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Immunocytochemical staining of HepG2 cells with SMAC antibody . Nuclei were stained blue with DAPI; SMAC was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: High. Scale bar, 20 μm.
Western blotting analysis using DIABLO antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with DIABLO antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using NaQ™ ECL Substrate Kit .
Western blotting analysis using SMAC antibody . SMAC expression in wild-type (WT) and DIABLO knockout (KO) 293T cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with SMAC antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using NaQ™ ECL Substrate Kit .
Flow cytometric analysis of SMAC expression in HepG2 cells using SMAC antibody . Green, isotype control; red, SMAC.





