FIG 3.

Association of NFATc2 with Zta in cells. Akata cells were induced to enter the lytic cycle for 24 h following exposure to anti-IgG, and proteins were extracted and analyzed as the input. Extracts were subjected to immunoprecipitation with the indicated antibodies and isotype controls and then analyzed by Western blotting for the proteins shown. (A) Immunoprecipitation with Zta antibody. (B) Immunoprecipitation antibody for EBF1. (C) Immunoprecipitation antibody with LEF1 antibody. The migration of molecular weight markers (in kilodaltons) is shown on the left.