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Exploiting biased reptation for continuous flow preparative DNA fractionation in a versatile microfluidic platform

机译:在多功能微流控平台中利用偏倚重复进行连续流制备性DNA分离

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摘要

A new approach is presented for preparative, continuous flow fractionation of sub-10-kbp DNA fragments, which exploits the variation in the field-dependent mobility of the DNA molecules based on their length. Orthogonally pulsed electric fields of significantly different magnitudes are applied to a microchip filled with a sieving matrix of 1.2% agarose gel. Using this method, we demonstrate a high-resolution separation of 0.5, 1, 2, 5, and 10 kbp DNA fragments within 2 min. During the separation, DNA fragments are also purified from other ionic species. Preparative fractionation of sub-10-kbp DNA molecules plays an important role in second-generation sequencing. The presented device performs rapid high-resolution fractionation and it can be reliably manufactured with simple microfabrication procedures.
机译:提出了一种新的方法,用于亚10 kbp DNA片段的制备性,连续流分级分离,该方法利用了DNA分子基于长度的场依赖性迁移率的变化。将具有明显不同幅度的正交脉冲电场施加到装有1.2%琼脂糖凝胶筛分基质的微芯片上。使用这种方法,我们证明了在2分钟内可以高分辨率分离0.5、1、2、5和10kbp DNA片段。在分离过程中,DNA片段也从其他离子物种中纯化出来。 10 kbp以下的DNA分子的制备级分在第二代测序中起着重要作用。所提出的装置执行快速的高分辨率分级分离,并且可以通过简单的微细加工程序可靠地制造。

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