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Acute brain slices were prepared 3 weeks after virus injection.
Brain slices were prepared from 29- to 35-day-old male rats; recording conditions were identical to those used in DA release studies.
Then the tissue block was fixated on a platform and 350-µm-thick brain slices were prepared using a Thermo scientific slicer (Microm HM 650 V) in ice-cold choline slicing solution.
Brain slices were prepared using established techniques [54].
Brain slices were prepared from Long-Evans rats and Thy1.2-EYFP mice following standard procedures.
Acute brain slices were prepared as previously described [11], [27] with minor modifications.
Similar(18)
Brain stem slices were prepared from adult (>160 g) Sprague Dawley rats (Charles River Laboratories, Inc., Wilmington, MA) as described in detail previously [5].
Brain tumor slices were prepared from 160 g female Fischer F344 rats sacrificed 2 weeks following initial 9L-luc tumor inoculation.
Coronal brain tissue slices were prepared from ICR mice and cultured in collagen gels as described previously (Miyata et al, 2001) with slight modifications.
Animals received a continuous infusion of cholesterol or vehicle for 14 days, after which they were sacrificed, their brains removed, and hippocampal slices were prepared for electrophysiological recordings as indicated.
The brain was then removed and 350-µm thick hippocampal–entorhinal slices were prepared using a vibratome (Leica VT 1200S).
More suggestions(15)
brain slices were mounted
brain slices were examined
brain slices were used
brain slices were exposed
brain slices were performed
brain cells were prepared
brain slices were verified
brain cortices were prepared
brain pericytes were prepared
brain slices were put
brain slices were made
brain extracts were prepared
brain lysates were prepared
brain sections were prepared
brain slices were stored
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