货号 | 4176S |
反应种属 | Human |
来源宿主 | Rabbit |
应用 | W/IP/IF-F/IF-IC |
使用方法 | WB(1:1000) IP (1:200) IF-F (1:100) IF-IC (1:100) |
供应商 | CST |
背景 | β-Catenin is a key downstream effector in the Wnt signaling pathway (1). It is implicated in two major biological processes in vertebrates: early embryonic development (2) and tumorigenesis (3). CK1 phosphorylates β-catenin at Ser45. This phosphorylation event primes β-catenin for subsequent phosphorylation by GSK-3β (4-6). GSK-3β destabilizes β-catenin by phosphorylating it at Ser33, Ser37, and Thr41 (7). Mutations at these sites result in the stabilization of β-catenin protein levels and have been found in many tumor cell lines (8). |
存放说明 | -20C |
计算分子量 | 92 |
Confocal immunofluorescent analysis of HeLa cells, untreated (left), λ phosphatase-treated (middle), or untreated NCI-H28 cells (β-catenin null; right) using Phospho-β-Catenin (Ser675) (D2F1) XP® Rabbit mAb (green). Actin filaments have been labeled with DY-554 phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye). 对未处理(左)或λ-磷酸酶处理(中)的HeLa细胞,或未经处理的NCI-H28细胞(β-catenin 缺失;右)使用Phospho-β-Catenin (Ser675) (D2F1) XP® Rabbit mAb (绿色)进行激光共聚焦荧光分析。肌动蛋白丝使用DY-554phalloidin(红色)标记.蓝色伪彩=DRAQ5® #4084 (DNA荧光染料). | |
Western blot analysis of extracts from MKN-45 and SK-N-MC cells, untreated or treated with λ phosphatase for 1 hour or forskolin (FSK) for 30 minutes, using Phospho-β-Catenin (Ser675) (D2F1) XP® Rabbit mAb (upper) or β-Catenin (6B3) Rabbit mAb #9582 (lower). MKN-45 and SK-N-MC 细胞,未处理或经λ磷酸酶处理1小时或用福斯科林(FSK)处理30分钟,获得细胞提取物,使用Phospho-β-Catenin (Ser675) (D2F1) XP® Rabbit mAb(上) 或β-Catenin (6B3) Rabbit mAb #9582 (下)进行western blot分析。 | |
Confocal immunofluorescent analysis of rat colon using Phospho-β-Catenin (Ser675) (D2F1) XP® Rabbit mAb (green). Actin filaments have been labeled with DY-554 Phalloidin (red). Blue pseudocolor = DRAQ5® #4084 (fluorescent DNA dye). 使用Phospho-β-Catenin (Ser675) (D2F1) XP® Rabbit mAb (绿色)对大鼠结肠组织进行激光共聚焦荧光分析. 肌动蛋白丝使用DY-554 Phalloidin(红色)标记。蓝色伪彩=DRAQ5® #4084 (DNA荧光染料). |