Research Article

Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A

Figure 3

Subcellular localization of ATP11A and three mutants in COS7 cells. (a) COS7 cells were transiently transfected with 3X-FLAg tagged WT or mutant ATP11A plasmids. Cells were double stained for FLAG and organelle marker GM130 or Calnexin (CANX). Nuclei were counter-stained with DAPI (blue). (b) Percentage of colocalization of ATP11A with GM130-marked Golgi (upper panel) and CANX-marked ER (lower panel) in COS7 cells. . ns: no statistical difference. Data are presented as the . Scale bars: 25 μm.
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