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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="GSE1776GSM30759"><item key="growth condition">control</item></item></item><item><item key="GSE1776GSM30759"><item key="growth condition">control</item></item></item><item><item key="GSE1776GSM30759"><item key="growth condition">control</item></item></item><item><item key="GSE1776GSM30759"><item key="growth condition">control</item></item></item><item><item key="GSE1776GSM30774"><item key="growth condition">starved</item></item></item><item><item key="GSE1776GSM30774"><item key="growth condition">starved</item></item></item><item><item key="GSE1776GSM30774"><item key="growth condition">starved</item></item></item></item><item key="id">8435</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">8</item><item key="summary_wrapped">C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal...</item><item key="pubmed_id">15608089</item><item key="geo_gse_id">E-GEOD-1776</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">7</item><item key="tags"><item>serum</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-by-array-of-mouse-myotubes</item><item key="geo_id_plat">E-GEOD-1776_A-AFFY-36</item><item key="name">Transcription profiling by array of mouse myotubes grown under control and starvation conditions</item><item key="created">Nov.24, 2014</item><item key="summary">C2C12 mouse myoblasts (American Type Culture Collection, Manassas, VA) were maintained in growth medium (DMEM supplemented with 10% Fetal Bovine serum, Invitrogen Corporation, Carlsbad, CA) in 5% CO2. Cells were plated at a density of 40-50% in 100mm dishes. When cells reached ~90% confluency 24 hours later, they were switched to differentiation media (DMEM containing 2% horse serum; GIBCO, Invitrogen Corporation, Carlsbad, CA) which was subsequently changed every 48 hours. All cells were allowed to differentiate for 4 days with feeding every two days (day 0, 2, and 4). Beginning at day 4, control cells were re-fed every 48 hours whereas experimental cells were not re-fed. After an additional 4 days (8 days post differentiation), cells were harvested and total RNA was isolated from control and starved (non re-fed cells)</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-1776</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-1776/samples/</item></data></biogps>
