首页> 外国专利> ULTRA-RAPID AND SENSITIVE DNA DETECTION USING DNAZYME AND ON-CHIP ISOTACHOPHORESIS

ULTRA-RAPID AND SENSITIVE DNA DETECTION USING DNAZYME AND ON-CHIP ISOTACHOPHORESIS

机译:脱氧核糖核酸酶和芯片上同位素电泳技术进行超灵敏的DNA检测

摘要

A DNA detection method combines DNAzyme reactions and on-chip isotachophoresis (ITP). A mixture of sample containing a target DNA and a DNAzyme sensor which is either (1) a catalytic molecular beacon or (2) a binary DNAzyme and a probe is loaded into a trailing electrolyte (TE) reservoir of a microfluidic chip. In the presence of the target DNA, the catalytic molecular beacon or the probe is cleaved to generate a fluorescent fragment. Enhanced DNAzyme reaction occurs at the TE-to-LE interface. Fluorescent signal from cleaved catalytic molecular beacon or probe is detected either at the location where DNAzyme reaction occurs or at a separate location. In the latter case, the microfluidic chip has a separation region containing a capture gel or a sieving matrix which allows the fluorescent fragment to pass through but captures or traps the uncleaved catalytic molecular beacon or probe.
机译:DNA检测方法结合了DNAzyme反应和片上等速电泳(ITP)。将包含目标DNA和(1)催化分子信标或(2)二元DNAzyme和探针的DNAzyme传感器的样品混合物装入微流控芯片的尾随电解质(TE)容器中。在靶DNA的存在下,催化分子信标或探针被裂解以产生荧光片段。增强的DNA酶反应发生在TE到LE的界面。来自裂解的催化分子信标或探针的荧光信号在DNAzyme反应发生的位置或在单独的位置检测。在后一种情况下,微流体芯片具有包含捕获凝胶或筛分基质的分离区域,该分离区域允许荧光片段通过但捕获或捕获未裂解的催化分子信标或探针。

著录项

  • 公开/公告号US2015197791A1

    专利类型

  • 公开/公告日2015-07-16

    原文格式PDF

  • 申请/专利权人 KONICA MINOLTA LABORATORY U.S.A. INC.;

    申请/专利号US201514590482

  • 发明设计人 NORIAKI YAMAMOTO;

    申请日2015-01-06

  • 分类号C12Q1/68;

  • 国家 US

  • 入库时间 2022-08-21 15:26:24

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