染色质免疫沉淀
芯片对芯片
芯片排序
组蛋白
染色质
组蛋白密码
嘉雅宠物
生物
表观遗传学
表观遗传学
计算生物学
染色质重塑
细胞生物学
遗传学
DNA
基因表达
基因
DNA甲基化
发起人
核小体
作者
Thomas A. Milne,Keji Zhao,Jay L. Hess
标识
DOI:10.1007/978-1-59745-418-6_21
摘要
Disruption of epigenetic regulators of transcription is a central mechanism of oncogenesis. Many of the advances in the understanding of these mechanisms are attributable to the successful development of chromatin immunoprecipitation (ChIP) for in vivo detection of histone modifications as well as chromatin binding regulatory proteins. This is a powerful technique for analyzing histone modifications as well as binding sites for proteins that bind either directly or indirectly to DNA. Here we present two ChIP protocols. The first is particularly useful for identifying histone modifications or binding at specific, known genomic sites. The second, employing serial analysis of gene expression, is particularly powerful for the discovery of previously unidentified sites of modification or binding.
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