Flow cytometric analysis of G3BP expression in HepG2 cells using G3BP antibody (Cat#3316, 1:2,000). Green, isotype control; red, G3BP.
Immunocytochemical staining of HepG2 cells with G3BP antibody (Cat#3316, 1:1,000). Nuclei were stained blue with DAPI; G3BP was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Scale bar: 20 μm.
Western blotting analysis using anti-G3BP antibody (Cat#3316). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G3BP antibody (Cat#3316, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Flow cytometric analysis of G3BP expression in HepG2 cells using G3BP antibody (Cat#3316, 1:2,000). Green, isotype control; red, G3BP.
Immunocytochemical staining of HepG2 cells with G3BP antibody (Cat#3316, 1:1,000). Nuclei were stained blue with DAPI; G3BP was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Scale bar: 20 μm.
Western blotting analysis using anti-G3BP antibody (Cat#3316). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G3BP antibody (Cat#3316, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Flow cytometric analysis of G3BP expression in HepG2 cells using G3BP antibody (Cat#3316, 1:2,000). Green, isotype control; red, G3BP.
Immunocytochemical staining of HepG2 cells with G3BP antibody (Cat#3316, 1:1,000). Nuclei were stained blue with DAPI; G3BP was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Scale bar: 20 μm.
Western blotting analysis using anti-G3BP antibody (Cat#3316). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G3BP antibody (Cat#3316, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
