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A nucleic acid strand displacement system for the multiplexed detection of tuberculosis-specific mRNA using quantum dots

机译:核酸链置换系统多路检测tuberculosis-specific信使rna使用量子点

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摘要

The development of rapid, robust and high performance point-of-care diagnostics relies on the advancement and combination of various areas of research. We have developed an assay for the detection of multiple mRNA molecules that combines DNA nanotechnology with fluorescent nanomaterials. The core switching mechanism is toehold-mediated strand displacement. We have used fluorescent quantum dots (QDs) as signal transducers in this assay, as they bring many benefits including bright fluorescence and multiplexing abilities. The resulting assay is capable of multiplexed detection of long RNA targets against a high concentration of background non-target RNA, with high sensitivity and specificity and limits of detection in the nanomolar range using only a standard laboratory plate reader. We demonstrate the utility of our QD-based system for the detection of two genes selected from a microarray-derived tuberculosis-specific gene expression signature. Levels of up-and downregulated gene transcripts comprising this signature can be combined to give a disease risk score, making the signature more amenable for use as a diagnostic marker. Our QD-based approach to detect these transcripts could pave the way for novel diagnostic assays for tuberculosis.
机译:快速的发展,健壮的和高现场即时诊断依赖于性能各领域的进步和组合的研究。检测多个信使rna分子结合DNA纳米技术与荧光纳米材料。toehold-mediated链位移。使用荧光量子点(量子点)信号传感器在这个试验,因为他们带来很多包括明亮的荧光和好处多路复用能力。多路检测长RNA的能力对高浓度的目标背景对非靶标RNA,灵敏度高和特异性的检测和限制摩尔范围只使用一个标准的实验室板的读者。QD-based系统两个基因的检测选择从microarray-derivedtuberculosis-specific基因表达的签名。表达下调基因水平的最新记录由这个签名可以组合一种疾病风险评分,使得签名可以用作一个诊断标记。QD-based方法检测这些记录可以为小说诊断化验吗为肺结核。

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