GBA Mouse Monoclonal Antibody [Clone ID: OTI4G4]
CAT#: TA803377
GBA mouse monoclonal antibody, clone OTI4G4 (formerly 4G4)
Size: 30 ul
Formulation: Carrier Free
USD 436.00
Specifications
| Product Data | |
| Clone Name | OTI4G4 |
| Applications | IHC, WB |
| Recommended Dilution | WB 1:500, IHC 1:150 |
| Reactivities | Human, Mouse, Rat |
| Host | Mouse |
| Isotype | IgG2a |
| Clonality | Monoclonal |
| Immunogen | Human recombinant protein fragment corresponding to amino acids 40-315 of human GBA (NP_000148) produced in E.coli. |
| Formulation | PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide. |
| Concentration | 1 mg/ml |
| Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
| Conjugation | Unconjugated |
| Storage | Store at -20°C as received. |
| Stability | Stable for 12 months from date of receipt. |
| Predicted Protein Size | 55.5 kDa |
| Gene Name | glucosylceramidase beta |
| Database Link | |
| 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. [provided by RefSeq, Jan 2010] |
| Synonyms | GBA1; GCB; GLUC |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Lysosome, Metabolic pathways, Other glycan degradation, Sphingolipid metabolism |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
| Antibody Resources |
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