WB
Western blot analysis of CCDC36/IHO1 using anti-CCDC36/IHO1 antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates,
Lane 2: human HL-60 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CCDC36/IHO1 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 CCDC36/IHO1 using anti-CCDC36/IHO1 antibody.
CCDC36/IHO1 was detected in a paraffin-embedded section of human testis cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CCDC36/IHO1 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
IHC
IHC analysis of CCDC36/IHO1 using anti-CCDC36/IHO1 antibody.
CCDC36/IHO1 was detected in a paraffin-embedded section of human melanoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CCDC36/IHO1 Antibody at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) with DAB as the chromogen.
ICC/IF
ICC/IF analysis of CCDC36/IHO1 using anti-CCDC36/IHO1 antibody.
CCDC36/IHO1 was detected in an immunocytochemical section of SiHa cells. The section was incubated with rabbit anti-CCDC36/IHO1 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).