WB
Western blot analysis of Intersectin 1/ITSN1 using anti-Intersectin 1/ITSN1 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Caco-2 whole cell lysates,
Lane 2: human SiHa whole cell lysates,
Lane 3: human Hela whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Intersectin 1/ITSN1 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
IF analysis of Intersectin 1/ITSN1 using anti-Intersectin 1/ITSN1 antibody.
Intersectin 1/ITSN1 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-Intersectin 1/ITSN1 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).
FC
Flow Cytometry analysis of SiHa cells using anti-Intersectin 1/ITSN1 antibody.
Overlay histogram showing SiHa cells stained with anti-Intersectin 1/ITSN1 antibody. 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-Intersectin 1/ITSN1 Antibody (1:100). DyLight®488 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.