| 货号 | 12244S |
| 描述 | This Cell Signaling Technology antibody is conjugated to Alexa Fluor® 647 fluorescent dye and tested in-house for direct flow cytometric and immunofluorescent analysis in human cells. The antibody is expected to exhibit the same species cross-reactivity as the unconjugated Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb #9728. |
| 反应种属 | Human/Mouse/Rat/Monkey |
| 来源宿主 | Rabbit |
| 应用 | IF-IC/F |
| 目标/特异性 | Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb (Alexa Fluor® 647 Conjugate) recognizes endogenous levels of histone H3 when di-methylated at Lys27. The antibody shows some cross-reactivity with mono-methylated Lys27, but does not cross-react with non-methylated or tri-methylated Lys27. In addition, the antibody does not cross-react with mono-methylated, di-methylated or tri-methylated histone H3 Lys4, Lys9, Lys36, or histone H4 Lys20. |
| 使用方法 | F(1:50) IF-IC (1:50) |
| 供应商 | CST |
| 标记 | Alexa Fluor 647 |
| 背景 | The nucleosome, made up of four core histone proteins (H2A, H2B, H3, and H4), is the primary building block of chromatin. Originally thought to function as a static scaffold for DNA packaging, histones have now been shown to be dynamic proteins, undergoing multiple types of post-translational modifications, including acetylation, phosphorylation, methylation, and ubiquitination (1). Histone methylation is a major determinant for the formation of active and inactive regions of the genome and is crucial for the proper programming of the genome during development (2,3). Arginine methylation of histones H3 (Arg2, 17, 26) and H4 (Arg3) promotes transcriptional activation and is mediated by a family of protein arginine methyltransferases (PRMTs), including the co-activators PRMT1 and CARM1 (PRMT4) (4). In contrast, a more diverse set of histone lysine methyltransferases has been identified, all but one of which contain a conserved catalytic SET domain originally identified in the Drosophila Su(var)3-9, Enhancer of zeste, and Trithorax proteins. Lysine methylation occurs primarily on histones H3 (Lys4, 9, 27, 36, 79) and H4 (Lys20) and has been implicated in both transcriptional activation and silencing (4). Methylation of these lysine residues coordinates the recruitment of chromatin modifying enzymes containing methyl-lysine binding modules such as chromodomains (HP1, PRC1), PHD fingers (BPTF, ING2), tudor domains (53BP1), and WD-40 domains (WDR5) (5-8). The discovery of histone demethylases such as PADI4, LSD1, JMJD1, JMJD2, and JHDM1 has shown that methylation is a reversible epigenetic marker (9). |
| 存放说明 | 4C |
Flow cytometric analysis of Jurkat cells using Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb (Alexa Fluor® 647 Conjugate) (blue) compared to concentration-matched Rabbit (DA1E) mAb IgG XP® Isotype Control (Alexa Fluor® 647 Conjugate) #2985 (red).流式细胞术检测Jurkat细胞活性，使用的抗体为Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb (Alexa Fluor® 647 Conjugate)（蓝色）与使用浓度匹配的Rabbit (DA1E) mAb IgG XP® Isotype Control (Alexa Fluor® 647 Conjugate) #2985的相比较（红色）。 | |
Confocal immunofluorescent analysis of HeLa cells using Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb (Alexa Fluor® 647 Conjugate) (red). Actin filaments were labeled with Alexa Fluor® 488 Phalloidin #8878 (green).采用共聚焦免疫荧光术检测HeLa细胞，使用的抗体为Di-Methyl-Histone H3 (Lys27) (D18C8) XP® Rabbit mAb (Alexa Fluor® 647 Conjugate) (红色)。肌动蛋白微丝使用Alexa Fluor® 488 Phalloidin #8878进行标记（绿色）。 |
