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Tissue blocks were sectioned on a Leica CM3050 S cryostat.
Methacrylate blocks were sectioned on an MT-990 microtome (Boeckeler Instruments, Tucson, AZ, USA).
Blocks were sectioned on a Leica ultramicrotome, placed on grids and examined in a Phillips H-100 electron microscope.
Embedded blocks were sectioned on a Struers Accutom-50 precision cut-off saw (Struers, Copenhagen, Denmark) using a R330 diamond wafered wheel under water irrigation.
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Paraffin blocks were sectioned to 4 μm thickness and placed on positively charged glass slides.
TMA blocks were sectioned to produce 4-µm sections.
The TMA recipient block was sectioned on a routine microtome machine.
Tissue blocks were sectioned, mounted on glass slides, deparaffinised, and stained with haematoxylin and eosin.
Paraffin-embedded blocks were sectioned, mounted on Superfrost plus slides, de-waxed, and then brought to water.
Paraffin-embedded blocks were sectioned and mounted on frost-free slides.
Blocks were sectioned and put on poly-1-lysine coated slides.
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