Western blot analysis of extracts of HeLa cells, using Anti-EXOC1 Antibody (A87895) at 1:3,000 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 Enhanced Kit (RM00021). Exposure time: 90s.
Western blot analysis of extracts of mouse brain, using Anti-EXOC1 Antibody (A87895) at 1:3,000 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: 90s.
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Proteins predicted to interact with EXOC1
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.
