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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.
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].
Since progenitor cells from bone marrow were used, it was not clear whether one single chosen reference gene would be expressed.
Similar(54)
A subset of the whole marrow was used to isolate CD34+ cells using EasySep magnetic nanoparticles (StemCell Technologies, Vancouver, Canada).
Bone marrow was used as the source for all transplants.
Normal human bone marrow was used as a control.
When aged marrow was used to replace the marrow in young irradiated mice, tumour metastases decreased.
One mL of bone marrow was used for Cytospin preparation and stained for ICC analysis.
One mL of whole blood/bone marrow sample was used for immunophenotyping studies by flow cytometry and the remaining 3-4 mL of blood/bone marrow was used for separation of PBMC using Histopaque-1077 Sigmaion (Sigma, USA) for genetic studies.
More suggestions(15)
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marrow were isolated
marrow were harvested
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marrow were incubated
marrow were estimated
marrow were exposed
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marrow were derived
marrow were selected
marrow were purified
marrow were evaluated
marrow was used
marrow were examined
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