catalog number :
MBS850975
products full name :
GYS1 Antibody
products short name :
GYS1
products name syn :
GSY; GYS; GYS1
other names :
glycogen; Glycogen [starch] synthase, muscle; glycogen [starch] synthase, muscle; glycogen [starch] synthase, muscle; glycogen synthase 1 (muscle)
products gene name :
GYS1
other gene names :
GYS1; GYS1; GSY; GYS; GYS
uniprot entry name :
GYS1_HUMAN
form :
Ascitic fluid containing 0.03% sodium azide.
concentration :
100ug/100ul
tested application :
Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FC/FACS), ELISA (EIA)
app notes :
WB: 1/500 - 1/2000, FC: 1/200-1/400, ELISA: Propose dilution 1/10000. Not yet tested in other applications.
other info2 :
Immunogen: Purified recombinant fragment of human GYS1 expressed in E. Coli. Species: Mouse IgG1
products categories :
Cancer; Cardiovascular; Cell Biology; Epigenetics & Nuclear Signaling; Developmental Biologys; Immunology; Drug Discovery Products; Metabolism; Neuroscience; Signal Transduction; Stem Cells; Autophagy antibody
products description :
Background: 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.
ncbi acc num :
NP_001155059.1
ncbi gb acc num :
NM_001161587.1
ncbi pathways :
AMPK Signaling Pathway 198868!!AMPK Signaling Pathway 989139!!AMPK Signaling Pathway 992181!!Disease Pathway 530764!!Glucose Metabolism Pathway 106199!!Glycogen Metabolism Pathway 198856!!Glycogen Storage Diseases Pathway 980468!!Glycogen Synthesis Pathway 905990!!Insulin Signaling Pathway 198845!!Insulin Signaling Pathway 83090
ncbi summary :
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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]