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LCM-isolated islets from each mouse were processed separately.
Each experimental analysis, 15 20 brain sections per mouse were processed.
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After a 48 hr survival time the mouse was processed according to the procedure described by Hunt and Slotnick [ 5] to determine if any olfactory receptor cell terminals could be detected in remnants of the aspirated olfactory bulb.
End of life (EOL) mice were processed for histochemical analyses.
Six of the nine mice were processed for histopathological examinations.
Three mice were processed in each experimental group.
6 weeks post-operations, femurs from DAP12-/-FcRγ-/ mice were processed for histological examination.
Periovarial WAT from HFD-fed wildtype and HSL null mice were processed in parallel according to the following scheme.
Retinal sections of 12 months old mice were processed for immunohistochemistry using the streptavidin horse radish peroxidase complex.
Optic nerves from transcardially perfused mice were processed for light microscopy of semithin sections as recently reported [1].
A total of 78 culture-positive heart, joint and skin specimens from the 29 infected mice were processed for DNA and analyzed for the bacterial load.
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