| 别名 | Forkhead box P3; Forkhead box protein P3; foxp3; |
| 基因名称 | FOXP3 |
| 蛋白名称 | FOXP3 |
| 推荐应用 | |
| 反应物种 | Human |
| 存储缓冲液 | PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA |
| Human Gene Link | 50943; |
| Human Swissprot No. | Q9BZS1 |
| Mouse Gene ID | 20371; |
| Mouse Swissprot No. | Q99JB6; |
| 特异性 | Endogenous |
| 稀释度 | WB 1:500~1:2000 |
| 参考分子量 | MW(Observed): 47 kDa |
| 预测分子量 | MW(Calculated): 47 kDa |
| 运输及保存条件 | -15°C to -25°C/1 year(Do not lower than -25°C) |
| 宿主 | Rabbit |
| 同种型 | IgG,Kappa |
| 背景介绍 | Defects in FOXP3 are the cause of immunodeficiency polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) [MIM:304790]; also known as X-linked autoimmunity-immunodeficiency syndrome. IPEX is characterized by neonatal onset insulin-dependent diabetes mellitus, infections, secretory diarrhea, trombocytopenia, anemia and eczema. It is usually lethal in infancy. |
| 细胞定位 | Nucleus, Cytoplasm. |
| 纯化 | Protein A |
| Clonality | Monoclonal |
| 修饰类型 | Unmodified |
| 细胞定位 | Nucleus, Cytoplasm. |
| 组织表达 | Thymus, Tonsil, Lymph node, Breast carcinoma, Lung cancer, Colorectal carcinoma |
周一至周日 8:00-18:00
