| 货号 | 2197S |
| 反应种属 | Human |
| 来源宿主 | Rabbit |
| 应用 | W/IP/IHC-P/F |
| 使用方法 | WB(1:1000) IP (1:100) IHC-P (1:200) F (1:50) |
| 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 |
Flow cytometric analysis of untreated Jurkat cells, using Phospho-Chk2 (Thr68) (C13C1) Rb mAb versus propidium iodide (DNA content). The boxed population indicates phospho-Chk2 (Thr68)-positive cells.流式细胞术检测未处理的Jurkat细胞，使用的抗体为Phospho-Chk2 (Thr68) (C13C1) Rb mAb，PI染色法检测DNA含量作为对照。框内的细胞群为 phospho-Chk2 (Thr68)阳性细胞。 | |
Western blot analysis of extracts from HeLa cells, untreated or UV-treated, using Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb.Western blot方法检测未处理和紫外处理的HeLa细胞提取物，使用的抗体为Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb。 | |
Immunoprecipitation of phospho-chk2 from UV-treated HT29 cells using Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb followed by western blot using the same antibody.从HT29细胞中免疫沉淀phospho-chk2蛋白，使用的抗体为Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb，随后使用同一抗体进行western blot检测。 | |
Immunohistochemical analysis of paraffin-embedded human breast carcinoma using Phospho-Chk2 (Thr68) (C13C1) Rabbit 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Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb。 | |
Immunohistochemical analysis of paraffin-embedded human colon carcinoma, control (left) or λ phosphatase-treated (right), using Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb.免疫组织化学方法检测石蜡包埋人类结肠癌组织，对照组（左图）或λ 磷酸酶粗粒组（右图），使用的抗体为Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb。 | |
Immunohistochemical analysis of paraffin-embedded HT-29 cell pellets, control (left) or UV-treated (right), using Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb.免疫组织化学分析石蜡包埋HT-29细胞沉淀，对照组（左图）和紫外处理组（右图），使用的抗体为Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb。 | |
Immunohistochemical analysis of paraffin-embedded human lung carcinoma using Phospho-Chk2 (Thr68) (C13C1) Rabbit 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Phospho-Chk2 (Thr68) (C13C1) Rabbit mAb。 |
