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Researchers use a microtome to cut a 65-yr-old woman's brain into 7,400 ultra-thin slices.
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Embedded brains were cut using a microtome to make 5 µM sections.
Donor corneal stromas were cut to 120 200 μm thickness slices using a microtome and then decellularized.
Mad scientists of an earlier era were content with using a microtome and glass slides to examine odd cell structures through a dusty lens.
Stem segments of at least 1 cm in length (including the stem base) were harvested, embedded in paraffin and sectioned using a microtome (10 µm sections).
Two or three 400 μm coronal sections were cut from each cortical region (mPFC or SCx) from one hemisphere using a microtome (Integraslice 7550 MM, Campden Instruments, IN).
Sections of 5-μm thickness were taken using a microtome (Leica RM 2135).
The slices were decalcified, dehydrated, fixed in paraffin and cut in 4 μm slices using a microtome.
At first, the layers of a multilayer sample must be separated using a microtome [8],[9] or a scalpel under a microscope.
However it was still possible to collect spectroscopic data without further sample preparation such as using a microtome to provide a smooth surface.
Fixed samples were dehydrated in a graded series of ethanols, embedded in Paraplast, and cut into 5-μm sections using a microtome (Leica RM 2265, Leica, Nussloch, Germany).
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