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Subunits of IF were very difficult to image by standard cryo-electron microscopy because of their length and anisotropic shape.
We believe that flow cytometry using DNA stains [32], [38] is preferable to pLDH because of greater sensitivity [34] and to microscopy because of the capacity to evaluate greater numbers of infected erythrocytes with no observer bias.
Myriad fluorescent organic compounds have been employed in fluorescence spectroscopy and microscopy because of their synthetic tunability, bright emission, and wide availability.
The Tetraselmis-type chloroplasts were often discernible within the cytoplasm of R. viridis by light microscopy because of their intraplastidial eyespots.
Decalcification is not recommended for nasal tissues to be examined by transmission electron microscopy because of the detrimental effect of decalcifying solutions on sensory cells.
(29) In these cells, the fluorescent protein was undetectable by fluorescence microscopy because of rapid degradation by the proteasome under steady-state conditions, but detectable in the presence of proteasome inhibitors.
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This is convenient for applications involving fluorescence microscopy, because vesicles of several microns are ideal for imaging, as the optical resolution limit is ∼0.25 to 0.5 µm for conventional microscopes.
This is a critical limitation for photon-limited applications, like single-molecule fluorescence microscopy, because the loss of photons is directly related to a reduction in precision and resolution [ 16, 26].
In addition, the nanorod-shaped Li V O compounds in the galvanostatically cycled samples could not be observed using high-resolution scanning electron microscopy (HRSEM) because of their structural instability, which can be attributed to the deterioration of their electrochemical properties during cycling.
Then, asODN remained outside the cell, as TIRF and fluorescent microscopy showed, because of its poor interaction with PAMAM-OH and cell membranes.
There also exist some highly dispersed Au and Pd monometallic particles that cannot be detected by XRD and transmission electron microscopy (TEM) because of their small particle sizes.
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