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Distance and Microsphere Aggregation-Based DNA Detection in a Paper-Based Microfluidic Device

机译:基于纸微流体装置的距离和微球聚集基DNA检测

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摘要

In paper-based microfluidics, the simplest devices are colorimetric, giving qualitative results. However, getting quantitative data can be quite a bit more difficult. Distance-based devices provide a user-friendly means of obtaining quantitative data without the need for any additional equipment, simply by using an included ruler or calibrated markings. This article details the development of a quantitative DNA detection device that utilizes the aggregation of polystyrene microspheres to affect the distance that microspheres wick through filter paper. The microspheres are conjugated to single-stranded DNA (ssDNA) oligomers that are partially complementary to a target strand and, in the presence of the target strand, form a three-strand complex, resulting in the formation of aggregates. The higher the concentration of the target strand, the larger the aggregate, and the shorter the distance wicked by the microspheres. This behavior was investigated across a wide range of target concentrations and under different incubation times to understand aggregate formation. The device was then used to successfully detect a target strand spiked in extracted plant DNA.
机译:在基于纸质的微流体中,最简单的设备是比色,提供定性结果。但是,获得量化数据可能更加困难。基于距离的器件提供了一种用户友好的方法,可以通过使用包括的尺寸或校准标记来获得无需任何附加设备的定量数据。本文详细介绍了使用聚苯乙烯微球的聚集的定量DNA检测装置的开发,以影响微球芯通过滤纸的距离。微球与单链DNA(SSDNA)低聚物缀合,所述单链DNA(SSDNA)低聚物与靶链部分互补,并且在靶链的存在下,形成三股复合物,导致聚集体的形成。靶链的浓度越高,聚集体越大,微球的距离越短。在各种目标浓度和不同的孵化时间下调查这种行为以了解聚集体形成。然后将该装置用于成功检测在提取的植物DNA中尖刺的靶链。

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