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Fig. 1. RUNX1/AML1 and AML1-ETO are targeted to distinct subnuclear locations. Immunofluorescence microscopy for endogenous RUNX1/AML1 (red) and AML1-ETO (green) with DAPI staining (blue) in Kasumi-1 cells as well as merged images are shown. RUNX1/AML1 and AML1-ETO fusion protein are predominantly present in the nucleus but do not colocalize in the Kasumi-1 cells. An antibody detecting ETO was used to visualize the AML1-ETO fusion protein, whereas an antibody recognizing the C-terminal domain of RUNX1/AML1 was used to detect endogenous RUNX1/AML1.