WB
Western blot analysis of SOS1 using anti-SOS1 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-SOS1 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody.
IHC
IHC analysis of SOS1 using anti-SOS1 antibody.
SOS1 was detected in a paraffin-embedded section of human colon cancer tissue. The tissue section was incubated with rabbit anti-SOS1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of SOS1 using anti-SOS1 antibody.
SOS1 was detected in a paraffin-embedded section of mouse cerebellum tissue. The tissue section was incubated with rabbit anti-SOS1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of SOS1 using anti-SOS1 antibody.
SOS1 was detected in a paraffin-embedded section of rat cerebellum tissue. The tissue section was incubated with rabbit anti-SOS1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
FC
Flow Cytometry analysis of K562 cells using anti-SOS1 antibody.
Overlay histogram showing K562 cells stained with anti-SOS1 antibody (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SOS1 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 (Red line) was also used as a control.