GYS2 Polyclonal Antibody

Background:
The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.

Research Area: Cancer, Metabolism, Signal Transduction

Synonyms:
EC 2.4.1.11, Glycogen [starch] synthase, Glycogen starch synthase liver, Glycogen synthase 2 liver, Gys2, GYS2, liver

Immunogen: Recombinant protein of human GYS2

Swissprot: P54840
Gene Accession: BC126310

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.2 mg/mL
Dilution: IHC 1:50-1:200

Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Alternative for product with catalog number:
sc-47109/sc-47106/sc-99029