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Microchip-based purification of DNA from biological samples

机译:基于微芯片的生物样品DNA纯化

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A microchip solid-phase extraction method for purification of DNA from biological samples, such as blood, is demonstrated. Silica beads were packed into glass microchips and the beads immobilized with sol-gel to provide a stable and reproducible solid phase onto which DNA could be adsorbed. Optimization of the DNA loading conditions established a higher DNA recovery at pH 6.1 than 7.6. This lower pH also allowed for the flow rate to be increased, resulting in a decrease in extraction time from 25 min to less than 15 min. Using this procedure, template genomic DNA from human whole blood was purified on the microchip platform with the only sample preparation being mixing of the blood with load buffer prior to loading on the microchip device. Comparison between the microchip SPE (muchipSPE) procedure and a commercial microcentrifuge method showed comparable amounts of PCR-amplifiable DNA could be isolated from cultures of Salmonella typhimurium. The greatest potential of the muchipSPE device was illustrated by purifying DNA from spores from the vaccine strain of Bacillus anthracis, where eventual integration of SPE, PCR, and separation on a single microdevice could potentially enable complete detection of the infectious agent in less than 30 min. [References: 30]
机译:演示了一种微芯片固相提取方法,可从血液等生物样品中纯化DNA。将二氧化硅珠粒包装到玻璃微芯片中,并用溶胶-凝胶固定化珠粒,以提供可吸附DNA的稳定且可复制的固相。 DNA上样条件的优化确定了pH 6.1高于7.6的DNA回收率。较低的pH值还可以提高流速,从而使提取时间从25分钟减少到不到15分钟。使用此程序,在微芯片平台上纯化了来自人类全血的模板基因组DNA,唯一的样品前处理是将血液与加载缓冲液混合,然后再加载到微芯片设备上。微芯片SPE(muchipSPE)程序与商业微离心方法之间的比较表明,可以从鼠伤寒沙门氏菌培养物中分离出相当数量的PCR扩增DNA。通过从炭疽芽孢杆菌疫苗菌株的孢子中纯化DNA来说明muchipSPE设备的最大潜力,最终将SPE,PCR和在单个微型设备上的分离整合在一起,有可能在不到30分钟的时间内完全检测出传染原。 。 [参考:30]

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