Your English writing platform
Discover LudwigSuggestions(5)
Exact(60)
The stained cells were observed on an inverted fluorescent microscope, as described above.
The real-time imaging for caspase activation was evaluated using microscope as described in the 'Materials and Methods'.
Morphological analysis and quantification of neurite bearing cells were performed using phase-contrast microscope as described previously12.
In addition, observations were taken on the number of nematodes in the rhizosphere for each N. benthamiana plant under a microscope as described previously14,61.
The aberration fit routine includes all tertiary Zernike modes and assumes optical parameters for each microscope as described in the Supplementary Methods.
The tilting range was set by the configuration of our microscope, as described later.
Colocalization of PLP2-TM-V5 (red) and eGFP-LC3B (green) were observed using a confocal microscope as described in Fig. 1B.
The cells were fixed at 48 h post-transfection and were analyzed for eGFP-LC3B positive autophagosome accumulation (green) using a confocal microscope as described in Fig. 1B.
For imaging, an inverted microscope (as described above) was used.
The samples were imaged in the electron microscope as described above.
Images were visualized and collected on a Zeiss Axioplan II fluorescent microscope as described previously [29].
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com