At the end of treatment, mice were euthanized and the femur, spleen and liver were collected from each mouse and preserved in 10% neutral buffered formalin. Fixed tissues were processed to paraffin block and sectioned. Subsequent slides were stained with hematoxylin and eosin (H&E) and evaluated for changes in morphology. Additional sections from tissue sample were stained immunohistochemically with anti-human mitochondria membrane antibody (Millipore, MAB1273) at 1 μg/mL. The sections were counterstained with hematoxylin and examined by a Zeiss Axiophot microscope. Photos were acquired at 10X magnification for large panels and 40X magnification for the inserts.
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