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Exact(15)
Random fields per coverslips at 63x magnification were captured using Leica confocal microscope (Leica TCS SP2, Wetzlar, Germany).
Field of interest were chosen and images (at x40 magnification) were captured for 24 h for both groups (mature and immature consortia) using autofocus property.
The fluorescence and bright field photographs of cells at 10× magnification were captured 24 h post infection (p.i).
Five images (×40 magnification) were captured at each level.
Ten to fifteen random fields (× 100 magnification) were captured for each membrane.
Images of three random fields (10× magnification) were captured from each membrane, and the number of migratory cells was counted.
Similar(45)
Images with each zoom magnification are captured, and the Spot diagram and MTF are simulated using Zemax software.
An image of the fibers at 100 time magnification was captured in a dry state.
One image/spot at 200X magnification was captured from each specimen in human tissue microarrays.
The medium was replaced with 2 % Matrigel every 3 to 4 days and microscopic images (200x magnifications) were captured at 2 day intervals for 2 to 3 weeks.
Images of the PAS stained sections (1,000× magnifications) were captured using Axioskop 2 for each liver from four control and four HgCl2-treated fishes.
More suggestions(15)
magnification were shown
magnification were scored
magnification were kept
magnification were recorded
magnification were digitized
magnification were observed
magnification were used
magnification were taken
magnification were photographed
magnification were examined
magnification were determined
magnification were performed
magnification were counted
magnification were analyzed
magnification was captured
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