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<biogps><data><item key="platform">4</item><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSE10070GSM254523"><item key="phenotype">monolayer control</item></item></item><item><item key="GSE10070GSM254523"><item key="phenotype">monolayer control</item></item></item><item><item key="GSE10070GSM254523"><item key="phenotype">monolayer control</item></item></item><item><item key="GSE10070GSM254538"><item key="phenotype">low transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254538"><item key="phenotype">low transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254538"><item key="phenotype">low transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254615"><item key="phenotype">mid transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254615"><item key="phenotype">mid transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254615"><item key="phenotype">mid transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254618"><item key="phenotype">plateau transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254618"><item key="phenotype">plateau transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254618"><item key="phenotype">plateau transepithelial electrical resistance</item></item></item><item><item key="GSE10070GSM254618"><item key="phenotype">plateau transepithelial electrical resistance</item></item></item></item><item key="id">2722</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-10070</item><item key="summary_wrapped">To further understand the differences occurring in MCF10A cells as they polarize and differentiate in the Transwell&#174; model, we performed...</item><item key="pubmed_id">19005683</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">13</item><item key="tags"><item>genome</item><item>point</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">gene-expression-in-mcf10a-cells-through-differenti</item><item key="geo_id_plat">E-GEOD-10070_A-AFFY-44</item><item key="name">Gene Expression in MCF10A cells through Differentiation on Transwells</item><item key="created">Aug.12, 2014</item><item key="summary">To further understand the differences occurring in MCF10A cells as they polarize and differentiate in the Transwell&#174; model, we performed gene expression profiling with Affymetrix Human Genome U133 Plus 2.0 Arrays.  Four experimental time points, were sampled:  conventional cultures of MCF10A cells grown on plastic (Monolayer) and MCF10A cells plated on Transwells&#174; sampled at three TEER values, 200-300 &#937; cm2 (Base), 1400-1600 &#937; cm2 (Midpoint), and 3000-3200 &#937; cm2 (Plateau).  Experiment Overall Design: Cells are grown in monolayer to 90-95% confluency, trypsinized and counted for seeding onto permeable supports (Transwell&#174;, 0.4 &#181;m pores, polyester) in normal growth medium.  MCF10A cells are seeded on 12-well Transwells&#174; (Corning) at 105 cells/cm2.  Both chambers of media were changed strictly on a 24-hour schedule.  Transepithelial electrical resistance (TEER) is measured daily with Epithelial Volt-Ohm Meter (EVOM; World Precision Instruments), prior to media change.  Total RNA was isolated at the indicated TEER listed above.  Canonical monolayer MCF10A cells served as a control comparison.  Each time point was performed on triplicate arrays except for Plateau (n=4).</item><item key="geo_gse_id">E-GEOD-10070</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-10070/samples/</item></data></biogps>
