Western blotting analysis using CFAP298 antibody (Cat#5395). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with CFAP298 antibody (Cat#5395, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunocytochemical staining of HepG2 cells with CFAP298 antibody (Cat#5395, 1:1,000). Nuclei were stained blue with DAPI; CFAP298 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain:. Scale bar, 20 μm.
Flow cytometric analysis of CFAP298 expression in HepG2 cells using CFAP298 antibody (Cat#5395, 1:1,000). Green, isotype control; red, CFAP298.
Western blotting analysis using CFAP298 antibody (Cat#5395). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with CFAP298 antibody (Cat#5395, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunocytochemical staining of HepG2 cells with CFAP298 antibody (Cat#5395, 1:1,000). Nuclei were stained blue with DAPI; CFAP298 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain:. Scale bar, 20 μm.
Flow cytometric analysis of CFAP298 expression in HepG2 cells using CFAP298 antibody (Cat#5395, 1:1,000). Green, isotype control; red, CFAP298.
Western blotting analysis using CFAP298 antibody (Cat#5395). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with CFAP298 antibody (Cat#5395, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Immunocytochemical staining of HepG2 cells with CFAP298 antibody (Cat#5395, 1:1,000). Nuclei were stained blue with DAPI; CFAP298 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain:. Scale bar, 20 μm.
Flow cytometric analysis of CFAP298 expression in HepG2 cells using CFAP298 antibody (Cat#5395, 1:1,000). Green, isotype control; red, CFAP298.
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