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To quantify the turbidity of liquid cultures was used optical density (OD) measured at 600 nm, which was used as a corresponding measure of cell density.
For this reason we used optical density analysis of digitalized images from brain sections that were processed for DAB immunocytochemistry [34], [36].
Both of these predictions were verified in experiments in which we used optical density measurements to follow growth of single-strain cultures (Figure 4).
We used optical density measurements at 600 nm to assess the concentration of bacteria, and confirmed colony forming units (CFU) by plating serial dilutions on MacConkey's agar.
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We used optical densities to progressively lower the incident flux, thus giving access to a 4-order magnitude dynamic range of optical power.
The discovery that bacterial morphology was altered by exposure to DFMO caused us to reexamine our investigations using optical density, as such measurements could be dependent on bacterial size and shape.
The growth of microalgae was mainly monitored by using optical density method.
The relative potency amongst the test compounds was assigned using optical density measurement at 600 nm.
They were scanned using [18F]FEOBV PET, then sacrificed, and their brain tissues collected for immunostaining and quantification of cholinergic denervation using optical density (OD).
Therefore, the results are in good agreement with the values calculated using optical density (OD) at 600 [nm] (see Table1) and with those found in the literature (Corpe1964).
0, 1, 2, 3, 4, 5, 6, 8, 10 and 12 h after the inoculation, the growth of bacteria was monitored using optical density (O.D) method at 600 nm.
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