Exact(2)
After 12 days culture, colony number and morphology was counted using inverted microscope.
The number of cells with nuclear apoptotic morphology was counted in five fields of 100 cells.
Similar(58)
For analysis of activated microglia, IBA-1+ cells that displayed an activated morphology were counted in the same images using ImageJ software (National Institutes of Health).
Emerging clones with undifferentiated morphology were counted and examined for eGFP expression.
Cells with blast and promyelocyte morphology were counted as primitive; those with myelocyte/metamyelocyte morphology as intermediate myeloid; those with band, segmented neutrophil, monocyte, and macrophage morphology as mature myeloid; those with intermediate hemoglobinization as intermediate erythroid; and those with full hemoglobinization as mature erythroid.
Only cells with a monocytoid/macrophage-like morphology were counted.
Only neurons with a clearly visible nuclear morphology were counted.
For brightfield immunohistochemistry, only MAP2-positive cells with unambiguous neuronal morphology were counted as neurons.
However, only those that appear mature in their morphology are counted.
After four days, wells containing cells with hematopoietic morphology were counted.
IL-21+ cells with lymphocytic morphology were counted by eye within predefined areas of each perivascular cuff, and their densities were expressed per mm.
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