That way, particle inception, growth by coagulation and rapid coalescence, followed by agglomeration at the later process stages was visualized.
GFP fluorescence in the different blood stages was visualized and recorded using the GFP filter settings of a Leica TCSSP2 laser scanning confocal microscope.
Liver-stages were visualized by measuring luciferase activity of parasites (expressing luciferase under the eef1a promoter) in whole bodies of mice (Ploemen et al., 2009).
Late S-phase stage nuclei [39] were visualized for clarity of replicating foci colocalization, or lack thereof.
Atomic manipulation was used to control the reductive rearrangement of 1,1-dibromo alkenes to acetylenes on a NaCl surface at 5 K, and the stages of the reaction were visualized with atomic resolution using AFM.
Highly developed filopodia and lamellipodia were visualized at early cell spreading stage in K716A mutant cells.
Mice were killed at different stages of pregnancy, and the whole placenta and fetus were visualized under a fluorescence stereomicroscope.
GV spreads were prepared from stage VI oocytes and the chromosome axis and the lateral loops were visualized using DAPI.
Sections were visualized using a BX-50 microscope (Olympus) fitted with a motorized specimen stage and microcator.
