Applications that fall into this category are holographic microscopy; particle-size analysis; high-speed photography of various types, particularly of gas flows; data storage and retrieval, including displays; image formation through a random medium; and non-optical holography, particularly acoustic holography.
Our results are interpreted in the context of the results of others that were obtained using cryo-electron microscopy (and single particle analysis), negative staining and freeze fracture electron microscopy, as well as previous AFM studies.
We further obtain a three-dimensional structure of both native and recombinant CSN using electron microscopy and single particle analysis.
Structural analysis by electron microscopy and single particle analysis revealed that dimer formation is based on specific interaction of the F0 parts, not the F1 headpieces which are not at all in close proximity.
In cryo-electron microscopy and single particle analysis, data acquisition and image processing are generally carried out in sequential steps and computation of a three-dimensional reconstruction only begins once all the micrographs have been acquired.
The effects of matrix modification and organoclay structure on the morphology and properties of these nanocomposites were evaluated using stress strain analysis, wide-angle X-ray scattering (WAXS), and transmission electron microscopy coupled with particle analysis.
Electron microscopy and laser particle analysis acknowledge that yttria addition aids powder agglomeration during ball milling.
Over the last five years, thanks to the development of direct detection devices (DDDs) (Milazzo et al. 2005), cryo-electron microscopy (cryoEM) single particle analysis (SPA) has transitioned from being an established, but limited, technique to being at the forefront of structural biology (Eisenstein 2016; Nogales 2016).
The fine structure of the capsid envelope, which has been well characterized both with atomic force microscopy and single particle analysis on virions whose fiber coatings were removed, suggests a p3 symmetry of depressions with the capsomers being arranged in a p6 symmetry [11, 12].
To compare hDmc1-ssDNA complexes formed in the presence of ATP and Ca2+ with the RecA/RadA/Rad51 family nucleoprotein filaments we employed electron microscopy and single particle analysis.
