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Results were compared with reference control mice processed in the same fashion.
To see how the mice processed these smell signals, the researchers turned to the brain's smell center, the olfactory cortex.
This staining pattern was not detected in cardiac tissue sections from dt mice processed in parallel (Fig. 1).
Macrophages from DR1-tg mice processed intact hCII for presentation of the glycosylated epitope hCII259 274 to T-cell hybridomas.
However, spinal cord sections from Plp1tg mice processed alongside the EAE sections showed non-specific staining, mainly in axons.
Lungs, kidneys, spleens, hearts, intestines and livers were obtained from scurfy and WT mice; processed according to standard laboratory procedures; and stained with H&E.
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The mouse processes 12,000 frames a second at 5,001 CPI – I'm assuming that's some high-end stuff there.
Spleens from 3 month-old MRL/ lpr γ3 +/+, +/-, and -/- mice and C3H control mice were processed into single-cell suspensions for analysis by flow cytometry.
In brief, fourth (abdominal) mouse mammary fat pads from FVB mice were processed by mechanical and enzymatic dissociation to liberate single cells.
End of life (EOL) mice were processed for histochemical analyses.
Six of the nine mice were processed for histopathological examinations.
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