WB
Western blot analysis of PUS7 using anti-PUS7 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-PUS7 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 PUS7 using anti-PUS7 antibody.
PUS7 was detected in a paraffin-embedded section of human colon
cancer tissue. The tissue section was incubated with rabbit anti-PUS7
Antibody at a dilution of 1:200 and developed using HRP
Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen
IHC
HC analysis of PUS7 using anti-PUS7 antibody.
PUS7 was detected in a paraffin-embedded section of mouse bladder tissue. The tissue section was incubated with rabbit anti-PUS7 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 PUS7 using anti-PUS7 antibody.
PUS7 was detected in a paraffin-embedded section of rat bladder tissue. The tissue section was incubated with rabbit anti-PUS7 Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IF-P
IF analysis of PUS7 using anti-PUS7 antibody.
PUS7 was detected in a paraffin-embedded section of mouse bladder tissue. The tissue section was incubated with rabbit anti-PUS7 Antibody at a dilution of 1:100. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (red) was used as secondary antibody. The section was counterstained with DAPI (Blue).
ICC/IF
ICC/IF analysis of PUS7 using anti-PUS7 antibody and anti-Beta Tubulin antibody.
PUS7 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-PUS7 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 MCF-7 cells using anti-PUS7 antibody .
Overlay histogram showing MCF-7 cells stained with Rabbit polyclonal antibody to PUS7 (Blue line). To facilitate intrPUS7llular 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-PUS7 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.