Western blot analysis of extracts of HeLa cells, using Anti-ZP3 Antibody (A90053) 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. Exposure time: 90s.
Immunofluorescence analysis of rat oophoroma cells using Anti-ZP3 Antibody (A90053) at a dilution of 1:100. DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of mouse oophoroma cells using Anti-ZP3 Antibody (A90053) at a dilution of 1:100. DAPI was used to stain the cell nuclei (blue).
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Proteins predicted to interact with ZP3
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.
