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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM413994"><item key="CELL TYPE">Lower-SP HSC</item></item></item><item><item key="GSM413994"><item key="CELL TYPE">Lower-SP HSC</item></item></item><item><item key="GSM413994"><item key="CELL TYPE">Lower-SP HSC</item></item></item><item><item key="GSM413997"><item key="CELL TYPE">Upper-SP HSC</item></item></item><item><item key="GSM413997"><item key="CELL TYPE">Upper-SP HSC</item></item></item><item><item key="GSM413997"><item key="CELL TYPE">Upper-SP HSC</item></item></item></item><item key="id">5714</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">The traditional view of hematopoiesis has been that all the cells of the peripheral blood are the progeny of a unitary homogeneous pool...</item><item key="geo_gse_id">E-GEOD-16475</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">6</item><item key="tags"><item>hematopoietic system</item><item>peripheral</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">expression-data-from-side-population-subfraction-h</item><item key="geo_id_plat">E-GEOD-16475_A-AFFY-45</item><item key="name">Expression data from side population subfraction hematopoietic stem cells</item><item key="created">Nov.11, 2014</item><item key="summary">The traditional view of hematopoiesis has been that all the cells of the peripheral blood are the progeny of a unitary homogeneous pool of hematopoietic stem cells (HSCs).  Recent evidence suggests that the hematopoietic system is actually maintained by a consortium of HSC subtypes with distinct functional characteristics.  We show here that myeloid-biased HSCs (My-HSCs) and lymphoid-biased (Ly-HSCs) can be purified according to their capacity for Hoechst dye efflux in combination with canonical HSC markers. We used microarray expression profiling to determine the transcriptional profiles of myeloid-biased lower-SP HSCs and lymphoid-biased upper-SP HSCs Three biological replicates were analyzed for each HSC subpopulation.  Lower-SP and upper-SP HSCs were purified from three pools of mice on separate days.  HSCs were further purified with the addition of canonical HSC makers; Sca-1+ c-Kit+ Lineage-</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-16475</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-16475/samples/</item></data></biogps>
