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Semi-thin sections of 0.3µm were obtaining, colored in 1% toluidine blue, and evaluated with light microscope combined with image analyzing system.
Three animals of the control group were further evaluated with light microscopy.
Fourth passage cells were used for stimulation experiments and consisted of more than 95% FLSs as evaluated with light microscopy.
Cells were allowed to grow for 8 days, fixed with 1% neutral buffered formalin, rinsed with 70% ethanol, stained with toluidine blue, coverslipped and evaluated with light microscopy.
The Infiltration of Inflammatory cells in the liver tissues was evaluated with light microscopy by senior pathologist at Beijing Union Medical College Hospital [ 5].
Two sham animals were further evaluated with light microscopy and did not show the basal vacuolization at the inner hair cells.
Similar(53)
Protoplast disintegration was evaluated with a light microscope.
CISH results were evaluated with the light microscope at low-power and high-power magnification.
The slides were evaluated with a light microscope at ×400 magnification.
Brain damage after HCA was evaluated with the light microscopy and electron microscopy.
Sections were counterstained with hematoxylin, cover-slipped with DePex (Serva, Heidelberg, Germany), and evaluated with the light microscope.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com