产品说明
一般描述
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. [provided by RefSeq, Jan 2010]
免疫原
A synthesized peptide derived from human Glucosylceramidase beta (Glucosylceramidase beta (GBA))
外形
Buffer: PBS with 0.02% sodium azide,0.05% BSA,50% glycerol,pH7.3.
产品性质
| 生物来源 | rabbit |
| 质量水平 | 100 |
| antibody product type | primary antibodies |
| 克隆 | monoclonal |
| 形式 | liquid |
| species reactivity | mouse, rat |
| 浓度 | 0.51 mg/mL |
| technique(s) | western blot: 1:500-1:2000 |
| UniProt登记号 | P04062 |
| 运输 | wet ice |
| 储存温度 | −20℃ |
| Gene Information | human ... GBA(2629) |
安全信息
| 闪点(F) | Not applicable |
| 闪点(C) | Not applicable |
Sigma-Aldrich
m.cnreagent.com
