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Formalin-paraffin livers were cut into 5 μm thick.
The livers were cut out and snap frozen in liquid nitrogen.
Livers were cut into tissue blocks of 1 mm, transferred to new fixative solution and kept at 4°C overnight.
Cryostat sections of fixed and frozen rat livers were cut, treated and antibody-bound as described [ 17].
The excised livers were cut into separate portions for estimation of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPX), glutathione (GSH) and thiobarbituric reactive subatances (TBARS).
Cross sections of paraffin-embedded livers were cut (5 μm thicknesses) and stained with either hematoxylin and eosin (HE) for light microscopy examination [ 57] or Perl's reagent to reveal iron distribution [ 58].
Similar(54)
The lungs and liver were cut into 1.5 cm×1.5 cm×0.3 cm pieces for sectioning and the remainder of the tissue was preserved in liquid nitrogen for RNA isolation.
Small pieces of liver were cut and kept in 10% formalin solution for histological studies.
Flash-frozen muscle and formalin-fixed heart and liver were cut for staining.
Injured parts of the liver were cut into 3 mm thick slices.
Native liver and the decellularized liver were cut into small pieces, placed in centrifuge tubes, and, subsequently, lyophilized.
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