GYS2 Polyclonal Antibody Store at -20°C
SKU: E-AB-11276-200
GYS2 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-11276 |
| Reactivity | Human, Mouse, Rat |
| Host | Rabbit |
| Applications | IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human GYS2 |
| Abbre | GYS2 |
| Synonyms | EC 2.4.1.11, GYS2, Glycogen [starch] synthase, Glycogen starch synthase liver, Glycogen synthase 2 liver, Gys2, liver |
| Swissprot | |
| Cellular Localization | Cytoskeleton, cortical actin Cytoskeleton, Cytosol, Other locations: cell cortex, cytoplasm, ectoplasm. |
| 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. |
Related Reagents
| Applications | Recommended Dilution |
| IHC | 1:100-1:300 |
Background
The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.