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Number of sponge spicules, phytoliths, pollen including spore, plant fragments, excepting diatom, were counted until a total of 200 pieces were reached under a magnification of 400, using Nikon ECLIPSE 50i POL, and each ratio was calculated.
Cells from 3 different fields were counted under the light microscope under a magnification of ×200.
Following diaminobenzidine development and counterstaining with hematoxylin, the hexon and fiber staining patterns were evaluated under a magnification of × 200.
All the photomicrographs were taken under a magnification of 400×.
The knee joint was examined under a magnification scope.
Positively stained cells were counted in 5 randomly selected fields under a magnification of 400×.
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Fig. 2 FESEM images of the sample Mo9 under a low-magnification b high-magnification and sample MS9 under c low-magnification and d high-magnification.
Cells in the filter were counted under a microscope at a magnification of 20.
d is the same sample of Fig. 4a but viewed under a lower magnification.
Figure 2b,c shows SEM images of the prepared sample under a different magnification factor.
The blood films were stained with a 5% Giemsa for 30 minutes and 100 fields were examined under a 10×100 magnification microscope.
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CEO of Professional Science Editing for Scientists @ prosciediting.com