Western blot analysis of extracts of various cell lines, using Anti-SLC5A7 Antibody (A10364) 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: 90s.
Immunofluorescence analysis of rat brain using Anti-SLC5A7 Antibody (A10364) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Proteins predicted to interact with SLC5A7
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.