On the day of the experiment, the mice were transported to the imaging facility at least 1 h prior to the experiment.
Before testing, mice were transported into the behavioral room to adapt to the environment for at least 1 hr.
All mice were transported to the behavioral testing room in their home cages at least 1 h before testing.
The presumptive source of virus introduction was contact between wild mice and colony mice, and the outbreak spread among facilities when mice were transported for use as breeding stock.
For blood sampling, mice were transported individually in their home cage to an adjacent laboratory (in order not to disturb circadian rhythm of the mice, the hallway and rooms were under red light conditions).
Immediately prior to testing, mice were transported in their home cage on a cart down a 30 m hallway to a laboratory testing room with standard white fluorescent lighting, and placed individually in a test chamber (light intensity 550 650 lux; sound intensity 65 70 decibels measured within chamber).
When administered intraperitoneally in mice, recombinant CLSP was transported across the blood-cerebrospinal fluid (CSF -barrier and its CSF -barriern in the CSF reandes 1/100 of its serum concentration at 1 h after injecthen.
Hammarstrom, based on elegant autoradiographic studies of C-ascorbate distribution in mice, first proposed that AA was transported into CSF, and then brain, via the CP [ 6, 17, 18].
With a click of the mouse, we are transported to the seaports of Bremen or Liverpool, where giant shipping lines like Cunard, White Star and Hamburg-Amerika herd waiting immigrants into dockside hotels to be examined, fumigated and then quarantined for the trip to New York.
