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Epifluorescence microscopy of samples undergoing indentation and subsequent video image correlation analysis allowed determination of strain maps.
The bulk structure of PVA hydrogels was investigated by scanning electron microscopy of samples prepared by freeze-etching.
The crystallographic features of surface α precipitates accompanied by surface tilt(s) in a Ti 5.26 wt.% Cr alloy have been comprehensively studied by transmission electron microscopy of samples prepared using a focused ion beam.
Atomic force microscopy of samples was observed on a Multimode 8 (Bruker/USA).
However 20% of TgPrP S3.F88W) mice had areas of apparently normal fibre morphology lying adjacent to fields of hypermyelinated fibres (Fig 4A), with transmission electron microscopy of samples from the same animals also revealing normally myelinated fibres lying adjacent to hypermyelinated fibres.
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The resulting PrPSc fibrillar aggregates were analyzed by electron microscopy of sample aliquots and quantified.
The images of atomic force microscopy (AFM) of samples were obtained by using a Bruker Dimension Icon microscope VT-1000 System operated in tapping mode.
With the relatively intensity of D band to the G band (ID/IG) and the transmission electron microscopy images of samples, we obtain that the optimum synthetic temperature is about 900 °C.
STM and transmission electron microscopy observations of samples on HOPG and CB indicated that the prepared catalysts were highly dispersed at the atomic level.
Figure S2: (a and b) Polarized microscopy images of samples prepared at 1 and 10°C/min, respectively.
Similar results were obtained by fluorescence microscopy (CoM) of samples stained with Proteostat, a red fluorescent aggregate sensing dye (Usmani et al., 2014).
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