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Ultrathin sections were made using a Diatome diamond knife mounted on a Reichert ultramicrotome and placed on copper TEM grids.
Serial ultrathin sections from each of the species were cut with a diamond knife, mounted on Cu grids, stained in uranyl acetate and lead citrate, and then observed under a Philips CM 10 (FEI, Eindhoven, The Netherlands) transmission electron microscope (TEM) operating at 80 kV.
Thin (∼90 nm thick) sections were cut with a diamond knife, mounted on copper grids, double stained with uranyl acetate and lead citrate [51].
Embedded samples were first trimmed with a razor blade and then 2 µm thick sections were cut using a glass knife mounted on an ultrotome.
Semi-thin sections (around 2 µm) were cut with a glass knife, mounted on microscope slides, stained with 0.1% boracic toluidine blue and used to study the histology and for localization of appropriate sites for ultrastructural analysis.
Ultrathin (50 70 nm) conventional sections were cut using a diamond knife mounted to a Reichart Ultracut S ultramicrotome.
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Rotary plows or tillers (sometimes called rototillers) have curved cutting knives mounted on a horizontal power-driven shaft.
One-micrometer thick sections of the apical and basal-coil cochlear cultures were cut from the plastic blocks with glass knives, mounted on glass slides and either stained with Toluidine blue or coated with Ilford L4 Nuclear Research Emulsion (Ilford Imaging UK Limited, Mobberley, Cheshire) for autoradiography.
Meat revolves in a bowl and passes through a set of knives mounted on a high-speed rotating arbor in a fixed position.
The samples were cut with a surgery knife and mounted on aluminum holders.
Semi-thin (300 nm) sections were cut on a Reichert-Jung Ultracut E microtome equipped with a diamond knife and mounted onto silane-coated microscope slides for light microscopy.
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