|
| 产地 | |
| 品牌 | 国产 |
| 货号 | |
| 用途 | 科研实验 |
| 英文名称 | Anti-GBA Polyclonal Antibody |
| 包装规格 | |
| 纯度 | % |
| CAS编号 | |
| 保质期 | 一年 |
| 是否进口 | 否 |
| 英文名称 | Anti-GBA Polyclonal Antibody |
|---|---|
| 宿主 | Rabbit |
| 别名 | GBA1;GCB;GLUC |
| 应用 | WB IHC |
| 稀释比例 | WB 1:500-2000. IHC 1:50-200. |
| 交叉反应 | Human |
| 蛋白分子量 | 60kDa |
| Gene ID | 2629 |
| 保存 | Store at -20°C. Avoid freeze / thaw cycles. |
| 储存液 | Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| 纯化方法 | Affinity purification |
| 亚型 | IgG |
| 免疫原 | Recombinant protein of human GBA |
| 性状 | 液体 |
| Public Immunogen Range | Recombinant protein of human GBA |
| Subcellular Locations | Lumenal side Lysosome membrane Peripheral membrane protein |
| Swiss Prot | P04062 |
| 克隆类型 | Polyclonal Antibody |
| 背景资料 | This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. |
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