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Agnoprotein dysregulates U937 surface marker expression during differentiation. U937 cells were seeded in 2-well tissue culture chamber slides and induced for differentiation with PMA. Simultaneously, cells were treated with CM-control (upper panel) or CM-agnoprotein (lower panel). At 72 hours, cells were fixed and processed for immunocytochemistry for CD16 (A), CD68 (B), or CD71 (C).
