Flow cytometric analysis of MARS1 expression in HT-1080 cells using anti-MARS1 antibody (Cat#65212, 1:2,000). Green, isotype control; red, MARS1.
Immunocytochemical staining of HT-1080 cells with anti-MARS1 antibody (Cat#65212, 1:1,000). Nuclei were stained blue with DAPI; MARS1 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-MARS1 antibody (Cat#65212). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MARS1 antibody (Cat#65212, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using anti-MARS1 antibody (Cat#65212). MARS1 expression in wild-type (WT) and MARS1 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-MARS1 antibody (Cat#65212, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Validation of MARS1 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-MARS1 antibody (Cat#65212, 1:2,000) and analyzed using BD flow cytometer.
Immunocytochemical staining of HeLa cells using anti-MARS1 antibody (Cat#65212, 1:1,000), Top panel: wild-type (WT); Bottom panal: MARS1 shRNA knockdown (KD). Nuclei were stained blue with DAPI; MARS1 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm.