Anti-GALT antibody
产品特性
| Product Cat#: | AB-06-4922 |
| Product type: | Primary antibody |
| Antigen: | GALT |
| Immunogen: | Synthetic peptide within human GALT aa 41-90/379. |
| Species immunized: | Rabbit |
| Isotype: | IgG |
| Applications: | Western Blot (1:400); Immunohistochemistry-Paraffin (1:200-400) |
| Reactivity: | Human, Mouse, Rat |
| Clonality (clone number): | Monoclonal, JE64-66 |
| Form: | Liquid |
| Buffer: | 1*TBS buffer (pH7.4), 0.05% BSA, 40% Glycerol, 0.05% NaN3. |
| Concentration: | 1 mg/ml |
| Purity: | Protein A affinity purified. |
| Storage: | Aliquot and freeze at -20°C. Avoid multiple freeze/thaw cycles. |
| Conjugate: | Unconjugated |
| Alternative names: | Gal 1 P uridylyltransferase antibody |
| Gal-1-P uridylyltransferase antibody | |
| Galactose 1 phosphate uridyl transferase antibody | |
| Galactose 1 phosphate uridylyltransferase antibody | |
| Galactose-1-phosphate uridylyltransferase antibody | |
| GALT antibody | |
| GALT_HUMAN antibody | |
| UDP glucose hexose 1 phosphate uridylyltransferase antibody | |
| UDP-glucose–hexose-1-phosphate uridylyltransferase antibody |
展开
靶标信息
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.
产品来源
洱畔科技实验室
