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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="id">6402</item><item key="factors"><item><item key="GSM688700 1"/></item><item><item key="GSM688701 1"/></item><item><item key="GSM688702 1"/></item><item><item key="GSM688703 1"/></item><item><item key="GSM688704 1"/></item><item><item key="GSM688705 1"/></item><item><item key="GSM688706 1"/></item><item><item key="GSM688707 1"/></item><item><item key="GSM688708 1"/></item><item><item key="GSM688709 1"/></item><item><item key="GSM688710 1"/></item><item><item key="GSM688711 1"/></item><item><item key="GSM688712 1"/></item><item><item key="GSM688713 1"/></item><item><item key="GSM688714 1"/></item><item><item key="GSM688715 1"/></item></item><item key="pop_total">0</item><item key="platform">6</item><item key="summary_wrapped">c-Myc is one of key players that are crucially involved in maintaining the undifferentiated state and the self-renewal of ESCs. To...</item><item key="pubmed_id">21726832</item><item key="geo_gse_id">E-GEOD-27881</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">16</item><item key="tags"><item>protein</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">effect-of-ablation-of-max-gene-expression-on-es-ce</item><item key="geo_id_plat">E-GEOD-27881_A-AFFY-45</item><item key="name">Effect of ablation of Max gene expression on ES cells cultured under conventional or 2i/Nam condition.</item><item key="created">Nov.11, 2014</item><item key="summary">c-Myc is one of key players that are crucially involved in maintaining the undifferentiated state and the self-renewal of ESCs. To understand the mechanism by which c-Myc helps preserve these prominent characteristics of ESCs, we generated null-ES cells for the Max gene, which encodes the best characterized partner protein for all Myc family proteins. Although Myc/Max complexes have been widely regarded as crucial regulators of the ESC status, our data reveal that ESCs do not absolutely require these complexes in so-called ground state or related conditons and that this requirement is restricted to conventional ES culture conditions without using a MAPK inhibitor. Simply Dox-treated or Nanog (WT or D67G mutant)-rescued Max-null ESCs which were cultured under conventional culture condition and 2i/Nam-treated completely Max-null ES cells from which Dox-regulatable cDNA was removed were used for RNA source. Samples from Dox-untreated Max-null ESCs cultured under conventional culture condition were used as reference samples for Dox-treated cells and Nanog-rescued cells, while a sample from wild-type ESCs cultured under 2i/Nam condition was used as a reference sample for completely Max-null ES cells cultured with 2i/Nam.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27881</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-27881/samples/</item></data></biogps>
