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030286 Mouse Anti-GYS1 (Glycogen Synthase 1)

Specifications
References
Clone Type
Monoclonal
Host
Mouse
Source
Human
Swiss Prot
P13807
Isotype
IgG1
Clone Number
13B364 (3A7)
Grade
Ascites
Applications
E FC WB
Crossreactivity
Hu
Gene ID
2997
Shipping Temp
Blue Ice
Storage Temp
-20°C
GSY; GYS; GYS1

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.

Applications
Suitable for use in Flow Cytometry, ELISA and Western Blot. Other applications not tested.
Recommended Dilutions
Flow Cytometry: 1:200-1:400 ELISA: 1:10,000 Western Blot: 1:500-1:2000 Optimal dilutions to be determined by the researcher.
Storage and Stability
May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Immunogen
Purified recombinant protein fragment corresponding to aa578-737 from human GYS1, expressed in E. coli
Form
Supplied as a liquid, 0.03% sodium azide.
Purity
Ascites
Specificity
Recognizes human GYS1
References
1. PLoS One. 2007 Mar 14;2(3):e285. 2. Mol Syst Biol. 2007; 3:89. Epub 2007 Mar 13.
USBio References
No references available
Conjugates
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