Using genetic tag visualization by electron microscopy, we reveal the molecular organization of ten human eIF3 subunits, including an octameric core.
By careful electrochemical exposure along with high-resolution electron microscopy, we reveal that microstructural features down to a few nanometers in size can behave as unique electrochemical entities.
Combining crystallography, nuclear magnetic resonance, and electron microscopy, we reveal the structure of the Bcl10 CARD filament and the mode of interaction between CARMA1 and Bcl10.
By confocal microscopy analysis we revealed a higher co-localization degree (Pearson coefficient, r = 0.96) between Drp1 and TOMM20 in 3T3-L1 adipocytes upon NR (Fig 3D) and increased mitochondrial fission was also observed in starved X9 adipocytes (Fig 3B).
As the strength of our system is live-tracking of cell cycle progression, we performed video microscopy, which revealed both CMs' divisions (Suppl. Video 2) as well as binucleation (Suppl. Videos 3 + 4) taking place.
Microscopy observation revealed spindle-shape cell morphology.
Fluorescent microscopy revealed a dramatic increase in punctate structures, considered reflective of autophagosome formation, which we quantified by counting.
Electron microscopy revealed their neuronal morphology.
Scanning electron microscopy revealed minimal endothelial denudation.
Scanning electron microscopy revealed the bowl-shaped nanoparticles.
Subsequent fractography by scanning electron microscopy revealed distinct failure mechanisms.
