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A non-invasive MRI imaging and bone quantification procedure was designed to follow bone regeneration, and these data were extended by μCT imaging and histomorphometry on undecalcified sections for analysis at cellular level.
In order to evaluate the distribution of hMSCs within a brain tumor, tissues were flash frozen and cut into 10 µm sections for analysis.
However, including nonconserved promoter sections for analysis yields many more false positives for TFBSs, thus resulting in more noise in the analysis.
To confirm the presence of the virus in the brains of animals used to prepare infected brain homogenate, some of the animals were processed to obtain ultrathin sections for analysis with a Zeiss EM 900 transmission electron microscope, as described elsewhere [73].
GE cut sections for analysis.
All histological analysis, including selection of sections for analysis, was performed blinded to treatment group.
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After visually identifying assemblage type, 19 sub-sections for analysis were defined by the haphazard placement of a 50×50 cm stainless steel quadrat on top of a mat.
Following fixation the paraffin embedded lungs were sectioned for analysis.
Ten plants of each RNAi line and 5 anthers per plant were paraffin sectioned for analysis.
For standardization, tibial, tarsal and metatarsal bones had to be present in the same section for analysis.
Biopsy samples obtained at arthroscopy were embedded in Tissue Tek medium and then snap-frozen and stored in liquid nitrogen until sectioned for analysis.
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