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WT or Rag1 /– recipient mice (Thy1.2+) were transferred with e.c.
Objectives: To assess the success of in vitro fertilization when embryos were transferred with low or high fluid volume.
Then the chamber was allowed to cool down to room temperature and the GUVs were transferred with a glass pipette to a glass test tube.
At this stage none of the females were LsRV positive (Fig. 5b), hence if viral particles were transferred with the spermatophore, the viral RNA level must have been below the detection limit.
Total protein (50 100 μg) was subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis and the resolved proteins were transferred with EzFastBlot transfer buffer (ATTO) to a polyvinylidene difluoride (PVDF) transfer membrane (ATTO).
To determine whether GMP differentiation to Ly6G+ cells is affected by the intrinsic or extrinsic need for miR-223, we generated BM chimeric mice in which CD45.1+ WT or CD45.1+ miR-223−/+ BM cells were transferred with an equal number of CD45.2+ BM cells into lethally irradiated CD45.2+ recipients.
Liquid reagents were transferred with syringes.
Patients were transferred with a delay of 40 H after burns [H1 H264].
During ConA treatment, control and Treg-depleted mice were transferred with or without BM-MDSCs.
(B) Rat mesenteric artery samples were transferred with platelet samples as controls.
The IMQ (35 mg/day -treated mg/day -treatedferred with PBS, 1 × 106 micer M(IL-23) macrophages.
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