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![Western Blot: Glycogen Synthase [p Ser641] Antibody [NB600-611] - Affinity Purified Glycogen Synthase [p Ser641] antibody.Lane 1: mouse cardiac myocyte lysate mock treated. Lane 2: mouse cardiac myocyte lysate insulin treated at 10nM for 15'.Lane 3: mouse cardiac myocyte lysate insulin treated at 100nM for 15'.Lane 4: mouse cardiac myocyte lysate insulin treated at 1nM for 15'.Lane 5: mouse cardiac myocyte lysate mock treated. Lane 6: mouse cardiac myocyte lysate CLA treated at 4nM for 45'. Lane 7: mouse cardiac myocyte lysate CLA treated at 20nM for 45'. Lane 8: mouse cardiac myocyte lysate CLA treated at 100nM for 45'. Load: 12uL. Primary Antibody: pS641 at 1:1000. Secondary Antibody: HRP conjugated Gt-a-Rabbit IgG at 1:5,000 dilution preceded color development using Amersham's substrate system. Other detection methods will yield similar results.](http://images.novusbio.com/fullsize/Glycogen-Synthase-[p-Ser641]-Antibody-Western-Blot-NB600-611-img0008.jpg "Western Blot: Glycogen Synthase [p Ser641] Antibody [NB600-611] - Affinity Purified Glycogen Synthase [p Ser641] antibody.Lane 1: mouse cardiac myocyte lysate mock treated. Lane 2: mouse cardiac myocyte lysate insulin treated at 10nM for 15'.Lane 3: mouse cardiac myocyte lysate insulin treated at 100nM for 15'.Lane 4: mouse cardiac myocyte lysate insulin treated at 1nM for 15'.Lane 5: mouse cardiac myocyte lysate mock treated. Lane 6: mouse cardiac myocyte lysate CLA treated at 4nM for 45'. Lane 7: mouse cardiac myocyte lysate CLA treated at 20nM for 45'. Lane 8: mouse cardiac myocyte lysate CLA treated at 100nM for 45'. Load: 12uL. Primary Antibody: pS641 at 1:1000. Secondary Antibody: HRP conjugated Gt-a-Rabbit IgG at 1:5,000 dilution preceded color development using Amersham's substrate system. Other detection methods will yield similar results.")
![Immunohistochemistry: Glycogen Synthase [p Ser641] Antibody [NB600-611] - Immunohistochemistry with Glycogen Synthase [p Ser641] antibody.Tissue: Human Prostate.Fixation: formalin-fixed, paraffin-embedded tissue.Antigen retrieval: heat-induced.Primary antibody: 5 ug/ml.Staining: antibody as precipitated red signal with a hematoxylin purple nuclear counterstain.](http://images.novusbio.com/fullsize/Glycogen-Synthase-[p-Ser641]-Antibody-Immunohistochemistry-NB600-611-img0009.jpg)
![Signal Stimulation: Glycogen Synthase [p Ser641] Antibody [NB600-611] - Diagram of glycogen synthase as a component of insulin signal transduction pathways.](http://images.novusbio.com/fullsize/Glycogen-Synthase-[p-Ser641]-Antibody-Signal-Stimulation-NB600-611-img0006.jpg)
![Western Blot: Glycogen Synthase [p Ser 641] Antibody (SR2258) [NBP3-21525] - Western blot analysis using NBP3-21525 in HeLa cell lysate.](http://images.novusbio.com/fullsize/nbp3-21525_rabbit-glycogen-synthase-p-ser-641-mab-sr2258-57202316112111.jpg "Western Blot: Glycogen Synthase [p Ser 641] Antibody (SR2258) [NBP3-21525] - Western blot analysis using NBP3-21525 in HeLa cell lysate.")
![Western Blot: Glycogen Synthase [p Ser641] Antibody (1D1) [NBP3-26421] - Positive Western Blot detected in Hela whole cell lysate, HepG2 whole cell lysate (treated with Calyculin A or EGF). All lanes: Glycogen Synthase [p Ser641] Antibody at 1.12ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 85 KDa Observed band size: 85 KDa](http://images.novusbio.com/fullsize/nbp3-26421_rabbit-glycogen-synthase-p-ser-641-mab-1d1-28220241148588.jpg "Western Blot: Glycogen Synthase [p Ser641] Antibody (1D1) [NBP3-26421] - Positive Western Blot detected in Hela whole cell lysate, HepG2 whole cell lysate (treated with Calyculin A or EGF). All lanes: Glycogen Synthase [p Ser641] Antibody at 1.12ug/ml. Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 85 KDa Observed band size: 85 KDa")
![Immunocytochemistry/Immunofluorescence: Glycogen Synthase [p Ser641] Antibody (1D1) [NBP3-26421] - Staining of HepG2 cells with Glycogen Synthase [p Ser641] Antibody (1D1) at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG (H+L).](http://images.novusbio.com/fullsize/nbp3-26421_rabbit-glycogen-synthase-p-ser-641-mab-1d1-282202412493634.jpg)