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High-density small-volume gel loading directly from capillary tubes

机译:高密度小体积凝胶直接从毛细管上样

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摘要

A technique has been developed for high lane density loading of small-volume DNA samples in a horizontal agarose gel. This technique has been investigated with a simple hand-held tool that is made to couple to sample output from a new capillary-based sample automation system. The approach consists of piercing the gel with pressurized sample capillaries and relieving the pressure shortly before withdrawal. The pressurization prevents the capillary from aspirating the gel buffer and keeps the sample at the tip of the capillary, so that it may be sucked into the gel during withdrawal. This method is shown to be adequate for a wide range of DNA ladders and PCR-based screening. In addition to allowing smaller lanes and a higher lane density than is achievable with traditional well-forming techniques, it relaxes the need for well formation and the alignment of the sample loader with those wells, providing an easy, efficient means of loading agarose gels.
机译:已经开发出一种用于在水平琼脂糖凝胶中高通量密度装载小体积DNA样品的技术。该技术已通过简单的手持工具进行了研究,该工具可与新的基于毛细管的样品自动化系统的样品输出耦合。该方法包括用加压的样品毛细管刺穿凝胶,并在撤回前不久释放压力。加压可防止毛细管吸取凝胶缓冲液,并将样品保持在毛细管的尖端,以便在抽出过程中将其吸入凝胶中。事实证明,该方法适用于各种DNA阶梯和基于PCR的筛选。除了允许比传统的成孔技术更小的泳道和更高的泳道密度外,它还放宽了对孔的形成以及样品装载器与这些孔对齐的需求,从而提供了一种简单,有效的琼脂糖凝胶装载方法。

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