WB
Western blot analysis of Importin Alpha 5/KPNA1 using anti-Importin Alpha 5/KPNA1 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HL-60 whole cell lysates,
Lane 2: human CACO-2 whole cell lysates,
Lane 3: human PC-3 whole cell lysates,
Lane 4: rat heart tissue lysates,
Lane 5: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Importin Alpha 5/KPNA1 antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate. A specific band was detected for Importin Alpha 5/KPNA1 at approximately 60 kDa. The expected band size for Importin Alpha 5/KPNA1 is at 60 kDa.
FC
Flow Cytometry analysis of U87 cells using anti-Importin Alpha 5/KPNA1 antibody.
Overlay histogram showing U87 cells stained with 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-Importin Alpha 5/KPNA1 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.
ICC/IF
ICC/IF analysis of Importin Alpha 5/KPNA1 using anti-Importin Alpha 5/KPNA1 antibody.
Importin Alpha 5/KPNA1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-Importin Alpha 5/KPNA1 Antibody at a dilution of 1:100. Fluoro488 Conjugated Goat Anti-Rabbit IgG (Green) was used as secondary antibody. The section was counterstained with DAPI (Blue).