They first examined placentas from mice at various stages of pregnancy, isolating RNA from both the maternal and fetal components of this lifeline.
Fig. 9 Representative H&E stained images of major immune organs including the liver, spleen and kidney collected from AMP-QDs treated mice and control mice at various time points via intravenous injection.
We obtained over 500 immunoglobulin G1 clones harboring VH186.2 from the spleen, bone marrow, and microdissected individual germinal centers of (4-hydroxy-3-nitrophenyl) acetyl-immunized C57BL/6 mice at various time points postimmunization.
However, even modified YopD, YopO and YscF antigens were only able to partially protect immunized mice at various levels against lethal challenge with Y. pestis KIM 1001 strain while no protection was observed with either the YopB or Pla antigens.
The clinical scores of Olig1−/− EAE mice at various time points were summarized in Figure 1C.
For validation studies using ELISA, we collected plasma from infected mice at various stages of tumor progression and controls.
These results prompted us to analyse the expression of SRF in skeletal muscles isolated from control mice at various ages.
To examine whether GFP+ dentate granule cells also show similar developmental changes, we imaged GFP+ cells in GAD67-GFP BAC transgenic mice at various developmental stages.
Labelling was initiated by the intravenous injection (into the vein of the tail) of 4-OHT into pregnant mice at various times after coitus.
To test p53 tumor suppressor functions in a novel experimental context, we somatically deleted both p53 alleles in multiple tissues of mice at various ages.
The responses of GC levels and storage cell numbers in Vela- and Imig-treated Gaucher mice at various doses provide a backdrop for clinical applications and decisions.
