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After dehydration, each specimen was embedded by infiltration in Spurr's medium.
Each specimen was embedded in paraffin and cut into 3 µm serial sections, stained with hematoxylin eosin and subjected to histopathological examination by light microscopy.
Thereafter, each specimen was embedded in paraffin.
The biopsy specimen was embedded non-decalcified into methylmethacrylate.
Each specimen was embedded in Epon812 for transmission electron microscopy (TEM).
The obtained specimen was embedded into OCT (Optimal Cutting Temperature) compound and immediately frozen in liquid N2.
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The images are created after a specimen is embedded in gelatin, sliced into microscopic sections and digitized.
Specimen were embedded in tissue-tek and quick-frozen in fluid nitrate.
The larger part of the resected specimens was embedded in formalin-fixed paraffin blocks and used for histopathological examinations.
After dehydration through gradient ethanol solutions, the specimens were embedded in Araldite-Epon (Embed-812, Electron Microscopy Sciences, USA).
After dehydration through the gradient ethanol solutions, the specimens were embedded in Araldite-Epon (Embed-812, Electron Microscopy Sciences, Hatfield, PA, USA).
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