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Anti-GYS1 Antibody (7U169)
(Synonyms: muscle, Gys 1, GYS, GSY, Glycogen synthase 1, Glycogen [starch] synthase) Copy Product Info
🥰Excellent
Synonyms: muscle, Gys 1, GYS, GSY, Glycogen synthase 1, Glycogen [starch] synthase
Catalog No. TMAC-01693 Copy Product Info
🥰Excellent
Anti-GYS1 Antibody (7U169) is a Rabbit antibody targeting GYS1. Anti-GYS1 Antibody (7U169) can be used in FCM,ICC/IF,IHC,IP,WB.
Anti-GYS1 Antibody
(7U169)
(7U169)
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 50 μL | $296 | 7-10 days | 7-10 days | |
| 100 μL | $498 | 7-10 days | 7-10 days |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction
Bioactivity
Related Conjugates and Formulations
Antigen Details
Chemical Properties
Stability & Storage
| Description | Anti-GYS1 Antibody (7U169) is a Rabbit antibody targeting GYS1. Anti-GYS1 Antibody (7U169) can be used in FCM,ICC/IF,IHC,IP,WB. |
| Synonyms | muscle, Gys 1, GYS, GSY, Glycogen synthase 1, Glycogen [starch] synthase |
| Ig Type | IgG |
| Clone | 7U169 |
| Reactivity | Human,Mouse,Rat |
| Application | |
| Recommended Dose | WB: 1:1000; IHC: 1:50-200; ICC/IF: 1:50-200; FCM: 1:50-100 |
| Antibody Type | Monoclonal |
| Host Species | Rabbit |
| Construction | Recombinant Antibody |
| Purification | ProA affinity purified |
| Appearance | Liquid |
| Formulation | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
| Research Background | Glycogen [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 α-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. |
| Conjucates | Unconjugated |
| Immunogen | Recombinant Protein |
| Uniprot ID |
| Molecular Weight | Theoretical: 84 kDa. |
| Stability & Storage | Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
| Transport | Shipping with blue ice. |
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