GALK1 Polyclonal Antibody
SKU: E-AB-11255-200
GALK1 Polyclonal Antibody
| SKU # | E-AB-11255 |
| 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 GALK1 |
| Abbre | GALK1 |
| Synonyms | EC 2.7.1.6, GALK, GALK 1, GALK1, GK1, GLK, GLK1, Galactokinase, Galactokinase 1, Galactose kinase, HEL-S-19, epididymis secretory protein Li 19 |
| Swissprot | |
| Calculated MW | 42 kDa |
| Cellular Localization | Cytosol, Extracellular region or secreted, extracellular exosome, Other locations: cytoplasm, membrane. |
| Concentration | 0.6 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Cell Biology, Epigenetics and Nuclear Signaling, 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
Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population.