Until now, the density of synapses in the human brain could only be determined by autopsy, using antibodies that bind to and stain specific synaptic proteins, or electron microscopy to examine the fine structure of the tissue.
Finally, the fracture surfaces are examined using scanning electron microscopy to examine the crack propagation characteristics.
Here we have used siRNAs and time-lapse epifluorescence microscopy to examine the roles of various candidate mitotic cyclins in chromatin condensation in HeLa cells.
We used cryo-electron microscopy to examine their binding to capsids, whose architecture observes T = 16 icosahedral geometry.
Additional specimens were prepared for transmission electron microscopy to examine the ultrastructure and nanoleakage within the sealer-radicular dentin interface.
By using confocal microscopy to examine the incorporation of fluorescently labeled proteins, spatial control over protein localization was exhibited.
The present study used confocal microscopy to examine cell and nucleus morphology in isolated chondrocytes compressed in alginate constructs.
We used electron backscatter diffraction and transmission electron microscopy to examine the microstructure of the Ti materials.
Whiskers were produced under various conditions, and their features were compared using electron microscopy to examine the growth mechanism.
Here we use high-resolution transmission electron microscopy to examine a sample of Damascus sabre steel from the seventeenth century and find that it contains carbon nanotubes as well as cementite nanowires.
The technique, details of which are published this week in the open-access journal PLOS ONE, looks at the luminescence of different dyes and uses digital microscopy to examine fibres.
