Glycogen Synthase 1 (phospho Ser645) rabbit pAb

Glycogen Synthase 1 (phospho Ser645) rabbit pAb

AO-06-ES5702-100

Glycogen Synthase 1 (phospho Ser645) rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES5702
Product nameGlycogen Synthase 1 (phospho Ser645) rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameGYS1; GYS; Glycogen [starch] synthase; muscle
Size100μL
Unit price ($)248
Human gene ID2997
Human Swiss-ProtP13807
SourceRabbit
IsotypeIgG
TargetGlycogen Synthase 1
Fields>>Starch and sucrose metabolism;>>Metabolic pathways;>>PI3K-Akt signaling pathway;>>AMPK signaling pathway;>>Insulin signaling pathway;>>Glucagon signaling pathway;>>Insulin resistance;>>Diabetic cardiomyopathy
Gene nameGYS1
Protein nameGlycogen [starch] synthase muscle
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14936
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9Z1E4
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID690987
Rat gene linkView Rat Gene
Rat Swiss-ProtA2RRU1
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human Glycogen Synthase around the phosphorylation site of Ser645. AA range:611-660
SpecificityPhospho-Glycogen Synthase 1 (S645) Polyclonal Antibody detects endogenous levels of Glycogen Synthase 1 protein only when phosphorylated at S645.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/5000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)83kD
BackgroundThe 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],
Functioncatalytic activity:UDP-glucose ((1->4)-alpha-D-glucosyl)(n) = UDP + ((1->4)-alpha-D-glucosyl)(n+1).,disease:Defects in GYS1 are the cause of muscle glycogen storage disease type 0 (GSD0b) [MIM:611556]; also called muscle glycogen synthase deficiency. GSD0 is a metabolic disorder characterized by fasting hypoglycemia presenting in infancy or early childhood. The role of muscle glycogen is to provide critical energy during bursts of activity and sustained muscle work.,enzyme regulation:Allosteric activation by glucose-6-phosphate. Phosphorylation reduces the activity towards UDP-glucose. When in the non-phosphorylated state, glycogen synthase does not require glucose-6-phosphate as an allosteric activator; when phosphorylated it does.,function:Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan.,pathway:Glycan biosynthesis; glycogen biosynthesis.,similar
Subcellular locationcytosol,membrane,inclusion body,
ExpressionEndometrium,Heart,Kidney,Lymph,Muscle,Skin,

Additional Images

Image 1
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Western Blot analysis of 293 cells using Phospho-Glycogen Synthase 1 (S645) Polyclonal Antibody
Image 2
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Enzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using Glycogen Synthase (Phospho-Ser645) Antibody
Image 3
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Immunohistochemistry analysis of paraffin-embedded human skeletal muscle, using Glycogen Synthase (Phospho-Ser645) Antibody. The picture on the right is blocked with the phospho peptide.
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Western blot analysis of lysates from NIH/3T3 cells treated with PMA 125ng/ml 30', using Glycogen Synthase (Phospho-Ser645) Antibody. The lane on the right is blocked with the phospho peptide.
: AO-06-ES5702-100
: 10 Produits
Hurry! only 10 items left in stock.

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