Localization of cross-linking proteins in fibroblast cytoskeleton. Immuno-EM of the cell edge or interior (CIL 34928) of cytochalasin D-treated Xenopus fibroblasts stained with p21 (Arp2/3) primary a
pSIM imaging of the dynamic of the myosin-driven movement of phalloidin-labeled actin filament Raw microscope image from conventional microscope GE DeltaVision OMX SR, SIM reconstruction result via th
Electron micrograph of keratocyte or fibroblast lamellipodial actin network after unprotected extraction. All examples demonstrate frequent branching of actin filaments. Image corresponds to a singl
Localization of Arp2/3 complex at actin filament branching points. Xenopus keratocytes and fibroblasts were treated with CD (0.2 μM for 30 min or 0.5 μM for 10 min), extracted in the presence of phall
Multiple branching of actin filaments in lamellipodia of vertebrate fibroblasts. This image shows a local enlargement of the leading edge shown in overview in CIL 24788. Image corresponds to Figure 1
