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Morphology was imaged by optical microscopy.
The cell morphology was imaged and assessed via quantification of circularity.
Moreover, their surface morphology was imaged by atomic force microscopy and scanning electron microscopy.
Macrophages were grown on flat, 10-, 50-, 100-, and 200-nm nanodot arrays for 3 days, and their morphology was imaged by scanning electron microscopy.
The crosslinked networks and the linear polymers were fluorescently labeled, and the resulting morphology was imaged with confocal fluorescence microscopy and two-photon laser scanning microscopy.
In the corresponding control experiment at 15 mmHg in which only caspase-3/7 and cell morphology was imaged, the MR- DEVD 2 fluorescence intensity reveals that at this pressure the caspase-3/7 level in the RGC-5 cells does not increase indicating the lack of apoptosis.
Similar(51)
Calcium carbonate minerals and biofilm morphology were imaged in PAO1-gfp.
Texture and grain morphology were imaged using a TESCAN Vega2 scanning electron microscope (SEM).
Proximal and distal aortic areas with normal vessel morphology were imaged and showed no overall increase in diameter (data not shown).
Intensity of fluorescence was described in arbitrary units (AU) covering a range from 0 to 60 000 AU. Ca2+ levels and cell morphology were imaged every 10 min for 2 h using an Argon/UV laser (excitation 488 nm/emission 520 nm).
The morphologies were imaged using scanning electron microscopy (SEM) and transmission electron microscopy (TEM).
More suggestions(15)
morphology was described
morphology was determined
morphology was studied
morphology was verified
morphology was analyzed
morphology was inspected
morphology was characterized
morphology was observed
morphology was seen
morphology was measured
morphology was shown
morphology was evaluated
morphology was preserved
morphology was examined
morphology was formed
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