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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Highly sensitive and multiple DNA biosensor based on isothermal strand-displacement polymerase reaction and functionalized magnetic microparticles
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Highly sensitive and multiple DNA biosensor based on isothermal strand-displacement polymerase reaction and functionalized magnetic microparticles

机译:基于等温链置换聚合酶反应和功能化磁性微粒的高灵敏多DNA生物传感器

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摘要

A universal, highly sensitive and selective chemiluminescence (CL) imaging method has been developed for high throughput detection of DNA. After molecular beacon (MB) hybridized with the target DNA, the biotin-labeled primer was attached to a magnetic microparticle (MMP) surface by hybridization with the stem part of the MB to initiate a polymerization of DNA strand, which led to the release of the target and another polymerization cycle. Thus the polymerization produced the multiplication of biotin-labeled primer on the surface of MMPs. Sequentially, the horseradish peroxidase (HRP) was conjugated to MMPs surface through the biotin-streptavidin reaction. Then, the conjugated HRP was determined by the CL imaging method. This proposed method could detect the sequence-specific DNA as low as 0.4 pM and discriminate perfectly matched target DNA from the mismatch DNAs. All in all, this proposed method exhibited an efficient amplification performance, and would open new opportunities for sensitive and high throughput detection of DNA.
机译:已经开发出一种通用的,高度灵敏且选择性的化学发光(CL)成像方法,用于DNA的高通量检测。分子信标(MB)与目标DNA杂交后,生物素标记的引物通过与MB的茎部杂交而附着于磁性微粒(MMP)表面,从而引发DNA链聚合,从而导致DNA链的释放目标和另一个聚合周期。因此,聚合在MMP的表面上产生了生物素标记的引物的繁殖。依次,辣根过氧化物酶(HRP)通过生物素-链霉亲和素反应与MMPs结合。然后,通过CL成像方法确定缀合的HRP。该方法可检测低至0.4 pM的序列特异性DNA,并从错配DNA中区分出完全匹配的靶DNA。总而言之,该提出的方法表现出有效的扩增性能,并且将为DNA的灵敏和高通量检测打开新的机会。

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