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GBA Monoclonal Antibody (OTI1C7), TrueMAB™, OriGene
Mouse Monoclonal Antibody
Supplier: OriGene TA803363
Description
GBA 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.Specifications
| GBA | |
| Monoclonal | |
| 1 mg/mL | |
| PBS with 1% BSA, 50% glycerol and 0.02% sodium azide | |
| P04062 | |
| GBA | |
| Human recombit protein fragment corresponding to amino acids 40-315 of human GBA produced in E.coli. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG1 |
| Western Blot | |
| OTI1C7 | |
| Unconjugated | |
| GBA | |
| GBA1, GCB, GLUC | |
| Mouse | |
| Affinity Chromatography | |
| RUO | |
| 2629 | |
| -20° C, Avoid Freeze/Thaw Cycles | |
| Liquid |
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