By comparing high-throughput light scattering results with high-resolution electron microscopy (EM), we established that light scattering can efficiently map nanosheet yield and size as a function of time and ion concentration.
Using confocal laser scanning microscopy on live cells, we established and validated fluorescent markers for chloroplasts, Golgi dictyosomes, mitochondria and peroxisomes in moss.
By using scanning electron microscopy (SEM) and infrared data, we established and verified a two-dimensional finite-element model conforming to the size of the practical device to study high-electron-mobility transistors (HEMTs).
In addition, to measure chromatin relaxation at rare positions within the genome, we established live cell microscopy at the GSI microbeam thus allowing the aimed irradiation of small nuclear structures like the Xi.
Here, we established a transmission electron microscopy (TEM) approach to localize gold-labeled DSB repair components in different chromatin environments within the intact nuclear architecture of cells in irradiated mouse tissues.
Here, we establish by immunoelectron microscopy that PLEKHA7 is localized at the AJ belt in epithelial cells.
Here, we carried out all-atom molecular dynamics simulations to map the free-energy landscape of these lattices, validated this landscape through extensive structural characterization by electron microscopy and established that it is predominantly governed by solvent reorganization entropy.
In order to screen a large variety of 1,3,5-benzenetrisamide derivatives with respect to their nucleating potential an efficient and reliable test based on polarized light microscopy was established.
Lens nuclei were Vibratome-sectioned, fixed and prepared for transmission electron microscopy using established techniques.
However, laboratory experiments in 1993 that utilized advanced technology in the field of electron microscopy have established conclusively that the rostrum of American paddlefish is covered with tens of thousands of sensory receptors.
