Nuclear size was measured by the dark nuclear zone of pom1-tomato fluorescence.
Nuclear size and shape are derived from the average behavior of nuclear features, following segmentation, from a subset of images.
Nuclear size was calculated by measuring the diameter of the nucleus of each cell for all fields, relative to nuclear size in the absence of EPO.
(E) The nuclear size of Rab10 −/− embryos was smaller.
These features include nuclear size, shape, and structure.
Corrected nuclear data (including nuclear size, location, shape) are then stored in data files.
Even today, nuclear morphology measures include nuclear size, shape, DNA content (ploidy) and 'chromatin organization'.
These cells exhibited reduced nuclear size, intense fluorescence, chromatin condensation, and nuclear fragmentation, were considered apoptotic cells.
Untreated 3T3BXB-ER cells also have a slight decrease in nuclear size compared to 3T3 cells.
Cells expressing RNAi against any of these genes had reduced cell and nuclear size and increased punctate LysoTracker phenotype.
Briefly, nuclear size, morphology and cell density measurements are made on nuclei automatically identified in fluorescence channel 1.
