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A dual amplification strategy for ultrasensitive detection of microRNA

机译:microRNA超灵敏检测的双重扩增策略

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摘要

Here, we present a dual amplification strategy based on a duplex-specific nuclease and a hybridization chain reaction, which has been designed for the highly sensitive detection of miRNAs. In the first step, a loop amplification strategy based on a duplex-specific nuclease was employed to obtain a large number of ssDNA reporters that then act as initiators to trigger the next amplification step. The second step involves a hybridization chain reaction based on two hairpin DNAs denoted as H-1 and H-2. Doxorubicin-CdTe quantum dots, which function as detecting indicators that intercalated into the hybridization chain reaction products, lead to significantly amplified electrochemiluminescence signal readout. This dual amplification strategy enabled the sensitive detection of let-7d from 10 aM to 10 nM with a detection limit of 10 aM, and offered an excellent capacity to discriminate between microRNA family members. This assay therefore offers great potential applications in biomedical research and early clinical diagnosis. (C) 2017 Elsevier B.V. All rights reserved.
机译:在这里,我们提出了一种基于双链特异性核酸酶和杂交链反应的双重扩增策略,该策略设计用于miRNA的高灵敏度检测。在第一步中,采用基于双链特异性核酸酶的环扩增策略来获得大量的ssDNA报告分子,然后将其用作引发剂来触发下一扩增步骤。第二步涉及基于两个发夹DNA(称为H-1和H-2)的杂交链反应。阿霉素-CdTe量子点起插入杂交链反应产物的检测指示剂的作用,导致显着放大的电化学发光信号读数。这种双重扩增策略使灵敏的let-7d检测范围从10 aM到10 nM,检测极限为10 aM,并提供了出色的区分微小RNA家族成员的能力。因此,该测定法在生物医学研究和早期临床诊断中提供了巨大的潜在应用。 (C)2017 Elsevier B.V.保留所有权利。

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