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The sections under microscope were photographed at original magnification ×100.
MOG-immunostained sections viewed on an Olympus IX-70 microscope were photographed with a Spot 2 CCD (charge-coupled device) digital camera using Spot Advanced image acquisition software (Diagnostic Instruments).
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Cells were then washed in running tap water to remove the excess stain, air-dried and subjected to microscopic examinations under light microscope and were photographed.
After staining, RSCs were visualized using a fluorescence microscope and were photographed at random per well.
Light-microscope images were photographed, and the total pyramidal cell numbers per millimeter in the hippocampus and in the subregions CA3 were measured on the photographs and then averaged to give a single value.
The stained matrix was assessed using a Nikon Diaphot inverted microscope and samples were photographed using a Nikon 35-mm camera (Nikon, Tokyo, Japan).
Morphological changes of cell nucleus were examined in a fluorescence microscope, and they were photographed using a digital color camera DFC 300 FX (Leica, Wetzlar, Germany).
Cartridges were viewed in the electron microscope and single cartridges were photographed at 11.500× magnification on 80-mm negative film.
Abeta42 immunostained hippocamapal sections from control and lithium-treated animals were observed under a Nikon Eclipse 50i microscope and CA1 plaques were photographed using a 10x objective.
Tissue sections were observed on a Nikon Eclipse E600 microscope and nonoverlapping images were photographed with a Nikon DS-Ri1 digital camera.
Images were photographed with a microscope and camera (DMLB2 microscope and DFC320 camera; Leica, Basel, Switzerland).
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