Western blot analysis of extracts of various cell lines, using Anti-ERO1LB Antibody (A11670) at 1:1,000 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: 5s.
Proteins predicted to interact with ERO1LB
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.