Western blotting analysis using phospho-glycogen synthase 1 (S641) antibody (Cat#4127). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:1,000). Nuclei were stained blue with DAPI; Phospho-glycogen synthase 1 (S641) was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of phospho-glycogen synthase 1 (S641) expression in HepG2 cells using phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, phospho-glycogen synthase 1 (S641).
Western blotting analysis using phospho-glycogen synthase 1 (S641) antibody (Cat#4127). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:1,000). Nuclei were stained blue with DAPI; Phospho-glycogen synthase 1 (S641) was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of phospho-glycogen synthase 1 (S641) expression in HepG2 cells using phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, phospho-glycogen synthase 1 (S641).
Western blotting analysis using phospho-glycogen synthase 1 (S641) antibody (Cat#4127). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:1,000). Nuclei were stained blue with DAPI; Phospho-glycogen synthase 1 (S641) was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of phospho-glycogen synthase 1 (S641) expression in HepG2 cells using phospho-glycogen synthase 1 (S641) antibody (Cat#4127, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, phospho-glycogen synthase 1 (S641).
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