|Application ||WB, FC, E|
|Description||Glycogen synthase, skeletal muscle, the rate limiting enzyme of the insulin-induced glycogenesis. 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. Muscle GS is expressed in several tissues.|
|Immunogen||Purified recombinant fragment of human GYS1 expressed in E. Coli.|
|Formulation||Ascitic fluid containing 0.03% sodium azide.|
|Other Names||Glycogen [starch] synthase, muscle, 220.127.116.11, GYS1, GYS|
WB~~1/500 - 1/2000
FC~~1/200 - 1/400
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||GYS1 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan.|
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Provided below are standard protocols that you may find useful for product applications.
1. PLoS One. 2007 Mar 14;2(3):e285. 2. Mol Syst Biol. 2007;3:89. Epub 2007 Mar 13.
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