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Nanofluidic system for the studies of single DNA molecules.

机译:用于单个DNA分子研究的纳米流体系统。

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摘要

Here, we describe a simple and low-cost lithographic technique to fabricate size-controllable nanopillar arrays inside the microfluidic channels for the studies of single DNA molecules. In this approach, nanosphere lithography has been employed to grow a single layer of well-ordered close-packed colloidal crystals inside the microfluidic channels. The size of the polymeric colloidal nanoparticles could be trimmed by oxygen plasma treatment. These size-trimmed colloidal nanoparticles were then used as the etching mask in a deep etching process. As a result, well-ordered size-controllable nanopillar arrays could be fabricated inside the microfluidic channels. The gap distance between the nanopillars could be tuned between 20 and 80 nm allowing the formation of nanofluidic system where the behavior of a single lambda-phage DNA molecule has been investigated. It was found that the lambda-phage DNA molecule could be fully stretched in the nanofluidic system formed by nanopillars with 50 nm gap distance at afield of 50 V/cm.
机译:在这里,我们描述了一种简单且低成本的光刻技术,可在微流体通道内制造尺寸可控制的纳米柱阵列,用于研究单个DNA分子。在这种方法中,纳米球光刻技术已被用于在微流体通道内生长一层有序的紧密堆积的胶体晶体。聚合物胶体纳米颗粒的尺寸可以通过氧等离子体处理来修整。然后将这些尺寸修整的胶体纳米颗粒用作深蚀刻工艺中的蚀刻掩模。结果,可以在微流体通道内制造有序的尺寸可控的纳米柱阵列。纳米柱之间的间隙距离可以在20至80 nm之间调节,从而形成纳米流体系统,在该系统中已研究了单个λ噬菌体DNA分子的行为。发现λ噬菌体DNA分子可以在由50nm / cm距离的50nm间隙距离的纳米柱形成的纳米流体系统中完全拉伸。

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