| No | Size | Price | Availability | |
| ARP2629-01 | 50ul | 1500.00 | In Stock |  |
| ARP2629-01 | 100ul | 2000.00 | In Stock | |
| Source: | Rabbit | Gene Id: | 2629 |
| Isotype: | IgG | Swiss Prot: | P04062 |
| purity: | Affinity purification |
| Background: |
| 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. |
| Reactivity | Human |
| Tested applications | WB |
| Clonality | Polyclonal Antibody |
| Calculated MW | 60kDa |
| Recommended Dilutions |
WB 1:500-1:2000
|
| Immunogen | Recombinant protein of human GBA |
| Storage | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
| Synonym | GCB, GBA1, GLUC |
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