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Because no clear morphological markers of dedifferentiation are apparent under an inverted microscope, we employed other methods to observe the sequential morphological variation over the course of differentiation at nanometer scale.
The AOD microscope we employed is optimized for fast 2D random-access scanning of neuronal cell populations, as such, its functionality is not being affected by the variation of the FOV.
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We employed MicroScope platform to compute synteny of B. terrae BS001 using data from PkGDB and NCBI RefSeq databases.
We employed "MicroScope" (Vallenet et al. 2013) to predict the presence of RGPs in the BS001 genome.
For image acquisition, we employed a microscope Nikon Eclipse 55i microscope (Nikon, Tokyo, Japan).
To observe these processes in SIP and SLP in even greater detail, we employed a microscope with a super resolution detection system and found bouton-like structures of MBON-α1 attached to the dendrites of PAM-α1.
In this study, we employed transmission electron microscope to observe the ultrastructure of PFC and used PCR and Western blot to measure the expression of related signal molecules.
We employed a Scanning Tunnelling Microscope (STM) to study the surface topography and spatially resolved local electronic properties like local density of states (LDOS) of nanostructured films of La0.7 Sr0.3 MnO3 (LSMO).
These microscope objectives, which we employ for both imaging and focusing of the trapping light, have a much lower numerical aperture (NA) and magnification than typically used for single-beam optical tweezers.
Microscope was employed for investigating the morphological of cells.
To scrutinize the surface morphology of TIPS-pentacene films, an optical microscope was employed.
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