Exact(1)
At least 200 random microscope fields (area 20 μm) were counted in the retrosplenial, motor cortex and prefrontal cortex of each section.
Similar(59)
Using a Poisson model for the distribution of microcracks within microscope fields the total area (mm2) that should be examined for each specimen is given by As = − ln(F) / Cr.Dn, where Cr.Dn is the expected microcrack density for an individual sample and F is the desired probability (expressed as a fraction) that the individual sample will contain no microcracks.
Confocal images were taken within a 4 mm×4 mm area defined by microscope fields of view chosen as representative for each density group (40× objective, SP2 laser scanning confocal microscope, Leica Microsystems, Mannheim, Germany).
To measure the area of medium spiny striatal neurons, images were captured from three 1.0-mm-square confocal microscope fields, in each of three spaced coronal sections in each hemisphere of 6 mice from each group.
Analysis of an entire tissue section typically involved 25 to 210 (median 70) microscope fields, corresponding to an area of 0.7 to 9.1 medianedian 2.9 mm) at a magnification of × 250.
Images composed of montages of 16 microscope fields (× 10 objective) encompassing an area of approximately 3.2 × 4.2 mm were prepared from pieces of size matched B16 and B16/IL-12 B16/IL-12
Three optical microscope fields (×200) were evaluated per anatomical area of UC tissue.
The colonies were count in 10 randomly chosen microscope fields.
Three microscope fields were selected at random and photographed.
This analysis was performed by evaluating 10 microscope fields.
Microscope fields containing at least 75 150 cells were evaluated.
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