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Serial coronal sections were made at 50 µm on a freezing microtome and all brain sections were collected.
Briefly, rat brain sections were collected and rinsed in PBS and incubated in blocking solution (rat: 2% bovine serum albumin, 0.2% Tween-20 in PBS; mouse; M.O.M. kit, Vector Laboratories, Burlingame, CA, USA) for 2 hours at room temperature (RT).
Brain sections were collected and stained as described above.
Brain sections were collected onto two slide sets of eight slides per set.
The brain sections were collected in a 50% glycerol solution and kept at −20°C.
Cryostat brain sections were collected from animals killed at 48 h of recovery.
Similar(52)
To rule out the confounding effects of an occult leukemia, glioma or pheochromocytoma, a complete blood count, lymph node sampling, spleen biopsy, sternum bone marrow, adrenal gland biopsy and whole-brain sections were collected and examined histologically.
Fresh frozen coronal, 30- μm-thick cryostat brain serial sections were collected from −1.3 to −2.2 bregma (total thickness of the examined tissue was 1500 μm).
The VTA was dissected according to the Mouse Brain Atlas [28] and sections were collected from 1.68 mm to −2.12 mm relative to bregma.
OCT preserved brains were cryosectioned and 10 μm sections were collected from the Bregma +1.0 location.
Alternate 20-µm thick coronal sections were collected from each brain from the rostral to the caudal end of the SCN or DMH (24 32 total, 12 16 for each probe) by using a Leica CM3050S cryostat.
More suggestions(15)
brain scans were collected
brain sections were placed
brain waves were collected
brain images were collected
brain resections were collected
brain sections were incubated
brain volumes were collected
brain sections were deparaffinized
brain sections were stored
brain sections were processed
brain sections were stained
brain regions were collected
brain sections were coverslipped
brain sections were used
brain sections were exposed
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