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Single-molecule DNA amplification and analysis in an integratedmicrofluidic device

机译:集成微流控设备中的单分子DNA扩增和分析

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Stochastic PCR amplification of single DNA template molecules followed by capillary electrophoretic (CE) analysis of the products is demonstrated in an integrated microfluidic device. The microdevice consists of submicroliter PCR chambers etched into a glass substrate that are directly connected to a microfabricated CE system. Valves and hydrophobic vents provide controlled and sensorless loading of the 280-nL PCR chambers; the low volume reactor, the low thermal mass, and the use of thin-film heaters permit cycle times as fast as 30 s, The amplified product, labeled with an intercalating fluorescent dye, is directly injected into the gel-filled capillary channel for electrophoretic analysis. Repetitive PCR analyses at the single DNA template molecule level exhibit quantized product peak areas; a histogram of the normalized peak areas reveals clusters of events caused by 0, 1, 2, and 3 viable template copies in the reactor and these event clusters are shown to fit a Poisson distribution. This device demonstrates the most sensitive PCR possible in a microfabricated device. The detection of single DNA molecules will also facilitate single-cell and single-molecule studies to expose the genetic variation underlying ensemble sequence and expression averages.
机译:在集成的微流控设备中证明了单个DNA模板分子的随机PCR扩增,然后进行了产品的毛细管电泳(CE)分析。微型设备由蚀刻到玻璃基板中的亚微升PCR室组成,该室直接连接到微型CE系统。阀门和疏水阀可对280 nL PCR室进行可控且无传感器的加载。低体积的反应器,低的热质量以及使用薄膜加热器使循环时间缩短至30 s。将带有嵌入荧光染料标记的扩增产物直接注入凝胶填充的毛细管通道中进行电泳分析。在单个DNA模板分子水平上的重复PCR分析显示出定量的产物峰面积;归一化峰面积的直方图显示了反应堆中由0、1、2和3个可行模板副本引起的事件簇,并且这些事件簇显示为符合泊松分布。该设备展示了微型设备中可能最敏感的PCR。单个DNA分子的检测也将有助于单细胞和单分子研究,以揭示整体序列和表达平均值背后的遗传变异。

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