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Figure 4 shows samples of confocal microscope imaging of stained actin fibers among four groups.
In situ transmission electron microscope imaging of microstructure evolution during a temperature cycling from 25 to 500°C was performed to explain changes in tribological properties.
This observation is supported by scanning electron microscope imaging of extracted soot that reveals large soot structures composed of much smaller chains of individual primary particles.
Spontaneous sarcoplasmic reticular (SR) Ca2+release events during metabolic acidification were investigated using confocal microscope imaging of Fluo-4-loaded ventricular myocytes.
Correlative electron microscope imaging of the fluorescent dots, including immunolabeling of coatomer, would theoretically be needed to address this distinction, which is probably semantic in any case since many COPI vesicles have uncoated portions (Faini et al., 2012).
For confocal microscope imaging of intact myocytes, cells were pre-loaded with 10 μ m Fluo-4-AM (20% Pluronic-DMSO) for 30 min followed by a 20 min wash.
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In the top right is a picture taken with our microscope imaging system of a dimpled fiber coupled to a torsional optomechanical device.
The phase retrieval algorithms used are primarily based on the iterative method of Gerchberg and Saxton, which was initially developed for the electron microscope imaging case where two corresponding sets of measurements, the magnitudes of an image and its diffraction pattern, are available.
Figure 2 Diagram of the stereoscopic microscope imaging system.
However, the spatial resolution of the thermal microscope imaging system based on an uncooled infrared detector is low.
With optical micro-scanning technology, the spatial resolution of the thermal microscope imaging system can be increased without increasing the detector dimension or reducing the detector unit size.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com