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We also found that the transplanted tissues contained mouse CD31+ cells forming duct-like structures (Fig. 7B), which indicated that transplanted tissue also contained mouse blood vessels.
Based on IHC, most small caliber vessels were lined with human CD31-expressing EC, whereas larger vessels contained mouse CD31+ EC or a combination of human CD31+ and mouse CD31+ EC (data not shown).
Interestingly, all (100 %) of the plaques contained mouse apoE (Fig. 4a, b); whereas only a very small percentage (1.67 ± 1.14 %) of plaques also contained apoE4 (Fig. 4a).
The synovial and myelin microarrays contained mouse and/or human versions of the proteins and peptides, depending on their availability from the collaborators that provided these antigens.
In each staining run, a positive control section was included which contained mouse spinal motor neurons with known mercury deposits from a previous intraperitoneal injection of HgCl2.
Importantly, this analysis allowed us to recover the information about organ homology: co-modules contained mouse and human organs that are known to be homologous.
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One G3 pedigree (Figure 1A) contained mice with very low grip strength (Figure 1B).
This test cage was in the center of a rack of cages all of which contained mice.
At this stage, all the groups contained mice bearing skin papillomas, some of which had progressed to malignancy.
This involved putting known, approved drugs into dishes containing mouse cells infected with abnormal prions.
Mouse neuroblastoma cell line, N1E-115, wastablyly transfected with expression vector containing mouse NeuroD2 cDNA under HSP promoter.
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