货号 | 9764S |
反应种属 | Human/Mouse/Rat |
来源宿主 | Rabbit |
应用 | W/IP/IF-IC/F |
目标/特异性 | Phospho-Histone H3 (Thr11) Antibody detects endogenous levels of histone H3 only when phosphorylated at threonine 11. The antibody does not cross-react with other phosphorylated histones or with acetylated histones. |
使用方法 | WB(1:1000) IP (1:50) F (1:25) IF-IC (1:100) |
供应商 | CST |
背景 | Modulation of chromatin structure plays an important role in the regulation of transcription in eukaryotes. The nucleosome, made up of DNA wound around eight core histone proteins (two each of H2A, H2B, H3, and H4), is the primary building block of chromatin (1). The amino-terminal tails of core histones undergo various post-translational modifications, including acetylation, phosphorylation, methylation, and ubiquitination (2-5). These modifications occur in response to various stimuli and have a direct effect on the accessibility of chromatin to transcription factors and, therefore, gene expression (6). In most species, histone H2B is primarily acetylated at Lys5, 12, 15, and 20 (4,7). Histone H3 is primarily acetylated at Lys9, 14, 18, 23, 27, and 56. Acetylation of H3 at Lys9 appears to have a dominant role in histone deposition and chromatin assembly in some organisms (2,3). Phosphorylation at Ser10, Ser28, and Thr11 of histone H3 is tightly correlated with chromosome condensation during both mitosis and meiosis (8-10). Phosphorylation at Thr3 of histone H3 is highly conserved among many species and is catalyzed by the kinase haspin. Immunostaining with phospho-specific antibodies in mammalian cells reveals mitotic phosphorylation at Thr3 of H3 in prophase and its dephosphorylation during anaphase (11). |
存放说明 | -20C |
计算分子量 | 17 |
Western blot analysis of lysates from HeLa, C6 and NIH/3T3 cells treated for 24 hours with or without nocodazole and also with or without λ phosphatase, using Phospho-Histone H3 (Thr11) Antibody #9764 (upper) or Histone H3 Antibody #9715 (lower). 使用Phospho-Histone H3 (Thr11) Antibody #9764 (upper) or Histone H3 Antibody #9715 (lower),免疫印迹(Western blot)分析HeLa、C6和NIH/3T3裂解物,这些细胞未使用或使用nocodazole处理24小时,并且使用和未使用λ phosphatase。 | |
Flow cytometric analysis of untreated Jurkat cells, using Phospho-Histone H3 (Thr11) Antibody versus propidium iodide (DNA content). The boxed population indicates Phospho-Histone H3 (Thr11)-positive cells. | |
使用Phospho-Histone H3 (Thr11) Antibody和propidium iodide (DNA含量),流式细胞仪分析未处理的Jurkat细胞。方框代表Phospho-Histone H3 (Thr11)阳性细胞。 |