Flow cytometric analysis of IKK alpha expression in HepG2 cells using anti-IKK alpha antibody (Cat#61374, 1:2,000). Green, isotype control; red, IKK alpha.
Immunocytochemical staining of HepG2 cells with anti-IKK alpha antibody (Cat#61374, 1:1,000). Nuclei were stained blue with DAPI; IKK alpha 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 anti-IKK α antibody (Cat#61374). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-IKK α antibody (Cat#61374,1:20,000) and HRP-conjugated goat anti rabbit secondary antibody (Cat#201,1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-IKK alpha antibody (Cat#61374). IKK alpha expression in wild type (WT) and IKK alpha shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with anti-IKK alpha antibody (Cat#61374,1:20,000) and HRP-conjugated goat anti rabbit secondary antibody (Cat#201,1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Validation of IKK alpha knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-IKK alpha antibody (Cat#61374, 1:2,000) and analyzed using BD flow cytometer.
Immunocytochemical staining of HeLa cells using anti-IKK alpha antibody (Cat#61374, 1:1,000), Top panel: wild-type (WT); Bottom panal: IKK alpha shRNA knockdown (KD). Nuclei were stained blue with DAPI; IKKalpha was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm. Permeabilization: Triton.