发起人
染色质免疫沉淀
电泳迁移率测定
DNA结合蛋白
抄写(语言学)
DNA
分子生物学
一般转录因子
生物
基因表达
细胞生物学
遗传学
转录因子
基因
语言学
哲学
作者
Ryan R. Chaparian,Julia C. van Kessel
出处
期刊:Methods in molecular biology
日期:2020-01-01
卷期号:: 165-172
被引量:17
标识
DOI:10.1007/7651_2020_307
摘要
Transcription factors are ubiquitous proteins that associate with promoter DNA and regulate gene expression through a variety of mechanisms. Understanding transcriptional control mechanisms requires in-depth investigation of the binding of transcription factors to the promoters they regulate. There are many in vivo and in vitro methods for testing the binding of a known protein to a promoter, such as chromatin immunoprecipitation and electrophoretic mobility shift assays. However, for these experiments, one must have a protein candidate to test and is not able to identify unknown proteins bound to a particular promoter. Thus, the promoter pull-down assay was developed to fill this void. This method uses DNA as bait to capture proteins that bind to a specific promoter, such as transcription factors, from cellular lysates. Coupled with other experiments, the promoter pull-down assay vastly improves the repertoire of methods available for defining regulatory complexes that influence transcription.
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