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Small explants of each tissue were set up.
(d) Table with the corresponding measured radioactivity of each tissue.
The sections of each tissue were carefully placed on silane-coated slides.
Finally, the μ-values of each tissue type were calculated based on Lambert-Beer's law.
Figure 6 Posterior probability maps of each tissue class (air, soft tissue, and bone) computed from four independent patient datasets.
a Representative images showing H&E staining (left) and PARP1 immunofluorescence staining (right) of each tissue type.
Portions of each tissue sample were flash-frozen in liquid nitrogen or fixed in Zn-formalin.
Total RNA from 1.0 g of each tissue sample was extracted using TRIzol reagent (Invitrogen Corp).
A basic local alignment search tool (BLAST) database was constructed for the ESTs of each tissue.
We sectioned thirty 2-µm thick sections of each tissue sample.
Iodine uptake was normalized dividing the count by the weight of each tissue.
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