GALT Polyclonal Antibody (E-AB-15057)
For research use only.
| Verified Samples |
Verified Samples in WB: Human liver Verified Samples in IHC: Human tonsil, Human brain |
| Dilution | WB 1:500-1:2000, IHC 1:50-1:200 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human GALT |
| Abbre | GALT |
| Synonyms | GALT, Gal 1 P uridylyltransferase, Gal-1-P uridylyltransferase, Galactose 1 phosphate uridyl transferase, Galactose 1 phosphate uridylyltransferase, Galactose-1-phosphate uridylyltransferase, UDP glucose hexose 1 phosphate uridylyltransferase, UDP-glucose-- |
| Swissprot | |
| Calculated MW | 43 kDa |
| Cellular Localization | Cytosol, Golgi apparatus, Golgi apparatus. |
| Concentration | 0.3 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, 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. |
| background | Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene. |
Other Clones
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Other Formats
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Unconjugated
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