货号 | 9683S |
描述 | This Cell Signaling Technology antibody is conjugated to Alexa Fluor® 488 fluorescent dye and tested in-house for direct flow cytometry and immunofluorescent analysis in human cells. The antibody is expected to exhibit the same species cross-reactivity as the unconjugated Acetyl-Histone H3 (Lys9) (C5B11) Rabbit mAb #9649. |
反应种属 | Human/Mouse/Rat/Monkey/Zebrafish/C.elegans |
来源宿主 | Rabbit |
应用 | IF-IC/F |
目标/特异性 | Acetyl-Histone H3 (Lys9) (C5B11) Rabbit mAb (Alexa Fluor® 488 Conjugate) detects endogenous levels of histone H3 only when acetylated on Lys9. This antibody does not cross-react with other acetylated histones. |
使用方法 | F(1:50) IF-IC (1:400) |
供应商 | CST |
标记 | Alexa Fluor 488 |
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 | 4C |
Flow cytometric analysis of HeLa cells, untreated (blue) or SAHA-treated (green), using Acetyl-Histone H3 (Lys9) (C5B11) Rabbit mAb (Alexa Fluor® 488 Conjugate). 使用Acetyl-Histone H3 (Lys9) (C5B11) Rabbit mAb兔单抗 (Alexa Fluor® 488 Conjugate),流式细胞仪分析未处理的HeLa细胞,细胞分为untreated (蓝色)或SAHA-treated (绿色)。 | |
Confocal immunofluorescent analysis of HeLa cells, treated with TSA #9950 (left) and untreated (right), using Acetyl-Histone H3 (Lys9) (C5B11) Rabbit mAb (Alexa Fluor® 488 Conjugate) (green). Actin filaments have been labeled with DY-554 phalloidin (red). 使用Acetyl-Histone H3 (Lys9) (C5B11) Rabbit mAb 兔单抗(Alexa Fluor® 488 Conjugate)(绿色),共聚焦免疫荧光分析HeLa细胞,细胞分为TSA #9950 treated (左图)和untreated (#9950;右图)。DY-554 phalloidin标记微丝蛋白(红色)。 |