Exact(8)
The deep temporalis fascia and the superficial muscle layer were transferred to construct a barrier, to support the function of the reconstructed ramus/condyle unit and to maintain flap vascularity.
Individual slices that displayed an intact dentate gyrus and pyramidal cell layer were transferred to sterile Millicell-CM (Millipore, Bedford, MA) membrane inserts (0.4 µm) in six-well culture plates with 1 ml growth medium.
After 10 min centrifugation at a rotation speed of 6000 g at 10°C, 300 µl of lipid extracts from the bottom layer were transferred into a new brown auto-sampler vial.
The patterns of the photoresist layer were transferred to the underlying Si substrates by reactive-ion etching (RIE).
Small pieces of the cell layer were transferred for distilled water for 10 min and finally collected onto copper grids (300 mesh).
After centrifugal separation at 3000 × g for 10 min, RBCs in the bottom layer were transferred into a new tube and stored at −70 °C until use.
Similar(52)
Thirty microliters of the ethyl acetate layer was transferred to glass GC vials, and the resulting preparation was injected into the GC column.
Subsequently, the aqueous upper layer was transferred to a fresh tube and 2 M NaCl (0.1 volumes) and absolute ethanol (2 volumes at -20 °C) were added.
After rinsing the graphene-PMMA with DI water, the layer was transferred onto a target substrate, followed by removal of PMMA by acetone.
The upper layer is transferred off in one direction and the lower in another; this cycle of operations may be repeated as many times as necessary to effect the desired separation.
The bottom chloroform layer was transferred to another tube.
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