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For normalization of the densitometric measurements, the unspecific background staining of the brain sections was measured at cortical areas where no BrdU+ or Tbr1+ cells depending on the kind of immunostaining were detectable.
The geometric imperfection of the fabricated sections was measured.
The quantity of CM-Dil-labeled double positive cells in the immunofluorescence staining sections was measured under a Nikon TE2000-S microscope.
The p53-dependent apoptosis related Bax proteins on formalin-fixed paraffin-embedded sections were stained by the avidin-biotin peroxidase complex method The apoptosis incidence in the sections was measured by hematoxylin-eosin staining.
The crypt length in the HE sections was measured (in ≥8 crypts per field) as the distance from the base to the apical side.
For egg chamber staging, the length of mid sagittal sections was measured according to Spradling (1993).
Similar(38)
At least 10 measurements were made for each section, and eight sections were measured in each animal.
Three sections were measured for each mouse.
Differential cross sections are measured and well described by the theoretical predictions.
Velocity profiles at the inlet and exit sections are measured with hot-wire anemometer.
A two-dimensional profile of the deposit across the channel at selected axial sections is measured.
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