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The incubated brain slices were washed in acidified KRB (pH = 5.0±0.2), rinsed 3 times with ice-cold KRB, and imaged.
Free-floating brain slices were washed in Tris-buffered saline (TBS) and pre-incubated in 3% goat normal serum (NGS) in TBS for 30 min. Cells were also fixed with 4% formaldehyde and rinsed in TBS.
At the end of the experiment, all the brain slices were washed in acidified KRB (pH = 5.0±0.2), rinsed 3 times with ice-cold KRB, and assayed for the radioactivity in a dual channel gamma counter (Perkin-Elmer, Waltham, MA).
Finally, the brain slices were washed in PBS and mounted in Mowiol mounting solution (Mowiol 4 88).
For labelling of DCX, brain slices were washed in PBS before incubation with 0.1% Triton X-100/PBS for 15 min on ice.
Brain slices were washed in 0.2 M sodium acetate and developed in DAB + nickel ammonium sulfate (17mg of DAB, 1.25 g Nickel ammonium sulfate in 50 ml of 0.2 M sodium acetate and 0.3% H2O2).
Similar(49)
Slices were washed and embedded in Mowiol (Calbiochem).
Slices were washed in sodium acetate and TBS and mounted.
Hydrochloric acid alcohol was added for 1 minute and then slices were washed for 25 minutes.
Subsequently, the slices were washed twice with Krebs solution, and the protocol was started.
Slices were washed with water and processed for embedding in paraffin.
More suggestions(15)
brain slices were immersed
brain slices were injured
brain slices were embedded
brain slices were pretreated
brain microvessels were washed
brain slices were examined
brain slices were mounted
brain slices were used
brain slices were exposed
brain hemispheres were washed
brain slices were performed
brain slices were verified
brain slices were made
brain slices were put
brain slices were stored
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