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Sensitive and inexpensive digital DNA analysis by microfluidic enrichment of rolling circle amplified single-molecules

机译:通过微流体富集滚动圆的敏感和廉价的数字DNA分析扩增单分子

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摘要

Single molecule quantification assays provide the ultimate sensitivity and precision for molecular analysis. However, most digital analysis techniques, i.e. droplet PCR, require sophisticated and expensive instrumentation for molecule compartmentalization, amplification and analysis. Rolling circle amplification (RCA) provides a simpler means for digital analysis. Nevertheless, the sensitivity of RCA assays has until now been limited by inefficient detection methods. We have developed a simple microfluidic strategy for enrichment of RCA products into a single field of view of a low magnification fluorescent sensor, enabling ultra-sensitive digital quantification of nucleic acids over a dynamic range from 1.2 aM to 190 fM. We prove the broad applicability of our analysis platform by demonstrating 5-plex detection of as little as similar to 1 pg (similar to 300 genome copies) of pathogenic DNA with simultaneous antibiotic resistance marker detection, and the analysis of rare oncogene mutations. Our method is simpler, more cost-effective and faster than other digital analysis techniques and provides the means to implement digital analysis in any laboratory equipped with a standard fluorescent microscope.
机译:单分子定量测定提供了用于分子分析的最终敏感性和精度。然而,大多数数字分析技术,即液滴PCR,需要复杂和昂贵的分子舱化,扩增和分析仪器。滚动圆放大(RCA)提供了一种用于数字分析的更简单方法。然而,RCA测定的敏感性直到现在受到低效检测方法的限制。我们开发了一种简单的微流体策略,将RCA产品富集到低放大荧光传感器的单个视野中,从1.2A至190 fm的动态范围内实现超敏感的核酸数字量化。我们通过证明5-POX检测与具有同时抗生素抗性标志物检测的致病性DNA的1pg(类似于300个基因组拷贝)和罕见的癌基因突变分析,证明了我们分析平台的广泛适用性。我们的方法比其他数字分析技术更简单,更具成本效益,更快,并提供了在配备标准荧光显微镜的任何实验室中实现数字分析的手段。

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