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模块化载体六片段金门组装的简便方法。

Easy method for six-fragment Golden Gate Assembly of modular vectors.

作者信息

Cepleanu-Pascu Ionut Adrian, Stan Miruna, Cocioba Sebastian, Stoica Ileana

机构信息

Department of Genetics, Faculty of Biology, University of Bucharest, Bucharest, Romania.

Department of Biochemistry & Molecular Biology, Faculty of Biology, University of Bucharest, Bucharest, Romania.

出版信息

Biotechniques. 2023 Feb;74(2):85-99. doi: 10.2144/btn-2022-0041. Epub 2023 Jan 24.

Abstract

Efficient cloning techniques are a requirement for synthetic biology. This study provides a simplified cloning method based on Golden Gate Assembly that can be used for rapid vector construction. The building of multiple expression vectors with customizable modules is achieved in a timely manner with minimal hands-on time by removing unnecessary steps in the workflow. The authors constructed a total of 21 mammalian episomal expression vectors and conducted a fluorescence expression comparison for different regulatory region combinations post-transfection in HEK293T and HEPG2 cells. Screening revealed that using the EF-1α promoter in combination with the bovine growth hormone polyadenylation sequence seemed to perform best in the types of cells tested compared with other variants.

摘要

高效的克隆技术是合成生物学的一项要求。本研究提供了一种基于金门组装的简化克隆方法,可用于快速构建载体。通过去除工作流程中不必要的步骤,以最少的实际操作时间及时实现了具有可定制模块的多个表达载体的构建。作者总共构建了21个哺乳动物附加型表达载体,并在HEK293T和HEPG2细胞中转染后对不同调控区域组合进行了荧光表达比较。筛选结果显示,与其他变体相比,使用EF-1α启动子与牛生长激素聚腺苷酸化序列组合在测试的细胞类型中表现最佳。

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