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Experiments were performed with laser scanning confocal microscopy at high magnification.
Confocal microscopy at high magnification revealed enzyme uptake by albumin-positive hepatocytes (Figure 7B).
To examine pG12-driven accumulation of EGFP at the cellular level in the midgut epithelia we used fluorescence microscopy at high magnification.
Sections were viewed by bright field microscopy at high magnification under oil immersion.
Specimens were evaluated by microscopy at high power magnification (× 100) in a blinded manner.
To examine how the leader and rear cells behave in embryos, we performed time-lapse live imaging confocal microscopy at high resolution.
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Transmission electron microscopy (TEM) at high magnification of thin cross-sections of drawn multifilament poly (ethylene terephthalate) yarn and of this yarn after heat-setting in the slack state at 250°C and in the taut state at 258°C is shown to provide evidence for the existence of crystallites whose lateral dimensions are consistent with those measured from wide-angle X-ray diffraction (WAXD).
Our microscopy studies at high magnification and high resolution have revealed a clear segregation between Aβ-immunoreactivity and that of APP and its C-terminal fragments (CTFs).
Transmission electron microscopy images at high magnification show a hexagonal lattice structure, and selected area diffraction shows the typical hexagonal spot pattern of h-BN, confirming the high crystalline quality at the microscopic level.
It was difficult to obtain cryo-TEM and conventional transmission electron microscopy images at higher concentrations used for electrospinning experiments (3 wt %) because the large number of nanofibers in solution rendered thick films that were no longer electron-transparent.
Resulting coatings, characterized by transmission electron microscopy (TEM) also at high resolution (HREM), show multilayer structure consisting of sub-layers of W-C H type, W-C Haltypeately high and lowithngsten concentralternately
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