GBA Mouse Monoclonal Antibody [Clone ID: UMAB171]
CAT#: UM800064CF
Carrier-free (BSA/glycerol-free) GBA mouse monoclonal antibody,clone UMAB171
Formulation: Standard
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CNY 4,999.00
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Specifications
Product Data | |
Clone Name | UMAB171 |
Applications | 10k-ChIP, IF, IHC |
Recommend Dilution | IHC 1:100~200 |
Reactivity | Human, Mouse, Rat |
Host | Mouse |
Clonality | Monoclonal |
Immunogen | Human recombinant protein fragment corresponding to amino acids 40-315 of human GBA (NP_000148) produced in E.coli. |
Formulation | Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose) |
Reconstitution Method | For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific) |
Purification | Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G) |
Conjugation | Unconjugated |
Storage Condition | Store at -20°C as received. |
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 |
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