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The recombinant antibody against GYS1 was produced using a synthesized peptide derived from Human Phospho-GYS1 (S641) as the immunogen. This antibody exists as a non-conjugated isotype Rabbit IgG, Affinity-chromatography purified. This antibody has been validated on ELISA, WB, IF.
The recombinant antibody against GYS1 was produced using a synthesized peptide derived from Human Phospho-GYS1 (S641) as the immunogen. This antibody exists as a non-conjugated isotype Rabbit IgG, Affinity-chromatography purified. This antibody has been validated on ELISA, WB, IF.
$350.00
| Cat.No | ADC-56304A | Clonality | Monoclonal |
|---|---|---|---|
| Target Name | GYS1 | Target Synonyms | Glycogen [starch] synthase antibody; Glycogen synthase 1 (muscle) antibody; Glycogen synthase 1 antibody; GSY antibody; GYS antibody; Gys1 antibody; GYS1_HUMAN antibody; muscle antibody |
| Form | Liquid | Species Reactivity | Human |
| Isotype | Rabbit IgG | Storage Buffer | PH 7.4, 0.02% sodium azide and 50% glycerol., 150mM NaCl, Rabbit IgG in phosphate buffered saline |
| Purification Method | Affinity-chromatography purified | Conjugate | Non-conjugated |
| Application | ELISA, IF, WB | Storage | Upon receipt |
| Immunogen Description | A synthesized peptide derived from Human Phospho-GYS1 (S641) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | P13807 |
Uniprot Id
P13807
Target Species
Human
Target Name
GYS1
Target Full Name
Glycogen [starch] synthase, muscle
Target Function
Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan.
Target Involvement
Muscle glycogen storage disease 0 (GSD0b)
Target Protein Families
Glycosyltransferase 3 family
Target Synonyms
Glycogen [starch] synthase; Glycogen synthase 1 (muscle); Glycogen synthase 1; GSY; GYS; Gys1; GYS1_HUMAN; muscle
Target Background
The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1, 4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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