组蛋白
组蛋白H3
组蛋白H2A
组蛋白甲基转移酶
表观遗传学
乙酰化
生物
组蛋白甲基化
磷酸化
组蛋白密码
分子生物学
单克隆抗体
EZH2型
组蛋白H1
抗体
细胞生物学
癌症研究
DNA甲基化
基因表达
遗传学
基因
核小体
作者
Tomohiko Yoshimi,Yasuyuki Ohkawa,Masayuki Azuma,Taro Tachibana
标识
DOI:10.1089/mab.2012.0105
摘要
Modification of histone plays a critical role in the epigenetic regulation of gene expression. However, unlike the widely studied roles of histone methylation or acetylation of histone H3, relatively little is known about the molecular mechanisms involved in translating histone phosphorylation into a specific outcome. The present study reports on the development of antibodies (MAbs) directed against phosphorylated histone H3 (S10, T11, S28, S31, and T32), produced by the hybridization of mouse myeloma cells with lymph node cells from an immunized rat or mouse. The MAbs produced specifically recognize different sites of phosphorylation on histone H3. All of these MAbs are suitable for immunoblotting and immunofluorescence analysis. We believe that these antibodies should significantly facilitate our efforts to investigate epigenetic regulation.
科研通智能强力驱动
Strongly Powered by AbleSci AI