Sentence examples for brain sections were taken from inspiring English sources

For staining to be quantifiable and comparable, 4 brain sections were taken from positions 0.26, −0.46 −1.18 and −1.94 mm relative to bregma [36], from every mouse (n = 6 7), in all 8 groups and all 192 sections stained concurrently for each marker and developed for exactly the same period of time.

The brain sections were taken from the hypothalamus (−0.40 and −3.60 mm from the bregma) [47], washed in 0.01 M PBS (Sigma) for GnRH and CRH experiments or in Tris-buffered saline (50 mM Tris, 0.9% NaCl, pH 7.5) for AR experiments; the endogenous peroxidase and nonspecific binding were removed by incubation with 3% H2O2 for 30 min and 0.5% Triton X-100 10 min at room temperature.

After freezing, 50 μm coronal brain sections were taken and mounted throughout the rostral-caudal extent of the nucleus accumbens.

For the analysis of cortifugal axon development, images of labeled rat brain sections were taken on a Zeiss AxioImager M1 microscope using a 40× 0.75 numerical aperture (NA) objective.

On gestational day 20, rats were perfused, brains were dissected, and cryostat sections were taken, labeled in vitro, and placed on Hyperfilm for 4 weeks.

For RMS analysis, 4 equivalent representative sections were taken from each brain and immunostained for pHH3 and Dcx.

Serial 6 μm frozen sections were taken from microvessel-rich brain samples.

Serial 4-μm sections were taken through the entire head (for analysis of the brain) or thorax (for indirect flight muscle analysis).

The brains were then frozen and 50 µm coronal sections were taken.

Representative sections were taken from multiple areas of the brain and all other organs.

Coronal 20µm-thick frozen sections were taken at 400µm intervals spanning the brain from frontal to striate cortex.