首页> 外文会议>2019 20th International Conference on Solid-State Sensors, Actuators and Microsystems amp; Eurosensors XXXIII >Digital Mirna Detection Based on Target Cycling-Induced Fret Signal Amplification
【24h】

Digital Mirna Detection Based on Target Cycling-Induced Fret Signal Amplification

机译:基于目标循环诱发的微动信号放大的数字Mirna检测

获取原文
获取原文并翻译 | 示例

摘要

Absolute quantitative analysis of microRNA (miRNA) plays a vital role in disease diagnosis and cancer studies. Conventional digital miRNA detection methods usually used cDNA obtained from reverse transcription PCR of miRNA as templates, which quantified miRNA indirectly and suffered from low accuracy. This paper reports a novel miRNA detection method based on target cycling-induced FRET signal amplification and droplet microfluidics. It allows, for the first time, direct digital miRNA detection with high selectivity and sensitivity at single-molecule level theoretically. In this method, the full use of miRNA sequence information made the hybridization between targets and DNA probes unique and sensitive, offering high capacity to distinguish single-base mismatches.
机译:microRNA(miRNA)的绝对定量分析在疾病诊断和癌症研究中起着至关重要的作用。常规的数字miRNA检测方法通常以从miRNA的反转录PCR获得的cDNA为模板,从而间接定量miRNA,且准确性较低。本文报道了一种基于靶标循环诱导的FRET信号放大和液滴微流控技术的新型miRNA检测方法。理论上,它首次允许在单分子水平上以高选择性和高灵敏度直接进行数字miRNA直接检测。在这种方法中,充分利用了miRNA序列信息,使靶标与DNA探针之间的杂交变得独特而灵敏,从而提供了区分单碱基错配的高容量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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