WB
Western blot analysis of HNF4A using anti-HNF4A antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HNF4A antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
IHC
IHC analysis of HNF4A using anti-HNF4A antibody.
HNF4A was detected in a paraffin-embedded section of human liver cancer tissue. The tissue section was incubated with rabbit anti-HNF4A Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of HNF4A using anti-HNF4A antibody.
HNF4A was detected in a paraffin-embedded section of mouse intestine tissue. The tissue section was incubated with rabbit anti-HNF4A Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of HNF4A using anti-HNF4A antibody.
HNF4A was detected in a paraffin-embedded section of rat liver tissue. The tissue section was incubated with rabbit anti-HNF4A Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
ICC/IF
ICC/IF analysis of HNF-4-alpha using anti- HNF-4-alpha antibody.HNF-4-alpha was detected in immunocytochemical section of HEPG2 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 2μg/mL rabbit anti- HNF-4-alpha Antibody overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
FC
Flow Cytometry analysis of HEPG2 cells using anti- HNF-4-alpha antibody.Overlay histogram showing HEPG2 cells stained with PB9215 (Blue line).The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HNF-4-alpha Antibody (1:100) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (1:100) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.