Western blotting analysis using Aryl hydrocarbon receptor antibody (Cat#61360). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Aryl hydrocarbon receptor antibody (Cat#61360, 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).
Western blotting analysis using Aryl hydrocarbon receptor antibody (Cat#61360). Aryl hydrocarbon receptor expression in wild type (WT) and aryl hydrocarbon receptor shRNA knockdown (KD) Hela cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with Aryl hydrocarbon receptor antibody (Cat#61360, 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 Aryl hydrocarbon receptor antibody (Cat#61360, 1:1,000). Nuclei were stained blue with DAPI; Aryl hydrocarbon receptor 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 Aryl hydrocarbon receptor expression in HepG2 cells using Aryl hydrocarbon receptor antibody (Cat#61360, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, Aryl hydrocarbon receptor.
