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Rapid Prototyping of Microfluidic Systems in Poly(dimethylsiloxane).聚二甲基硅氧烷微流控系统的快速成型
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Hybrid microfluidics: a digital-to-channel interface for in-line sample processing and chemical separations.混合微流控技术:用于在线样品处理和化学分离的数字到通道接口。
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Femtomolar concentration detection limit and zeptomole mass detection limit for protein separation by capillary isoelectric focusing and laser-induced fluorescence detection.毛细管等电聚焦和激光诱导荧光检测的蛋白质分离的飞摩尔浓度检测限和泽摩尔质量检测限。
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Attomole protein analysis by CIEF with LIF detection.通过等速毛细管电泳结合激光诱导荧光检测进行阿托摩尔蛋白质分析。
Electrophoresis. 2009 Jan;30(2):297-302. doi: 10.1002/elps.200800498.
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Generating high peak capacity 2-D maps of complex proteomes using PMMA microchip electrophoresis.使用聚甲基丙烯酸甲酯微芯片电泳生成复杂蛋白质组的高分辨率二维图谱。
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SDS-PAGE of proteins using a chameleon-type of fluorescent prestain.使用变色龙型荧光预染剂对蛋白质进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳。
Anal Chem. 2008 Aug 15;80(16):6274-9. doi: 10.1021/ac800581v. Epub 2008 Jul 11.
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Towards an integrated microfluidic device for spaceflight clinical diagnostics Microchip-based solid-phase extraction of hydroxyl radical markers.迈向用于航天临床诊断的集成微流控装置 基于微芯片的羟基自由基标志物固相萃取
J Chromatogr A. 2008 Jul 25;1200(2):198-203. doi: 10.1016/j.chroma.2008.05.031. Epub 2008 May 22.
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Reaction of fluorogenic reagents with proteins II: capillary electrophoresis and laser-induced fluorescence properties of proteins labeled with Chromeo P465.荧光试剂与蛋白质的反应II:用Chromeo P465标记的蛋白质的毛细管电泳和激光诱导荧光特性
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10
Electrophoresis PDMS/glass chips with continuous on-chip derivatization and analysis of amino acids using naphthalene-2,3-dicarboxaldehyde as fluorogenic agent.采用萘-2,3-二甲醛作为荧光试剂,用于氨基酸连续芯片衍生化和分析的电泳聚二甲基硅氧烷/玻璃芯片。
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聚合物微芯片 CE 可对芯片上或芯片外的变色染料标记的蛋白质进行简化分析。

Polymer microchip CE of proteins either off- or on-chip labeled with chameleon dye for simplified analysis.

机构信息

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, USA.

出版信息

Electrophoresis. 2009 Dec;30(24):4230-6. doi: 10.1002/elps.200900349.

DOI:10.1002/elps.200900349
PMID:19924700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2805013/
Abstract

Microchip CE of proteins labeled either off- or on-chip with the "chameleon" CE dye 503 using poly(methyl methacrylate) microchips is presented. A simple dynamic coating using the cationic surfactant CTAB prevented nonspecific adsorption of protein and dye to the channel walls. The labeling reactions for both off- and on-chip labeling proceeded at room temperature without requiring heating steps. In off-chip labeling, a 9 ng/mL concentration detection limit for BSA, corresponding to a approximately 7 fg (100 zmol) mass detection limit, was obtained. In on-chip tagging, the free dye and protein were placed in different reservoirs of the microchip, and an extra incubation step was not needed. A 1 microg/mL concentration detection limit for BSA, corresponding to a approximately 700 fg (10 amol) mass detection limit, was obtained from this protocol. The earlier elution time of the BSA peak in on-chip labeling resulted from fewer total labels on each protein molecule. Our on-chip labeling method is an important part of automation in miniaturized devices.

摘要

本文介绍了一种使用聚甲基丙烯酸甲酯微芯片,对在芯片上或在芯片外标记的蛋白质进行微芯片毛细管电泳(CE)的方法。通过使用阳离子表面活性剂 CTAB 进行简单的动态涂层处理,可以防止蛋白质和染料非特异性地吸附到通道壁上。无论是在芯片外还是在芯片内进行标记,标记反应都可以在室温下进行,无需加热步骤。在芯片外标记中,获得了对 BSA 的 9ng/mL 浓度检测限,相当于大约 7fg(100zmol)的质量检测限。在芯片内标记中,将游离染料和蛋白质分别放置在微芯片的不同储液器中,无需额外的孵育步骤。从该方案中获得了对 BSA 的 1μg/mL 浓度检测限,相当于大约 700fg(10amol)的质量检测限。在芯片内标记中,BSA 峰的洗脱时间较早,这是因为每个蛋白质分子上的总标记数量较少。我们的芯片内标记方法是小型化设备自动化的重要组成部分。