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一种基于短毛细管的高速 DNA 片段分离的自动化毛细管电泳系统。

An automated capillary electrophoresis system for high-speed separation of DNA fragments based on a short capillary.

机构信息

Institute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, PR China.

出版信息

Electrophoresis. 2010 Oct;31(19):3184-91. doi: 10.1002/elps.201000362.

DOI:10.1002/elps.201000362
PMID:22216429
Abstract

A high-speed DNA fragment separation system was developed based on a short capillary and a slotted-vial array automated sample introduction system. The injection process of DNA sample in a short capillary was investigated systematically with three injection techniques including constant-field-strength, low-field-strength and translational spontaneous injections. Under the optimized conditions, picoliter-scale sample plugs (corresponding to ca. 20-μm plug length) were obtained, which ensure the high-speed and high-efficiency separation for DNA fragments with a short effective separation length. Other separation conditions including the sieving matrix concentration, separation field strength and effective separation length were also optimized. The present system was applied in the separation of ΦX174-Hae III digest DNA marker. With an effective separation length of 2.5 cm, the separation could be achieved in <100 s with plate heights ranging from 0.21 to 0.74 μm (corresponding to plate numbers from 4.86 × 10(6) to 1.36 × 10(6)/m). The repeatabilities for the migration time of the eleven fragments were between 0.4 and 1.1% RSD (n=8). By using the automated continuous injection method, the separation for four different DNA samples could be achieved within 250 s. The present system was further applied in the fast sizing of real DNA samples of PCR products.

摘要

基于短毛细管和槽式管阵列自动进样系统,开发了一种高速 DNA 片段分离系统。系统研究了短毛细管中 DNA 样品的三种进样技术,包括恒场强、低场强和平移自发进样。在优化条件下,获得了皮升级别的样品塞(约 20-μm 塞长),确保了短有效分离长度的 DNA 片段的高速高效分离。还优化了其他分离条件,包括筛分基质浓度、分离场强和有效分离长度。本系统应用于 ΦX174-Hae III 消化 DNA 标记物的分离。在 2.5cm 的有效分离长度下,<100s 即可完成分离,理论塔板高度在 0.21-0.74μm 之间(对应 4.86×10(6)到 1.36×10(6)/m 的理论塔板数)。十一个片段的迁移时间的重复性在 0.4-1.1%RSD 之间(n=8)。通过使用自动连续进样方法,可在 250s 内完成四个不同 DNA 样品的分离。该系统还进一步应用于 PCR 产物的实际 DNA 样品的快速尺寸测定。

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