During ConA treatment, control and Treg-depleted mice were transferred with or without BM-MDSCs.
The IMQ (35 mg/day -treated mg/day -treatedferred with PBS, 1 × 106 micer M(IL-23) macrophages.
While maintained in the same position, the mice were transferred to computed tomography (CT) to obtain contrast-enhanced images of the aortic arch.
The PyMT transgenic mice were transferred from the breeding facility at the Wallenberg laboratory to Department of Comparative Medicine, Karolinska Institutet, Sweden, and were acclimated 1 week prior to the first PET and MRI sessions.
The anesthetized mice were transferred from the fDOT to PET scanner by means of the mouse supporting plate, while great care was taken to avoid movement of the animal in regard to its support.
Conventionally raised (CONV-R) Swiss Webster mice were transferred into identical isolators at weaning.
2×105 T regulatory cells per mice were transferred into Foxn1Δ/Δ mice.
Serum from naïve (NS), wP- or wPP-vaccinated mice were transferred to naïve animals.
Dissected uteri from embryonic day 17 pregnant NMRI mice were transferred to ice cold PBS (Gibco).
However, when mice were transferred to a cold environment, the emerging multilocular adipocytes stained positive for COX1 and COX2.
After the scanning, tumors from both groups of mice were transferred to decalcifying solution for 7 days at room temperature.
