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Flow cytometric analysis of forkhead box A1 expression in HepG2 cells using forkhead box A1 antibody . Green, isotype control; red, forkhead box A1.
Immunocytochemical staining of HepG2 cells with Forkhead box A1 antibody . Nuclei were stained blue with DAPI; Forkhead box A1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.
Western blotting analysis using Forkhead box A1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with Forkhead box A1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using FeQ™ ECL Substrate Kit .
Western blotting analysis using forkhead box A1 antibody . Forkhead box A1 expression in wild-type (WT) and forkhead box A1 (FOXA1) shRNA knockdown (KD) HepG2 cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with forkhead box A1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using FeQ™ ECL Substrate Kit .
Validation of forkhead box A1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HepG2 cells were stained with forkhead box A1 antibody and analyzed using BD flow cytometer.
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