Anti-Glycogen synthase 1 / GYS1 Antibody [SN75-05]
ET1611-59
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse
TargetGYS1
Overview
- SupplierHUABIO
- Product NameAnti-Glycogen synthase 1 / GYS1 Antibody [SN75-05]
- Delivery Days Customer7
- ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
- Applications SupplierWB,IF-Cell,IF-Tissue,IHC-P,FC,IP
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDSN75-05
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID2997
- Target nameGYS1
- Target descriptionglycogen synthase 1
- Target synonymsGSY, GYS, glycogen [starch] synthase, muscle, glycogen synthase 1 (muscle)
- HostRabbit
- IsotypeIgG
- Protein IDA2RRU1
- Protein NameGlycogen [starch] synthase, muscle
- Scientific DescriptionGlycogen [starch] synthase belongs to the mammalian/fungal glycogen synthase family of proteins. Two forms of this protein exist, a liver form and a muscle form, both of which have the same function in the glycogen biosynthesis pathway. Glycogen synthase transfers the glycosyl residue from UDP-Glucose to the nonreducing end of alpha-1,4-glucan. The liver glycogen synthase protein is truncated by 34 amino acids compared to the muscle form. However, these enzymes differ significantly in their amino- and carboxyl-terminal regions. Muscle glycogen synthase serves to fuel muscular activity only and is regulated by muscle contraction and by catecholamines. Liver glycogen synthase mediates blood glucose homeostasis in response to nutritional cues. Defects in the gene encoding liver glycogen synthase results in glycogen storage disease type 0 (GSD0), a rare form of fasting ketotic hypoglycemia.
- ReactivityHuman, Mouse
- Reactivity SupplierHuman,Mouse
- Reactivity Supplier NoteRat
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC41116161