WB
Western blot analysis of SIGLEC15 using anti-SIGLEC15 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SIGLEC15 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using ECL Plus Western Blotting Substrate.
ICC/IF
ICC/IF analysis of SIGLEC15 using anti-SIGLEC15 antibody and anti-Beta Tubulin antibody.
SIGLEC15 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-SIGLEC15 Antibody at a dilution of 1:100. Fluoro488-conjugated Anti-rabbit IgG Secondary Antibody (green) and Cy3-conjugated Anti-mouse IgG Secondary Antibody (red) were used as secondary antibody.
FC
Flow Cytometry analysis of A549 cells using anti-SIGLEC15 antibody.
Overlay histogram showing A549 cells stained with Anti-SIGLEC15 Antibody (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SIGLEC15 Antibody at 1:100 dilution for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.