WB
Western blot analysis of HHAT using anti-HHAT antibody. The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human U2OS whole cell lysates,
Lane 2: human SIHA whole cell lysates,
Lane 3: rat ovary tissue lysates,
Lane 4: rat testis tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HHAT 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
HHAT was detected in a paraffin-embedded section of human testis tissue. The tissue section was incubated with rabbit anti-HHAT 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
HHAT was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-HHAT Antibody at a dilution of 1:100. Cy3-Conjugated Anti-rabbit IgG Secondary Antibody (Red) and Fluoro488-conjugated Anti-mouse IgG Secondary Antibody (Green) were used as secondary antibody. The section was counterstained with DAPI (Blue).