WB
Western blot analysis of INF2 using anti-INF2 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-INF2 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 INF2 using anti-INF2 antibody.
INF2 was detected in a paraffin-embedded section of human colon cancer tissue. The tissue section was incubated with rabbit anti-INF2 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 INF2 using anti-INF2 antibody.
INF2 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-INF2 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 INF2 using anti-INF2 antibody.
INF2 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-INF2 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 INF2 using anti-INF2 antibody.
INF2 was detected in an immunocytochemical section of A549 cells. The section was incubated with rabbit anti-INF2 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).
WB
IP analysis of INF2 using anti-INF2 antibody in Hela whole cell lysate.
Western blot analysis of INF2 using anti- INF2 antibody.
Lane 1: Hela whole cell lysates(30ug),
Lane 2: Rabbit control IgG instead of anti- INF2 antibody in Hela whole cell lysate,
Lane 3: anti- INF2 antibody (2μg) + Hela whole cell lysate (500μg).
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti- INF2 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.