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A method for analysis of biological materials based on gel electrophoresis using barcode DNA

机译:基于条形码的凝胶电泳分析生物材料的方法

摘要

Magnetic fine particles bound with a first ligand that specifically binds to a target analyte; And a method for analyzing gel electrophoresis-based biomaterials using nanoparticles comprising a second ligand that specifically binds to a target analyte and at least one barcode DNA. The present invention relates to a method for detecting and analyzing a trace amount of biomolecules without amplification processes such as PCR using nanoparticles containing a large number of barcode DNAs and gel electrophoresis generally used or for detecting sensitive signals . The detection method according to the present invention is capable of detecting miRNAs that are difficult to detect because they are difficult to detect and can detect even minute amounts of atomol concentration (aM; 10 -18 M) or 1 젭 mole level and can identify single-base-inconsistent sequences And quantitatively analyzing a plurality of components from multiple complex samples at one time by using barcode DNAs of various sizes. Therefore, the method can be usefully used for diagnosis of cancer and detection of mutation from clinical samples.
机译:与第一配体结合的磁性微粒,该第一配体与目标分析物特异性结合;以及一种使用纳米颗粒分析基于凝胶电泳的生物材料的方法,所述纳米颗粒包含与目标分析物和至少一个条形码DNA特异性结合的第二配体。 [0001]本发明涉及一种无需扩增过程即可检测和分析痕量生物分子的方法,所述扩增过程不使用诸如通常使用的含有大量条形码DNA的纳米颗粒的PCR或凝胶电泳或用于检测敏感信号的PCR。根据本发明的检测方法能够检测难以检测的miRNA,因为它们难以检测,并且甚至可以检测微量的原子浓度(aM; 10 -18 M)或1。 젭摩尔水平,可识别单碱基不一致的序列,并使用各种大小的条形码DNA一次定量分析多个复杂样品中的多种成分。因此,该方法可用于诊断癌症和检测临床样品中的突变。

著录项

  • 公开/公告号KR101537165B1

    专利类型

  • 公开/公告日2015-07-15

    原文格式PDF

  • 申请/专利权人 서울대학교산학협력단;

    申请/专利号KR20130130567

  • 发明设计人 남좌민;이효진;박정은;

    申请日2013-10-30

  • 分类号C12Q1/68;C12N15/11;G01N33/53;

  • 国家 KR

  • 入库时间 2022-08-21 14:57:56

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