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植物原生质体的分离、培养及瞬时转化

Isolation, culture, and transient transformation of plant protoplasts.

作者信息

Shen Jinbo, Fu Jiaxin, Ma Jin, Wang Xiangfeng, Gao Caiji, Zhuang ChuXiong, Wan Jianmin, Jiang Liwen

机构信息

School of Life Sciences, Centre for Cell and Developmental Biology and State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Hong Kong, China.

出版信息

Curr Protoc Cell Biol. 2014 Jun 3;63:2.8.1-17. doi: 10.1002/0471143030.cb0208s63.

Abstract

Transient gene expression in protoplasts, which has been used in several plant species, is an important and versatile tool for rapid functional gene analysis, protein subcellular localization, and biochemical manipulations. This unit describes transient gene expression by electroporation of DNA into protoplasts of Arabidopsis or tobacco suspension-cultured cells and by polyethylene glycol (PEG)-mediated DNA transformation into protoplasts derived from rice leaf sheaths. PEG-mediated DNA transformation for transient gene expression in rice protoplasts in suspension culture is also described as an alternative technique. Methods for collecting intracellular and secreted proteins are also provided.

摘要

原生质体中的瞬时基因表达已在多种植物物种中得到应用,是一种用于快速功能基因分析、蛋白质亚细胞定位和生化操作的重要且通用的工具。本单元介绍了通过电穿孔将DNA导入拟南芥或烟草悬浮培养细胞的原生质体以及通过聚乙二醇(PEG)介导的DNA转化导入水稻叶鞘来源的原生质体来进行瞬时基因表达。还介绍了在悬浮培养的水稻原生质体中进行瞬时基因表达的PEG介导的DNA转化作为替代技术。此外,还提供了收集细胞内和分泌蛋白的方法。

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