Anti-Human/Mouse/Rat GYS2 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12049
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human GYS2
Specificity
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot P54840
Concentration 0.2 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names EC 2.4.1.11,Glycogen [starch] synthase,Glycogen starch synthase liver,Glycogen synthase 2 liver,Gys2,GYS2,liver
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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