Fig. 6.
Fig. 6. Binding of NFY is stabilized by the integrity of the adjacent c-myb binding site. EMSA was performed with the Y+M+ probe (lanes 1 to 3, 7, and 8), Y+M− probe (lanes 4 to 6), and +48/+80 probe (lanes 9 and 10). The reactions contained no protein (lanes 1, 4, 7, and 9) or 20 μg of RPMI-8402 nuclear extract (N.E.). In addition, reactions shown in lanes 3 and 6 contained anti-NFYA antibody (NFYA Ab; from Rockland Immunochemicals). The migration of NFY binding complex (NFY), supershifted complexes (s.s.), or free probe is shown by arrows. Nonspecific complexes are marked by stars.

Binding of NFY is stabilized by the integrity of the adjacent c-myb binding site. EMSA was performed with the Y+M+ probe (lanes 1 to 3, 7, and 8), Y+M− probe (lanes 4 to 6), and +48/+80 probe (lanes 9 and 10). The reactions contained no protein (lanes 1, 4, 7, and 9) or 20 μg of RPMI-8402 nuclear extract (N.E.). In addition, reactions shown in lanes 3 and 6 contained anti-NFYA antibody (NFYA Ab; from Rockland Immunochemicals). The migration of NFY binding complex (NFY), supershifted complexes (s.s.), or free probe is shown by arrows. Nonspecific complexes are marked by stars.

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