Western blotting analysis using Signal recognition particle 19 antibody (Cat#2748). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Signal recognition particle 19 antibody (Cat#2748, 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).
Immunocytochemical staining of HepG2 cells with Signal recognition particle 19 antibody (Cat#2748, 1:1,000). Nuclei were stained blue with DAPI; Signal recognition particle 19 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 Signal recognition particle 19 expression in HepG2 cells using Signal recognition particle 19 antibody (Cat#2748, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, Signal recognition particle 19.
Western blotting analysis using Signal recognition particle 19 antibody (Cat#2748). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Signal recognition particle 19 antibody (Cat#2748, 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).
Immunocytochemical staining of HepG2 cells with Signal recognition particle 19 antibody (Cat#2748, 1:1,000). Nuclei were stained blue with DAPI; Signal recognition particle 19 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 Signal recognition particle 19 expression in HepG2 cells using Signal recognition particle 19 antibody (Cat#2748, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, Signal recognition particle 19.
Western blotting analysis using Signal recognition particle 19 antibody (Cat#2748). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Signal recognition particle 19 antibody (Cat#2748, 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).
Immunocytochemical staining of HepG2 cells with Signal recognition particle 19 antibody (Cat#2748, 1:1,000). Nuclei were stained blue with DAPI; Signal recognition particle 19 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 Signal recognition particle 19 expression in HepG2 cells using Signal recognition particle 19 antibody (Cat#2748, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, Signal recognition particle 19.
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