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Direct translational analysis of electrophoretically separated DNA using a cell-free protein synthesis system

机译:使用无细胞蛋白质合成系统直接平移分析电泳分离的DNA

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摘要

Cell-based protein production has low throughput and restricted flexibility in process design. For the development of a rapid platform for translational analysis of genetic sequences by bypassing time- and labor-consuming steps of cell-based gene expression methods, we attempted in this study to combine the techniques of gel electrophoresis and cell-free protein synthesis in a streamlined manner. After an electrophoretic separation of the DNAs of varying sizes, DNAs in the gel matrices were directly incubated in a reaction mixture for cell-free protein synthesis, which led to successful expression of functional proteins. (C) 2016 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
机译:基于细胞的蛋白质产生具有低通量和限制过程设计的灵活性。 通过绕过基于细胞基因表达方法的时间和劳动阶段的时间和劳动阶段的遗传序列的快速平台的发展,我们在该研究中尝试结合凝胶电泳和无细胞蛋白质合成的技术 简化的方式。 在不同尺寸的DNA的电泳分离之后,将凝胶基质中的DNA直接孵育在反应混合物中以进行无细胞蛋白质合成,这导致了功能性蛋白的成功表达。 (c)2016年韩国工程和工程化学学会。 elsevier b.v出版。保留所有权利。

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