By FRET microscopy, we have visualized crucial molecular binding events during cell differentiation, signaling flow, growth and/or death13,14,15,16,17,18.
Using single-molecule atomic force microscopy, we have investigated the mechanical properties of bovine tenascin-X in detail.
Using atomic force microscopy we have examined the surface morphology of sequentially biaxially oriented polypropylene (BOPP) films.
Combining steered molecular dynamics simulations, protein engineering and single-molecule atomic force microscopy, we have rationally engineered a bihistidine-based metal chelation site into TNfn3.
Using atomic force microscopy, we have obtained direct three-dimensional visual evidence of the size and shape of native protein-free mineralites isolated from mature bovine bone.
Using fluorescence microscopy we have tracked the cellular binding, surface motion, and internalization of polyarginine and polyethylenimine, cationic ligands used for gene and protein delivery.
Using confocal microscopy, we have assembled an "atlas" of H. diminuta organ architecture that will be a useful resource for helminthologists.
Using atomic force microscopy we have examined morphology of sub-monolayer thick pentacene layers, deposited on exfoliated single-layer and bilayer graphene, transferred onto SiO2.
Using electron microscopy and atom probe field ion microscopy, we have demonstrated that Ag+Si additions produce multi-component clustering reactions.
Using electron microscopy, X-ray, and light microscopy, we have characterized functionalized superparamagnetic iron oxide (SPIO) nanoparticles, and determined their ability for rapid entry and release of the cancer drug doxorubicin in human pancreatic cancer cells.
Using cryo-electron microscopy we have now generated a ∼13 Å three-dimensional map of DNA-PKcs, revealing the overall architecture and topology of the 4128 residue polypeptide chain and allowing location of domains.
