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Plaques were then counted using a plate microscope.
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Plaques were counted with a plate microscope.
Viral plaques were counted with a plate microscope.
Use a plate.
Use a plate or a paper towel.
The labeling solution was removed and the plates washed twice, and we then counted the tubes in the plate using a fluorescent microscope.
It is based on the direct observation of a thin metallic sample embedded between polished glass plates using a light microscope.
Sporulation cultures were digested with Zymolyase 20T in sorbitol buffer and tetrads were dissected on YPD plates using a dissection microscope; 10 cells of freshly dissected spores were allowed to grow for 24 hr in YPD media at 30°.
(c) MDA-MB-231 cells transiently expressing MYO10-mCherry were plated on FN, stained for active Src (pSrcY416) and imaged using a TIRF microscope (scale bar, 20 μm).
(a,b) MDA-MB-231 cells transiently expressing MYO10-mCherry were plated on FN, stained for active integrin (12G10 clone) (a) or talin-1 (b) and imaged using a TIRF microscope (scale bar, 20 μm).
Colonies were fixed with 6.0% glutaraldehyde, stained with 0.5% crystal violet, and counted using a dissecting microscope to determinate plating efficiency (PE).
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