WB
Western blot analysis of anti-PSIP1 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-PSIP1 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.
IHC
IHC analysis of PSIP1 using anti-PSIP1 antibody.
PSIP1 was detected in a paraffin-embedded section of human breast cancer tissue. The tissue section was incubated with rabbit anti-PSIP1 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 PSIP1 using anti-PSIP1 antibody.
PSIP1 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-PSIP1 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 PSIP1 using anti-PSIP1 antibody.
PSIP1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-PSIP1 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
ICC/IF
ICC/IF analysis of PSIP1 using anti-PSIP1 antibody and anti-Beta Tubulin antibody.
PSIP1 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-PSIP1 Antibody at a dilution of 1:100. Cy3-Conjugated Anti-rabbit IgG Secondary Antibody (Red) and Fluoro488-conjugated Anti-mouse IgG Secondary Antibody (Green) were used as secondary antibody.
FC
Flow Cytometry analysis of K562 cells using anti-PSIP1 antibody.
Overlay histogram showing K562 cells stained with anti-PSIP1 antibody (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSIP1 Antibody (1:100). Fluoro488 conjugated goat anti-rabbit IgG (1:100) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.