15 μg of HeLa lysate was run on 6-18% SDS-PAGE under reducing conditions and blotted onto nitrocellulose membrane. antibody at 1 μg/mL was used as the primary antibody and peroxidase conjugated goat anti-mouse IgG was used as the secondary antibody. TFAP2A band was visualized using ECL Western Blotting Substrate.

Result: antibody can detect TFAP2A by Western blotting.

IHC-P analysis of placenta tissue by TFAP2A antibody.
IHC-P was performed using sections of the formalin-fixed paraffin-embedded placenta tissue. Antigen was retrieved through addition of boiling Tris/EDTA buffer pH 9 in a pressure cooker for 3 min. Endogenous peroxidase activity was quenched by incubating the sections with 3% H₂O₂ for 30 min at room temperature. The sections were then incubated with TFAP2A antibody at 5 μg/mL at room temperature for 1 h. Poly-peroxidase conjugated goat anti-mouse IgG was used as the secondary antibody. Diaminobenzidine was used as the chromogen. The section was counterstained with hematoxylin. A tissue section incubated with phosphate-buffered saline followed by incubation with the secondary antibody was used as the background control.

Result: Trophoblastic cells are positively stained at the nuclei.

Immunoprecipitation was performed by incubation of 2.5 μg of antibody with HeLa lysate containing 200 μg of total protein. After absorption with Protein G beads, the mixture was run on 6-18% SDS-PAGE and blotted onto nitrocellulose membrane. TFAP2A (antibody) at 1 μg/mL was used as the primary antibody and peroxidase conjugated rabbit anti-mouse IgG (Light chain specific) was used as the secondary antibody.

Lane 1: HeLa lysate

Lane 2: TFAP2A immunoprecipitated from HeLa lysate by antibody

Lane 3: The same as Lane 2 but KT82 was used as IgG isotype control antibody

Result: antibody can immunoprecipitate TFAP2A.