31 products were found matching "GeneID 2997"!

Antibody in PBS with 0.02% sodium azide, 50% glycerol and 0.4-0.5mg/ml BSA. The protein encoded by the GYS1 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...

Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]

Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]

Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]

Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]

This affinity purified antibody is directed against human muscle glycogen synthase. The product was affinity purified from monospecific antiserum by immunoaffinity purification. Antiserum was first purified against the phosphorylated form of the immunizing peptide. The resultant affinity purified antibody was then...

This affinity purified antibody is directed against human muscle glycogen synthase. The product was affinity purified from monospecific antiserum by immunoaffinity purification. Antiserum was first purified against the phosphorylated form of the immunizing peptide. The resultant affinity purified antibody was then...

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...

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...

Transfers the glycosyl residue from UDP-Glc to the non-reducing end of a-1,4-glucan. Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]

Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]

Transfers the glycosyl residue from UDP-Glc to the non-reducing end of a-1,4-glucan. Protein function: Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. [The UniProt Consortium]