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In-depth electron microscopy analysis reveals the existence of large strain variations in the grain interior.
The transmission electron microscopy analysis reveals the microstructure of the entangled nano-apatite in the chitosan polymeric matrix.
High resolution transmission electron microscopy analysis reveals that the metal nanoparticles have a high degree of crystallinity.
The subsequent immuno-electron microscopy analysis reveals the three-dimensional (3D) architecture of the same structure, together with the precise identification of the GFP-labeled protein pattern.
Atomic Force Microscopy analysis reveals that a smooth surface can be obtained only in the [580 680] °C growth temperature range for a sufficiently large V/III ratio.
Surface analysis using Auger Nanoprobe Microscopy analysis reveals that a KCN etch can selectively remove potentially harmful Ag-rich secondary phases, therefore improving the MoO3/AZTSe junction quality.
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Moreover, immunofluorescence microscopy analysis revealed induction of type IV collagen by Ring1b- or Suz12-knockdown (Fig. 1I).
The electron microscopy analysis revealed that filamentation (pseudohyphae) was associated with ring and rough colonies.
Transmission electron microscopy analysis revealed that the obtained nanofibers are polycrystalline in nature.
Scanning electron microscopy analysis revealed that bacterial foulants were significant contributors to membrane fouling.
Scanning transmission electron microscopy analysis revealed that the PolyQKd-32 fibrils have 50% higher mass-per-length than PolyQKd-33.
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