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Method for simulataneous identification of differentially expresed mRNAS and measurement of relative concentrations

机译:同时鉴定差异表达的miRNA和测定相对浓度的方法

摘要

An improved method for the simultaneous sequence-specific identification of mRNAs in a mRNA population allows the visualization of nearly every mRNA expressed by a tissue as a distinct band on a gel whose intensity corresponds roughly to the concentration of the mRNA. In general, the method comprises the formation of cDNA using anchor primers to fix a 3'-endpoint, producing cloned inserts from the cDNA in a vector containing a bacteriophage-specific promoter for subsequent RNA synthesis, generating linearized fragments of the cloned inserts, preparing cRNA, transcribing cDNA from the cRNA using a set of primers, and performing PCR using a 3'-primer whose sequence is derived from the vector and a set of 5'-primers that is derived from the primers used for transcription of cDNA from cRNA. The method can identify changes in expression of mRNA associated with the administration of drugs or with physiological or pathological conditions.
机译:一种同时对mRNA群体中的mRNA进行序列特异性鉴定的改进方法,可以将组织表达的几乎每个mRNA可视化为凝胶上的一条独特条带,其强度大致对应于mRNA的浓度。通常,该方法包括使用锚定引物固定3'末端形成cDNA,在包含噬菌体特异性启动子的载体中从cDNA产生克隆的插入片段,用于随后的RNA合成,产生克隆的插入片段的线性片段,制备cRNA,使用一组引物从cRNA转录cDNA,并使用3'引物进行PCR,该3'引物的序列源自载体,而5'引物组则源自用于从cRNA转录cDNA的引物。该方法可以鉴定与药物施用或生理或病理状况相关的mRNA表达的变化。

著录项

  • 公开/公告号US5807680A

    专利类型

  • 公开/公告日1998-09-15

    原文格式PDF

  • 申请/专利权人 THE SCRIPPS RESEARCH INSTITUTE;

    申请/专利号US19950544577

  • 发明设计人 J. GREGOR SUTCLIFFE;MARK G. ERLANDER;

    申请日1995-10-17

  • 分类号C12Q1/68;C12P19/34;C07H21/04;

  • 国家 US

  • 入库时间 2022-08-22 02:38:39

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