Only intact cells, as identified by forward and side light scatter, were analyzed.
Microbeam grazing incidence small-angle X-ray scattering measurements, which are analyzed with a unified fit model, reveal information about the titania structure sizes.
The sources are collimated on the sample, and the energy spectra of the alpha particles and protons scattered from the sample are analyzed (the proton analysis is implemented only in some spectrometers).
The second is the genome-wide approach, where the pattern of molecular evolution of hundreds to thousands of genes scattered across the genome are analyzed simultaneously (e.g. [ 9- 14]).
The importance and interaction between various factors, including ship main characteristics, operational profile based on a mission or loading condition, wave climatic data represented by the use of different scatter diagrams, wave spectra, heading distributions, are analyzed.
The diffraction spectra of imaginary-part photonic crystal (IPPC) slabs are analyzed using the scattering-matrix method.
At least 104 cells per appropriate lymphocyte or monocyte gate, respectively, according to forward scatter vs side scatter properties were analyzed using a dual-laser cytometer with Cell Quest Pro (FACSCalibur, Becton Dickinson, Heidelberg, Germany and Summitt 4.3 (Beckman Coulter, Krefeld, Germany) software.
In the present study the scatter data was analyzed regionally, revealing that while all regions of aged rabbit lenses had significantly greater scatter than the corresponding regions in adult lenses, the age-related difference was somewhat greater in the region corresponding to the inner cortical fibers.
These cells were collected, stained with CD11c-PE, a cell surface marker of murine dendritic cells and at least 10,000 cells, based on forward and 90° light scatter properties, were analyzed by flow cytometry.
Following incubation, the cells were collected, washed and stained for cell surface markers (CD3,CD4) followed by intracellular cytokine staining (IFNγ, IL-4) and at least 50,000 live cells, based on forward and 90° light scatter properties, were analyzed by flow cytometry as described above.
