Exact(1)
The beam was deflected for scanning by an integrated two-dimensional acousto-optic deflector (Brimrose 2DS-50-30-1.06, www.brimappedconto and mapped onthethe back-aperture of an objective using two concave mirrors that replace the scan lens and the tube lens in a traditional microscope.
Similar(59)
Cuticles were imaged on a Zeiss LSM780 with a 25× objective using a 550 nm laser.
Images of the doublecortin positive cells were obtained under a 40X objective using an Olympus BH-2 microscope with a Panasonic GP-KR222 camera.
Cell somata were identified and counted in both hemispheres, with a 40X objective using an Olympus BX51 light microscope linked to a computer.
To measure wing area, the right forewing was photographed under a 0.3X objective, using a 1X zoom, and a 10X eyepiece.
All sections were photographed on a Nikon Eclipse E600 microscope (Tokyo, Japan) with a 40X objective using a Spot RT camera.
Epifluorescence images were obtained through a 10× objective using a Nikon E800 fluorescence microscope with a Roper Scientific MicroMAX 1024B charge-coupled device (CCD) camera (Princeton Instruments).
Images of the trabecular area were obtained with a 10× objective using an Olympus BH2 microscope (Olympus, Melville, NY).
Photographs of eyes were captured with a 4× objective using a constant exposure and lighting conditions.
Images were acquired by bright field microscopy with a 40X objective using a Nikon Eclipse E800 microscope (Nikon USA, Melville, NY) equipped with a Nikon DXM1200 digital camera.
Images were acquired with a ×20 objective using a Zeiss AxioCam MRc5 microscope in combination with AxioVision 4.8 software.
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