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Exact(12)
Once the resin hardened, blocks were sectioned with an ultramicrotome (Leica).
Prepared tissue blocks were sectioned with cryostat at 5 microns thicknesses and collected on clean polysine™ glass slides.
Paraffin-embedded tissue blocks were sectioned with 4 μm thickness.
Frozen tissue blocks were sectioned with a cryomicrotome (Leica) at 4 5 μm thickness.
The tissue blocks were sectioned with a Leica Microtome and transferred to glass slides.
Blocks were sectioned with a Leica RM2235 rotary microtome at 12 µm.
Similar(48)
The embedded blocks were sectioned and incubated with 10% Alcian blue (Sigma-Aldrich) in 0.1 N HCl for 30 minutes.
The embedded tissue blocks were section with Shandon AS 325 rotary microtomes into approximately 5 μm thick section and slides were prepared with the sections.
Tissue blocks were sectioned 5 µm thick and stained with haematoxylin and eosin (H&E).
The vitrified block is sectioned at −140 to −160 °C with a diamond knife.
Each paraffin-embedded block was sectioned through its entirety and stained with H&E.
More suggestions(15)
blocks were formed with
blocks were incubated with
blocks were convolved with
blocks were administrated with
blocks were inked with
blocks were laid with
blocks were lined with
blocks were clogged with
blocks were flooded with
blocks were analyzed with
blocks were polymerized with
blocks were treated with
blocks were prepared with
blocks were demineralized with
blocks were smattered with
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