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使用梯度洗脱等速电泳从粗提样品中提取人源 DNA 用于身份鉴定。

DNA purification from crude samples for human identification using gradient elution isotachophoresis.

机构信息

Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA.

出版信息

Electrophoresis. 2013 Sep;34(17):2522-30. doi: 10.1002/elps.201300133.

Abstract

Gradient elution isotachophoresis (GEITP) was demonstrated for DNA purification, concentration, and quantification from crude samples, represented here by soiled buccal swabs, with minimal sample preparation prior to human identification using STR analysis. During GEITP, an electric field applied across leading and trailing electrolyte solutions resulted in isotachophoretic focusing of DNA at the interface between these solutions, while a pressure-driven counterflow controlled the movement of the interface from the sample reservoir into a microfluidic capillary. This counterflow also prevented particulates from fouling or clogging the capillary and reduced or eliminated contamination of the delivered DNA by PCR inhibitors. On-line DNA quantification using laser-induced fluorescence compared favorably with quantitative PCR measurements and potentially eliminates the need for quantitative PCR prior to STR analysis. GEITP promises to address the need for a rapid and robust method to deliver DNA from crude samples to aid the forensic community in human identification.

摘要

梯度洗脱等速电泳(GEITP)可用于从原始样品(如污染的口腔拭子)中纯化、浓缩和定量 DNA,在进行 STR 分析进行人类鉴定之前,只需进行最少的样品制备。在 GEITP 中,在先导和尾随电解液之间施加电场会导致 DNA 在这些溶液之间的界面处进行等速电泳聚焦,而压力驱动的逆流则控制界面从样品库移动到微流控毛细管中。这种逆流还可以防止颗粒堵塞或堵塞毛细管,并减少或消除 PCR 抑制剂对输送 DNA 的污染。使用激光诱导荧光进行在线 DNA 定量与定量 PCR 测量结果相当,并且可能消除在 STR 分析之前进行定量 PCR 的需要。GEITP 有望满足从原始样品中快速可靠地输送 DNA 的需求,以帮助法医界进行人类识别。

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