NIH3T3 cells showing the localization of nuclear transport factor RanBP1 and F-actin in interphase cells. Cells were fixed in formaldehyde and labeled with a primary antibody to RanBP1 and Cy3-conjug...

NIH 3T3 cell transfected with EGFP-VASP. VASP is localized to the focal adhesions and is also present along the protruding leading edge. VASP only hightlights the portions of the periphery that are ...

Confocal microscope image of a 3T3 fibroblast cell. The nucleus has been stained blue, and two components of the cytoskeleton, actin microfilaments and intermediate filaments, are stained red and gree...

NIH 3T3 cell (mouse embryonic fibroblast line) stained for Actin (green) and DNA (blue). PLoS Biology February 2009|Volume 7|Issue 2| e1000038 Active-Site Inhibitors of mTOR Target Rapamycin-Resist...

The f-actin staining in the lamella of a cultured fibroblast shows common features of adherent cells on a flat substrate. The dominant f-actin organization is in the form of stress fibers, linear bun...

Confocal micrograph of NIH-3T3 cells co-transduced with 5 fluorescent proteins. The cells were marked by co-transduction with Lentiviral Gene Ontology (LeGO) vectors expressing Cerulean (cyan), EGFP ...

To study the molecular mechanism by which nonmuscle myosin II (MII) regulates protrusion and adhesion dynamics in migrating cells, NIH3T3 cells were treated with scrambled siRNA (Scr) for 2 days, trea...

To study the molecular mechanism by which nonmuscle myosin II (MII) regulates protrusion and adhesion dynamics in migrating cells, NIH3T3 cells were treated with βPIX-specific siRNA for 2 days, treat...

NIH 3T3 cell expressing EGFP-Lifeact (a small genetically expressed probe that binds to actin and is derived from the first 17 aa of Abp140) imaged with structured illumination. Structured illuminati...

To study the molecular mechanism by which nonmuscle myosin II (MII) regulates protrusion and adhesion dynamics in migrating cells, NIH3T3 cells were treated with βPIX siRNA for 2 days, treated with b...