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An ANOVA model was used to compare mean optical density among different exposure durations.
The mean optical density of the COMT hybridization signal on X-ray film was significantly higher in the gray matter than in the white matter area in both diagnostic groups (Figures 1b and 2).
To determine fiber density in the striatum, the mean optical density (O.D).
Background subtraction was performed using the mean optical density value from 4 arbitrarily selected, vessel-free, areas (60×60 pixels).
The mean optical density of each spot was normalized to the positive control and compared between control and treated epithelia (Fig. 2C).
Graphed data are presented as the mean optical density (group means mGluR5/actin immunolevels) ± the standard error of the mean (SEM).
and the mean optical density (M.O.D).
The mean optical density of antigen-stimulated cultures/mean optical density of medium-only cultures was determined for each culture treatment and recorded.
Proliferation rates (PRs) were calculated using the following formula: PR = mean optical density at day 7 mean optical density at day 1.
Mean optical density values of Day 0 plates were subtracted from those of sample plates.
The cut-off value equaled 0.2 plus the mean optical density (OD) of negative controls.
More suggestions(16)
represent optical density
mean optical technology
mean optical signal
mean microvascular density
mean vascular density
mean optical cavity
mean faunal density
mean optical transmittance
mean optical background
mean optical power
mean pneumococcal density
mean dry density
mean fluorescent density
mean optical zone
mean optical path
mean optical flow
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