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Twenty-five women and 15 men completed a questionnaire, and provided biologic specimens for quantification of Hg, Pb, Cd, and As using ICP-MS.
Human cortical specimens for quantification of raft-associated γ-secretase activity were obtained from those brains that were removed, processed and placed in −80°C within 12 h postmortem [Patients were placed in a cold (4°C) room within 2 h after death] at the Brain Bank at Tokyo Metropolitan Institute of Gerontology.
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Specimens for miRNA quantification were collected 24 h after the second injection.
The present study showed that CBCT imager, with a spatial resolution as high as 80 μm, had significant correlations with histomorphometry on decalcified bone specimens for ex vivo quantification of peri-implant trabecular microstructure.
To determine viability of sponges affected by long-term actin knockdown, all specimens that were used for quantification in the long-term experiment were time-lapse imaged during the 24-hour period preceding sampling and preparation for RNA quantification.
Furthermore, signal-to-noise ratios are likely not to be sufficient for quantification of specimens of low concentration.
The two remaining specimens referring to PM and GM were used for quantification of yttrium content.
We have developed a proximity assay for quantification of total c-MET expression in FFPE specimens.
For each specimen, two images per region of interest were captured at 20× magnification for quantification.
For each specimen, 40 50 frontal cortex neurons with distinct expression of MAP2 fluorescence and nuclear staining were selected for quantification of RORA and aromatase fluorescence intensities.
For quantification of the total area of ductular reaction (DR), non-overlapping fields of the biopsy specimen were photographed at 100× magnification after immunohistochemical staining for CK7.
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