POMT1 Polyclonal Antibody Store at -20°C
SKU: E-AB-13528-200
POMT1 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-13528 |
| Reactivity | Human |
| Host | Rabbit |
| Applications | IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human POMT1 |
| Abbre | POMT1 |
| Synonyms | Dolichyl phosphate mannose protein mannosyltransferase 1, Dolichyl phosphate mannose protein mannosyltransferase1, Dolichyl-phosphate-mannose--protein mannosyltransferase 1, LGMD2K, MDDGA1, MDDGB1, MDDGC1, POMT 1, POMT1, Prot, Protein O mannosyl transferase 1 |
| Swissprot | |
| Cellular Localization | Endoplasmic reticulum membrane. |
| Concentration | 0.4 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Neuroscience, 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 |
| IHC | 1:50-1:200 |
Background
The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.