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.

Classification:

Primary antibody

Alternative names:

Glycogen [starch] synthase muscle; GYS1; GYS; Glycogen, starch; synthase; muscle

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

The antiserum was produced against synthesized peptide derived from human Glycogen Synthase around the phosphorylation site of Ser645. AA range:611-660

Concentration:

1 mg/ml

Molecular weight:

83786

Applications:

WB, IHC-p, IF, ELISA

Storage:

-20°C for 1 year

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