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The growth and differentiation of individual cell types was determined using live cell fluorescent microscopy demonstrating the utility of fluorescent labels to monitor tissue organization in real time.
Sixteen randomly targeted proteins of diverse functions, fused to the eGFP were identified and analyzed in living cells by epifluorescence microscopy, demonstrating the suitability of the novel tool for massive, random production of fluorescent proteins and for following of these proteins with different localizations inside the prokaryotic cell.
Finally, the interaction of the nanoparticles with breast cancer cells was studied utilizing fluorescence microscopy, demonstrating the potential of the nanoparticles to act as near-infrared fluorescence optical imaging agents and drug-delivery carriers.
Figure 1F (RFOS 2) is high-power microscopy demonstrating the chondroid tissue adjacent to the tumor bone.
For example, classic electron microscopy demonstrating the three types of cell junction of the intercalated disc as spatially discrete structures implies corresponding spatially discrete sites for connexins and adhesion molecules.
The variation in fluorescence signal over the DNA molecule corresponds well with that obtained by confocal microscopy, demonstrating the viability of STED for imaging single DNA molecules and a future potential use for comparison of signal variations caused by sequence specific dye binding or partial melting.
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Scanning electron microscopy demonstrated the development of intercellular gaps.
Atomic force microscopy demonstrated the perfect uniformity and planarity of the cured films.
Furthermore, atomic force microscopy demonstrated the formation of PLLA nanobrushes on the pSi surface.
Immunofluorescent confocal microscopy demonstrated the recombinant TAT-fusion proteins with a mixed endosomal and lysosomal localization.
Immunofluorescence microscopy demonstrated the re-appearance of FSHR expression with increasing days in culture.
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