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通过流式细胞术监测启动子活性

Monitoring Promoter Activity by Flow Cytometry.

作者信息

Taher Taher E I

机构信息

Experimental Medicine and Rheumatology, William Harvey Research Institute, Charterhouse Square, London, EC1M 6BQ, UK.

出版信息

Methods Mol Biol. 2017;1651:65-73. doi: 10.1007/978-1-4939-7223-4_6.

Abstract

Genetic reporters have become invaluable tools for indirectly monitoring promoter activities. The quantitative measurement of promoter activities using reporter gene systems is fundamental for pharmaceutical, biomedical, and molecular biology research. Genetic reporters are used not only for measuring promoter activities but also for understanding the mechanisms controlling gene transcription and in the identification, and characterization of cis-acting regulatory elements. Fluorescent reporter proteins including enhanced green fluorescent protein (EGFP ) are reliable for monitoring quantitative underlying differences in promoter activities. The emitted fluorescence intensity of the expressed reporter is measured at the single-cell level by flow cytometry and represents a readout for the promoter activities. In this chapter, the protocol for measurement and analyzing of transfected cells expressing the reporter gene EGFP is thoroughly described and fully illustrated.

摘要

遗传报告基因已成为间接监测启动子活性的重要工具。使用报告基因系统对启动子活性进行定量测量是药物、生物医学和分子生物学研究的基础。遗传报告基因不仅用于测量启动子活性,还用于理解控制基因转录的机制以及顺式作用调控元件的鉴定和表征。包括增强型绿色荧光蛋白(EGFP)在内的荧光报告蛋白对于监测启动子活性的定量潜在差异是可靠的。通过流式细胞术在单细胞水平测量表达的报告基因发出的荧光强度,它代表了启动子活性的读数。在本章中,将全面描述并充分说明测量和分析表达报告基因EGFP的转染细胞的方案。

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