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Adaptation of capillary isoelectric focusing to microchannels on a glass chip

机译:毛细管等电聚焦适应玻璃芯片上的微通道

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As a first step toward adaptation of capillary isoelectric focusing (cIEF) to microchannels on a glass chip, we have compared the three most common mobilization methods: chemical, hydrodynamic, and electroosmotic now (EOF)-driven mobilization. Using a commercial cIEF apparatus with coated or uncoated fused-silica capillaries, both chemical and hydrodynamic mobilization gave superior separation efficiency and reproducibility. However, EOF-driven mobilization, which occurs simultaneously with focusing, proved most suitable for miniaturization because of high speed, EOF compatibility and low instrumentation requirements. When this method was tested in a 200-mu m-wide, 10-mu m-deep, and 7-cm-long channel etched into planar glass, a mixture of Cy5-labeled peptides could be focused in less than 30 s, with plate heights of 0.4 mu m (410 plates/s) upon optimization. For a total analysis time of less than 5 min, we estimate a maximum peak capacity of approximately 30-40, interestingly, the order of migration was found to be reversed compared to capillary-based focusing. [References: 25]
机译:作为使毛细管等电聚焦(cIEF)适应玻璃芯片上的微通道的第一步,我们比较了三种最常见的动员方法:化学,流体动力学和电渗现在(EOF)驱动的动员。使用带有涂层或未涂层的熔融石英毛细管的商用cIEF设备,化学和流体动力移动均可提供出色的分离效率和重现性。但是,由于聚焦速度快,EOF兼容且对仪器的要求较低,因此与聚焦同时发生的EOF驱动动员最适合于小型化。当在蚀刻到平板玻璃的200微米宽,10微米深和7厘米长的通道中测试该方法时,可以将Cy5标记的肽混合物聚焦在不到30 s的时间内,优化后的板高为0.4微米(410板/秒)。对于少于5分钟的总分析时间,我们估计最大峰容量约为30-40,有趣的是,与基于毛细管的聚焦相比,发现迁移的顺序是相反的。 [参考:25]

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