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Once the protein is expressed in live mice, it emits a stable signal that can be observed using two-photon microscopy, indicating the locations of these GFP-labeled synaptic molecules.
Microphase-separated morphology of PCL-b-PAN has been observed by transmission electron microscopy, indicating the formation of self-assembled nanostructure.
The size and its distribution, and formation of metal nanoparticles were confirmed by transmission electron microscopy indicating the diameter of the silver nanoparticles in the range of 3 8 nm.
EGFP-Er, but not EGFP selectively bound to immobilized platelets as detected by confocal microscopy indicating the preservation of Er disintegrin activity and its potential use as a marker for αIIbβ3 integrin.
This is illustrated in (Additional file 1: Figure S1, Inspection of primary-cultured rat ependymal cells by scanning electron microscopy), indicating the validity of primary-cultured rat ependymal cells for this study.
There was no red fluorescence that can be observed on the PLM films, while, in the case of CD133-PE conjugated PLM film, fluorescence tagging of the CD133 antibodies showed uniform distribution on the surface of the polymer film under fluorescence microscopy, indicating the antibodies have been successfully conjugated to the carboxyl groups on the surface of the polymer film.
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Light microscopy indicates the presence of an erosion zone, a distinct area where mass loss occurs.
Transmission electron microscopy indicated the formation of the nanocomposite with 18 24 nm silver nanoparticles and 8 12 nm magnetite nanoparticles.
Fluorescence microscopy indicated the existence of the immobilized enzyme in the hydrogels.
Raman spectroscopy and atomic force microscopy indicated the absence of an appreciable decrease in the MWCNT aspect ratio.
Scanning electron microscopy indicated the different morphologies of injection moulded samples at different locations in the mould.
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