The baseline that was observed in the original study eight
days after inoculation (~ 2 × 106 bioluminescence) was not observed until day 27 post-inoculation in the pilot study.
Eight
days after inoculation mice were injected intraperitoneally (IP) with 75 mg / kg of D - luciferin in 150 μl PBS and imaged 15 min later under isoflurane anesthesia in a Xenogen IVIS Spectrum.
The mice developed neurologic dysfunction between 380 and 660
days after inoculation.
Extracts from the brains of FFI patients transmitted disease to transgenic mice expressing a chimeric human - mouse PrP gene about 200
days after inoculation and induced formation of the 19 - kilodalton PrPSc fragment, whereas extracts from the brains of familial and sporadic Creutzfeldt - Jakob disease patients produced the 21 - kilodalton PrPSc fragment in these mice.
The downy mildew appeared on plants in the dark six
days after inoculation, while no symptoms showed up on the plants that were under the red lights, Patel said.
Following exposure to sheep prions, all rabbits with the sheep PRNP transgene in addition to the full complement of rabbit genes (including rabbit PRNP) developed typical TSE after 6 - 8 months, whereas rabbits without the sheep PRNP transgene remained healthy more than 700
days after inoculation.
Not exact matches
(C) Bioluminescent images of representative mice at
day 22
after inoculation.
(L) Bioluminescent images of bone metastases from representative mice at
day 18
after inoculation.
(C to F) Bioluminescent images (C and E) of bone metastasis from representative mice at
day 22
after inoculation with 1833 cells (n = 10 mice per group) or
day 35
after inoculation with SCP28 cells (n = 8 mice per group).
After rabies
inoculation (an interval of 30
days is suggested), the microchip - identified animal is subjected