GYS2 / Unconjugated /
Product Details
Description | Specificity of human, mouse Glycogen synthase 2 antibody verified on a Protein Array containing target protein plus 383 other non-specific proteins. | |
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Conjugate | Unconjugated | |
Clone | ||
Target Species | Human | |
Applications | IHC-P, WB, IHC | |
Supplier | Novus Biologicals | |
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Antigen | ||
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About GYS2
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. [provided by RefSeq, Dec 2009]
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. [provided by RefSeq, Dec 2009]
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Validation References
PMID 23436904 | |
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Additional Sources |
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78 GYS2 antibodies from over 12 suppliers available with over 21 conjugates.