Western blot analysis of Mouse brain, using Anti-ATP13A2 Antibody (A88101) at 1:500 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 60s.
Immunofluorescence analysis of NIH/3T3 cells using Anti-ATP13A2 Antibody (A88101) at a dilution of 1:50 (40x lens). DAPI was used to stain the cell nuclei (blue).
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Proteins predicted to interact with ATP13A2
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.