaction by using a fluorescence-labeled primer and a cell introduced with siRNA or miRNA, or a cell-originated RNA containing an intrinsic miRNA as a template, a process of analyzing by detecting fluorescence generated from a first fluorescence-labeled substance used for the labeling of the fluorescence-labeled primer and measuring the containing ratio (molar ratio) or degree of elongation of an elongated product of the fluorescence-labeled primer in the reverse transcription reaction product, and based on the containing ratio or degree of elongation of obtained elongation product of the fluorescence-labeled primer, a process of evaluating the gene expression-depressing effect by the siRNA, or the like, wherein the hybridizing region with the fluorescence-labeled primer in the mRNA of a target gene is closer to the region of 3' terminal side than the expected cleavage site by the siRNA, or the like, or the expected bonding site by the miRNA. PCOPYRIGHT: (C)2011,JPO&INPIT
机译:

要解决的问题:提供一种直接检测miRNA切割的存在与否或miRNA结合存在或不存在的方法。

解决方案:这种评估基因表达降低效果的方法包括以下步骤:使用荧光标记的引物和导入siRNA或miRNA的细胞或含有以内在miRNA为模板的分析过程,方法是检测从用于标记荧光标记引物的第一荧光标记物质产生的荧光,并测量其延伸产物的含有率(摩尔比)或延伸度逆转录反应产物中的荧光标记引物,以及基于所获得的荧光标记引物的延伸产物的含有比例或延伸程度,通过siRNA评估基因表达抑制效果的过程等。 ,其中靶基因的mRNA中具有荧光标记引物的杂交区域更靠近3'末端区域相对于siRNA等的预期切割位点,或者miRNA的预期结合位点,其l侧。

版权:(C)2011,日本特许厅&INPIT

著录项

  • 公开/公告号JP2011041523A

    专利类型

  • 公开/公告日2011-03-03

    原文格式PDF

  • 申请/专利权人 OLYMPUS CORP;

    申请/专利号JP20090192261

  • 申请日2009-08-21

  • 分类号C12Q1/68;C12N15/09;

  • 国家 JP

  • 入库时间 2022-08-21 18:23:23

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号