Background:

The glycogen synthase 1 encoded by GYS1 catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in GYS1 are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for GYS1.

Classification:

Primary antibody

Alternative names:

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. AA range:621-670

Concentration:

1 mg/ml

Molecular weight:

83786

Applications:

WB, IHC-p, ELISA

Storage:

-20°C for one year

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