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在亚微升微流控超声处理装置中 DNA 的碎片化。

Fragmentation of DNA in a sub-microliter microfluidic sonication device.

机构信息

Genome Biology Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, Heidelberg, 69117, Germany.

出版信息

Lab Chip. 2012 Nov 21;12(22):4677-82. doi: 10.1039/c2lc40595d.

Abstract

Fragmentation of DNA is an essential step for many biological applications including the preparation of next-generation sequencing (NGS) libraries. As sequencing technologies push the limits towards single cell and single molecule resolution, it is of great interest to reduce the scale of this upstream fragmentation step. Here we describe a miniaturized DNA shearing device capable of processing sub-microliter samples based on acoustic shearing within a microfluidic chip. A strong acoustic field was generated by a Langevin-type piezo transducer and coupled into the microfluidic channel via the flexural lamb wave mode. Purified genomic DNA, as well as covalently cross-linked chromatin were sheared into various fragment sizes ranging from ∼180 bp to 4 kb. With the use of standard PDMS soft lithography, our approach should facilitate the integration of additional microfluidic modules and ultimately allow miniaturized NGS workflows.

摘要

DNA 碎片化是许多生物学应用的必要步骤,包括下一代测序 (NGS) 文库的制备。随着测序技术朝着单细胞和单分子分辨率的方向发展,减少这种上游碎片化步骤的规模具有重要意义。在这里,我们描述了一种基于微流控芯片内声剪切的微型 DNA 剪切设备,能够处理亚微升样品。强声场由兰格文型压电换能器产生,并通过弯曲型兰姆波模式耦合到微流道中。纯化的基因组 DNA 以及共价交联的染色质被剪切为各种大小的片段,从 ∼180 bp 到 4 kb 不等。通过使用标准的 PDMS 软光刻技术,我们的方法应该有助于集成其他微流控模块,并最终实现小型化的 NGS 工作流程。

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