catalog number : 
MBS240567
products full name : 
Rabbit Polyclonal to Human GYS / GYS1
products short name : 
GYS / GYS1
products name syn : 
Anti-GYS / GYS1 Antibody (phospho-Ser640) IHC-plus; GYS1; Glycogen synthase 1 (muscle); GSY; GYS; Human GYS; GYS1
other names : 
glycogen; Glycogen [starch] synthase, muscle; glycogen [starch] synthase, muscle; glycogen [starch] synthase, muscle; glycogen synthase 1 (muscle)
products gene name syn : 
GYS1
other gene names : 
GYS1; GYS1; GSY; GYS; GYS
uniprot entry name : 
GYS1_HUMAN
specificity : 
Human Muscle Glycogen Synthase phospho peptide corresponding to a region of the human protein conjugated to Keyhole Limpet Hemocyanin (KLH).
purity : 
Immunoaffinity Purified
form : 
0.02 M potassium phosphate, 0.15 M sodium chloride, pH 7.2, 0.01% sodium azide.
storage stability : 
+4 degree C or -20 degree C, Avoid repeated freezing and thawing.
tested application : 
Immunohistochemistry (IHC - Paraffin), Western Blot (WB), Immunoprecipitation (IP), ELISA (EIA)
app notes : 
ELISA, IHC-P (5 ug/ml), IP, WB. Usage: Immunohistochemistry: was validated for use in immunohistochemistry on a panel of 21 formalin-fixed, paraffin-embedded (FFPE) human tissues after heat induced antigen retrieval in pH 6.0 citrate buffer. After incubation with the primary antib.
other info1 : 
Target Species: Human.  Immunogen Description: Phosphopeptide surrounding amino acid Ser640 from human glycogen synthase
other info2 : 
Antigen Modification: pSer640
ncbi acc num : 
NP_002094.2
ncbi gb acc num : 
NM_002103.4
ncbi mol weight : 
76,483 Da
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  1127581!!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]