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Electrophoretic separation of antisense dna using polymer-solution filled capillary by cross-injection

机译:用聚合物溶液填充毛细血管通过交叉注射电泳分离反义DNA

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Different lengths of antisense DNA are nromally separated by polyacrylamide gel-filled column using capillary electrophoresis. The rigid gel bed, however, has a limited lifetime due to the forming of air bubbles and clogging particularly when a real sample with complex matrix is analyzed. An alternative is to replace the gel with a replenishable polymer solution. In this work, a capillary electrophoresis system using a microcross (10nL) connected with four 75 mum i.d. fused-silica capillaries and operated under high-voltage shunting is described to implement the PEG sieving medium for the separation of antisense DNAs. Both the separation and injection capillaries were filled with polyethylene glycol (PEG) in tris-borate buffer and the separation was performed with pinched-mode. The PEG medium was found to resolve the 15-20mers of antisense DNA under a conventional linear configuration. Substantial band broadening, however, was observed when using the cross configuration udner the same separation conditions. A better control of the injection time as well as the applied voltage is required to minimize the sample diffusion.
机译:使用毛细管电泳,通过聚丙烯酰胺凝胶柱柱的不同长度的反义DNA。然而,由于在分析了具有复杂基质的真实样品时,刚性凝胶床具有有限的寿命。替代方案是用可补充的聚合物溶液替换凝胶。在这项工作中,使用微区(10nl)的毛细管电泳系统与四个75 mum i.d.描述了熔融二氧化硅毛细管和在高压分流下操作,以实现用于分离反义DNA的PEG筛分介质。分离和注射毛细血管在三硼酸酯缓冲液中填充聚乙二醇(PEG),并用挤压模式进行分离。发现PEG培养基以在常规的线性构型下解析15-20mer的反义DNA。然而,当使用相同的分离条件时,观察到当使用交叉配置UDNER时观察到大量带宽。需要更好地控制喷射时间以及施加的电压来最小化样品扩散。

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