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High lane density slab gel electrophoresis by micromachined instrumentation

机译:微机械仪表高通道密度板坯凝胶电泳

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One of the challenges of future miniaturized biochemical analysis laboratories is to manipulate sub-μL samples in parallel fashion. Since the development and implementation of the 96-well microtiter plate technology, considerable progress hasbeen made to increase the plate density. A number of high-density formats have been developed based on the well-established 96-well format, including 386, 864, and 1536 wells. The available sample handling systems, however, are lagging due to widecenter-to-center spacing (~4.5 mm) and inability to handle sample volumes below 0.5μL. Also, these systems are capable of dispensing only 6 to 12 pipettes at one time. With the current trends of miniaturizing biochemical analysis techniques and thedrive toward the development of a Micro Total Analysis System (μTAS), techniques must be developed to allow macroscale spatial manipulation of sub-μL sample volumes in a highly parallel manner at sub-mm spacing. In this work, we present an approach formacroscopic manipulation of pL to μL fluid volumes [1] and demonstrate the application to slab gel electrophoresis.
机译:未来小型化生化分析实验室的挑战之一是以并行方式操纵亚μl样品。自96孔微量滴定板技术的开发和实施以来,对板密度增加了相当大的进展。已经基于已建立的96孔格式开发了许多高密度格式,包括386,864和1536孔。然而,由于扩散到中心间距(〜4.5mm),可用的样品处理系统滞后是滞后(〜4.5mm),无法处理0.5μl以下的样品体积。此外,这些系统能够一次仅分配6到12个移液器。随着小型化的生化分析技术和thedrive朝向微全分析系统(μTAS)的发展的当前趋势,技术必须被开发以允许子μL样品体积的宏观尺度空间操纵在亚毫米间隔的高度并行的方式进行。在这项工作中,我们向μl流体体积[1]呈现PL的方法是骨髓镜的操纵,并证明施加到平板凝胶电泳。

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