Western blot analysis of extracts of THP-1 cells, using Anti-RASGRP1 Antibody (A8633) 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: 30s.
Immunofluorescence analysis of A-549 cells using Anti-RASGRP1 Antibody (A8633) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of C6 cells using Anti-RASGRP1 Antibody (A8633) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of NIH/3T3 cells using Anti-RASGRP1 Antibody (A8633) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
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Proteins predicted to interact with RASGRP1
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.
