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In the case of liquid foams, the main reason is that the resolution of dynamic tomographic microscopy is insufficient to resolve the films between individual cells, yet the analysis imperatively expects each single cell uniquely labeled to distinguish the boundaries between them.
Similar(59)
As is well known, the resolution of fluorescence microscopy(~200 nm) is insufficient to distinguish structural details such as double mitochondrial membrane in mitochondrial division.
We could not investigate this by confocal microscopy, as the resolving power is insufficient.
However, spatial resolution of light microscopy may be insufficient, and scanning electron microscopic images are often subject to artifacts.
In regions were sub-patent recurrences are frequent, evaluation of treatment efficacy based on clinical signs and microscopy might be insufficient and likely underestimate the true number of recurrent infections.
Confocal microscopy identified peripheral immunostaining for RyR (173), but the resolution is insufficient to resolve whether RyR were in the PM or within ER lying close to it.
Howbeit, light microscopy just affords a resolution of 100 200 nm at best, which is insufficient to define clear chromosome conformation.
It is insufficient.
But this is insufficient.
But partial disclosure is insufficient.
Age alone is insufficient.
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CEO of Professional Science Editing for Scientists @ prosciediting.com