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Cat. No.: DPP-001084
| Product Overview | |
|---|---|
| Species | Human |
| Format | Lyophilized |
| Purity | ≥ 70% by HPLC |
| Nature | Synthetic |
| Target Information | |
|---|---|
| Gene Name | GYS1 |
| UniProt No. | P13807 |
| Gene ID | 2997 |
| Alternative Names | Glycogen [starch] synthase; Glycogen synthase 1; Glycogen synthase 1 (muscle); GSY; GYS; Gys1; GYS1_HUMAN; muscle |
| Function | Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan. |
| Involvement In Disease | Defects in GYS1 are the cause of muscle glycogen storage disease type 0 (GSD0b); also known as muscle glycogen synthase deficiency. GSD0b is a metabolic disorder characterized by fasting hypoglycemia presenting in infancy or early childhood. The role of muscle glycogen is to provide critical energy during bursts of activity and sustained muscle work. |
| Sequence | YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE,Belongs to the glycosyltransferase 3 family. |
| Shipping & Storage | |
|---|---|
| Shipping | Shipped on dry ice. |
| Storage | Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle. |
Ace Therapeutics has a team of experts in the field of endocrine and metabolic research, aiming to provide innovative preclinical contract research solutions to cope with diabetes and its complications. We provide customized solutions and technical support, enabling the transformation of promising concepts into innovative treatments, thus accelerating the drug development process of diabetes.
