ab11512 stained in M158 cells. Cells were fixed with 100% methanol (5 min) at room temperature and incubated with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 1h at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody ab11512 at 10 µg/ml overnight at +4°C. The secondary antibody was ab150165 (colored green) used at 1 µg/ml for 1 hour at room temperature. DAPI was used to stain the cell nuclei (colored blue) at a concentration of 1.43 µM for 1hour at room temperature.

This data was developed using the same antibody clone in a different buffer formulation containing PBS, Azide and Arginine (ab11512).