FUCA1 Polyclonal Antibody Store at -20°C
SKU: E-AB-15050-200
FUCA1 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-15050 |
| Reactivity | Human, Mouse |
| Host | Rabbit |
| Applications | WB, IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human FUCA1 |
| Abbre | FUCA1 |
| Synonyms | Alpha L fucosidase I, Alpha L fucoside fucohydrolase, Alpha-L-fucosidase 1, Alpha-L-fucosidase I, Alpha-L-fucoside fucohydrolase 1, FUCA, FUCA1, FUCO, Tissue alpha L fucosidase, Tissue alpha-L-fucosidase, alpha-L, alpha-L- 1, fucosidase, tissue |
| Swissprot | |
| Calculated MW | 54 kDa |
| Cellular Localization | Lysosome. |
| Concentration | 0.7 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Metabolism, Signal Transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
Related Reagents
| Applications | Recommended Dilution |
| WB | 1:500-1:2000 |
| IHC | 1:50-1:200 |
Background
The protein encoded by this gene is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids. Mutations in this gene are associated with fucosidosis (FUCA1D), which is an autosomal recessive lysosomal storage disease. A pseudogene of this locus is present on chr 2.