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Western blotting analysis using ATM antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with ATM antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using FeQ™ ECL Substrate Kit .
Western blotting analysis using ATM antibody . ATM expression in wild type (WT) and ATM knockdown (KD) 293T cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with ATM antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using FeQ™ ECL Substrate Kit .
Flow cytometric analysis of ATM expression in HepG2 cells using ATM antibody . Green, isotype control; red, ATM.
Immunocytochemical staining of HepG2 cells with ATM antibody . Nuclei were stained blue with DAPI; ATM 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.





