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One might argue that in three biopsies no tetracycline labels were observed.
Fluorescent labels were observed using antibodies against C/EBPβ, RSKPhosphoSer380, α-SMA, PCNA (Santa Cruz Biotechnology, Santa Cruz, California), active caspase 3 (PharMingen, San Diego, California) or C/EBPβ-PhosphoThr217 [10] in a laser confocal microscope [5][10][42].
Similar(58)
A dipolar interaction between the nitroxide labels is observed in some of the samples.
No differences in COX-2 labeling were observed between the +K and E animals.
Osteoid and fluorescence labeling were observed in the allograft by the 4th and 6th weeks, respectively, but not at any time in the HA.
Similar changes in occludin labeling were observed in cells with NMMIIB and NMMIIC knock-downs (Figure 9, arrows).
No major changes in the size or density of the vesicles following FITC labelling were observed.
With respect to the number of enolase labelled cells, at least 50% cytoplasmic labeling was observed in all cases.
No labelling was observed in interdigitating cells.
In contrast, no cell labeling was observed using 89Zr HPO4 2.
Label was observed in all samples from lesions between 3 8 days after label administration.
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