Western blotting analysis using MRPS26 antibody (Cat#65321). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with MRPS26 antibody (Cat#65321, 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 MRPS26 antibody (Cat#65321). MRPS26 expression in wild-type (WT) and MRPS26 shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with MRPS26 antibody (Cat#65321, 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).
Flow cytometric analysis of MRPS26 expression in HAP-1 cells using MRPS26 antibody (Cat#65321, 1:2,000). Green, isotype control; red, MRPS26.
Validation of MRPS26 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with MRPS26 antibody (Cat#65321, 1:2,000) and analyzed using BD flow cytometer.
Immunocytochemical staining of HAP-1 cells with MRPS26 antibody (Cat#65321, 1:1,000). Nuclei were stained blue with DAPI; MRPS26 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.
