靶标 CLCN7 别名 CLCN7;CLC-7;CLC7;OPTA2;OPTB4;PPP1R63 宿主 Rabbit 稀释比例 IHC 1:50-200. Gene ID 1186 保存 Store at -20°C. Avoid freeze / thaw cycles. Swiss Prot P51798 蛋白分子量 86/89kDa 储存液 Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3. 亚细胞定位 Cytoplasm 免疫原 A synthetic peptide of human CLCN7 亚型 IgG 纯化方法 Affinity purification 背景资料 The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. Public Immunogen Range 730-780/805aa 克隆类型 Polyclonal Antibody 交叉反应 Human Predicted:Cow Rat Mouse 应用 IHC 规格 50ul 100ul 使用前请离心。如有问题请及时联系我们。