Exact(3)
Seminiferous tubule diameters were determined using NIS-Elements Basic Research software (Nikon).
The heights of the pillars as well as their diameters were determined using an optical microscope (Keyence VHX-2000D equipped with a VH-Z20R/W lens).
The myotube diameters were determined using a light microscope (Olympus CKX41, with a 20× objective lens; Olympus, Tokyo, Japan) with a digital camera system (Olympus C7070; Olympus, Tokyo, Japan) and MediaCybernetic Image-Pro Plus software (MediaCybernetic, Bethesda, MD, USA).
Similar(57)
Morphology and mean particle diameter were determined using a JEM-2100F microscope (JEOL, Freising, Germany).
BET surface area and average pore diameter were determined using a Micrometrics Tristar II surface area and porosity analyzer.
Surface morphology and MWCNT diameter were determined using high-resolution transmission electron microscopy (HR TEM, JEOL Jem-2100).
A thickness of 3,530 nm and pore sizes ranging from 25 to 45 nm in diameter were determined using scanning electron microscopy (data not shown).
Particle size distribution and mean diameter were determined using an N5 Submicron Particle Size Analyzer (Beckman, USA) [ 18].
Cell concentration, viability and average cell diameter were determined using the Vi-CELL™ XR device (Beckman Coulter).
The grain hardness index and other characteristics, such as weight, moisture, and seed diameter, were determined using the Single Kernel Characterization System in two experiments.
SC and LC nuclear size and seminiferous tubule diameter were determined using an Olympus Optical BH-2 microscope (Olympus Optical Co., Tokyo, Japan) fitted with a Prior automatic stage (Prior Scientific Instruments, Cambridge, UK) and Image-Pro Plus (version 4.5.1) with Stereologer-Pro 5 plug-in software (Media Cybernetics, Bethesda, MD, USA).
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