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Cellular phenotype of caspase-3 positive cells. Double immunofluorescence was performed for cleaved caspase-3 (A) and anti-CD3 (B) on paw sections treated with sGal-9 30 μg, 24 hours after induction with CG. Panel C shows an overlay of the caspase-3 and anti-CD3 staining with co-localization indicated by arrowheads. D: DAPI was used as counterstain for cell nuclei. Scale bar = 150 μm.
