Sentence examples for blocks were cut using from inspiring English sources
The blocks were cut using a water-cooled diamond saw (Isomet 1000, Buheler Ltd ,Lake Bluff, IL, USA) at low speed.
Consecutive sections from these new paraffin blocks were cut using a rotary microtome (RM 2165, Leica, Wetzlar, Germany).
Representative 4 μm sections of tissue blocks were cut using a microtome, mounted onto poly-l-lysine-coated slides and dried overnight at 37 °C.
The TMA blocks were cut using a Leica Reichert-Jung BIOCUT 2035 microtome (Leica Biosystems, Wetzlar, Germany) in 5 μm sections.
Thereafter, bone blocks were cut using a bone saw (K 410, Kolbe GmbH, Elchingen, Germany) assuring a rim of at least 3 4 mm of adjacent bone at the side and at the bottom of the original bone defect.
Serial 4-μm sections of the paraffin blocks were cut using a cryotome and mounted on poly-L-lysine-coated slides that were fixed in hydrogen peroxide and 90% methanol.
Hardened blocked were cut using a Leica UltraCut UC7, 60 nm sections were collected onto formvar/carbon coated nickel grids and stained using 2% uranyl acetate and lead citrate.
These specimens were stored as paraffin-embedded tissue blocks and were cut, using a microtome, to provide tissue sections of 6 μm thickness and subsequently deparaffinised.
Tissue sections were set into paraffin wax blocks, 5 μm sections were cut using a microtome and fixed to poly-L-lysine-coated slides.
Then the femoral condyles were freed from the soft tissues and 1 × 1 cm blocks containing the original grafts were cut using a bone saw (K 410, Kolbe GmbH, Elchingen, Germany).
From these blocks, the following consecutive sections were cut using a rotary microtome (RM 2165, Leica, Germany): 1 × 3 μm section for HE staining, 20 × 10 μm sections for RNA extraction and real time PCR (see below), 3 × 3 μm sections for immunohistochemistry (see below), 1 × 3 μm section for HE staining.
