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Bone marrow was used as the source for all transplants.
Normal human bone marrow was used as a control.
One mL of bone marrow was used for Cytospin preparation and stained for ICC analysis.
In addition, histologically normal bone marrow was used as a positive control in immunostaining for SCF and wound tissue for VEGFR-2.
During sample processing, the left femur containing both bone and the bone marrow was used en bloc since it was difficult to accurately weigh them.
In the second set only CD45.1 donor bone marrow was used, and 17 mice were generated that expressed a GFP control, 19 that received cells that expressed wild type mTRF2, and 17 that were transduced with cells expressing the GFP-mTRF2 fusion.
Similar(53)
TNCs, Lin- or Lin+ cells from human umbilical cord blood or human bone marrow were used for our xenograft studies.
Animals transplanted with wild-type bone marrow were used as control group.
Since progenitor cells from bone marrow were used, it was not clear whether one single chosen reference gene would be expressed.
A FFPE block of N2C-Tpo cells, a Tpo-dependent megakaryocytic leukemia cell line, and of normal bone marrow were used as positive controls for TPO-R expression.
From the patients analyzed, immunocytology screened tumour free peripheral blood cells or frozen bone marrow, were used as normal tissue counterparts [ 16].
More suggestions(16)
bone graft was used
bone marrow was harvested
bone marrow was diagnosed
bone wax was used
bone marrow was perfused
bone marrow was hypocellular
bone marrow was injected
bone marrow was flushed
bone marrow was extracted
bone impaction was used
bone gauge was used
bone marrow was extruded
bone marrow was observed
bone marrow was infused
bone marrow was allowed
bone material was used
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