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Microscopy confirmed that larvae consumed labelled necrotic epithelial cell contents.
SEM and optical microscopy confirmed that dense deposits were created.
Phylogenetic inquiry and microscopy confirmed that diatoms and an associated aerobic bacterial community facilitated early colonization.
Confocal laser microscopy confirmed that the expression of DsRed2-mito gene exhibited a characteristic punctuate pattern of staining (Fig. 2a).
Atomic force microscopy confirmed that the SiO2 surface roughness increased with increasing CDT processing time (Figure 3).
Scanning electron microscopy confirmed that the gypsum microstructure varied when citric acid is used.
Scanning electron microscopy confirmed that the resultant nanofibers had a linear morphology, smooth surface, and tri-layered structure.
Moreover, morphological studies by scanning electron microscopy confirmed that better adhesion between the uniaxial fabric and the matrix was achieved.
The study by transmission electron microscopy confirmed that the Fe3O4 nanoparticles were closely bonded over CNT surfaces.
Scan-electronic microscopy confirmed that spheroplasts of P. pastoris CL2 cells were bigger (~10 µm diameter) than the control cells (~3 µm diameter).
Transmission electron microscopy confirmed that the epitaxial deposits were initially in a state of relatively high tensile strain.
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