货号 | 3440S |
反应种属 | Human/Monkey |
来源宿主 | Mouse |
应用 | W/IHC-P/IF-IC |
使用方法 | WB(1:1000) IHC-P (1:3200) IF-IC (1:200) |
供应商 | CST |
背景 | Chk2 is the mammalian orthologue of the budding yeast Rad53 and fission yeast Cds1 checkpoint kinases (1-3). The amino-terminal domain of Chk2 contains a series of seven serine or threonine residues (Ser19, Thr26, Ser28, Ser33, Ser35, Ser50 and Thr68) each followed by glutamine (SQ or TQ motif). These are known to be preferred sites for phosphorylation by ATM/ATR kinases (4,5). After DNA damage by ionizing radiation (IR), UV irradiation or hydroxyurea treatment, Thr68 and other sites in this region become phosphorylated by ATM/ATR (5-7). The SQ/TQ cluster domain, therefore, seems to have a regulatory function. Phosphorylation at Thr68 is a prerequisite for the subsequent activation step, which is attributable to autophosphorylation of Chk2 on residues Thr383 and Thr387 in the activation loop of the kinase domain (8).Chk2是哺乳动物中和芽殖酵母Rad53和裂殖酵母Cds1检验点激酶同源的蛋白(1-3)。Chk2的氨基末端结构域包含有一个七丝氨酸或者苏氨酸残基(Ser19, Thr26, Ser28, Ser33, Ser35, Ser50 and Thr68)组成的系列,每个系列紧跟着谷氨酸(SQ 或TQ模体)。这些地方是已知的ATM/ATR激酶磷酸化的首选作用位点(4,5)。电离辐射(IR)引起DNA损伤之后,UV照射处理或者羟基脲处理,这个区域的68位苏氨酸和其他位点被ATM/ATR磷酸化(5-7)。因此,SQ/TQ簇结构域似乎具有调节功能。第68位苏氨酸的磷酸化是后续激活步骤的先决条件,激活归因于激酶结构域激活回路中Chk2第383位和387位苏氨酸残基的自体磷酸化(8)。 |
存放说明 | -20C |
计算分子量 | 62 |
Western blot analysis of extracts from various cell types using Chk2 (1C12) Mouse mAb.Western blot方法检测不同细胞提取物,使用的抗体为Chk2 (1C12) Mouse mAb。 | |
Confocal immunofluorescent analysis of HeLa cells using Chk2 (1C12) Mouse mAb (green). Actin filaments have been labeled with DY-554 phalloidin (red).激光共聚焦方法检测HeLa细胞,使用的抗体为Chk2 (1C12) Mouse mAb ,呈绿色。肌动蛋白纤维用DY-554鬼笔环肽标记,呈红色。 | |
Immunohistochemical analysis of paraffin-embedded human breast carcinoma using Chk2 (1C12) Mouse mAb.免疫组织化学方法检测石蜡包埋人类乳腺癌组织,使用的抗体为Chk2 (1C12) Mouse mAb。 | |
Immunohistochemical analysis of paraffin-embedded human lung carcinoma using Chk2 (1C12) Mouse mAb.免疫组织化学方法检测石蜡包埋人类肺癌组织,使用的抗体为Chk2 (1C12) Mouse mAb。 |