首页> 美国卫生研究院文献>Biosensors >Microfluidic-Based Amplification-Free Bacterial DNA Detection by Dielectrophoretic Concentration and Fluorescent Resonance Energy Transfer Assisted in Situ Hybridization (FRET-ISH) †‡
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Microfluidic-Based Amplification-Free Bacterial DNA Detection by Dielectrophoretic Concentration and Fluorescent Resonance Energy Transfer Assisted in Situ Hybridization (FRET-ISH) †‡

机译:通过介电泳浓度和荧光共振能量转移辅助原位杂交(FRET-ISH)的基于微流体的无扩增细菌DNA检测†‡

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摘要

Although real-time PCR (RT-PCR) has become a diagnostic standard for rapid identification of bacterial species, typical methods remain time-intensive due to sample preparation and amplification cycle times. The assay described in this work incorporates on-chip dielectrophoretic capture and concentration of bacterial cells, thermal lysis, cell permeabilization, and nucleic acid denaturation and fluorescence resonance energy transfer assisted in situ hybridization (FRET-ISH) species identification. Combining these techniques leverages the benefits of all of them, allowing identification to be accomplished completely on chip less than thirty minutes after receipt of sample, compared to multiple hours required by traditional RT-PCR and its requisite sample preparation.
机译:尽管实时PCR(RT-PCR)已成为快速鉴定细菌种类的诊断标准,但是由于样品制备和扩增循环时间长,典型的方法仍然耗时。这项工作中描述的测定法包括芯片上的双电泳捕获和细菌细胞的浓缩,热裂解,细胞通透性以及核酸变性和荧光共振能量转移辅助的原位杂交(FRET-ISH)物种鉴定。结合使用这些技术可充分利用所有技术的优势,与传统RT-PCR及其必需的样品制备所需的多个小时相比,允许在接收样品后不到30分钟的时间内完全在芯片上完成鉴定。

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