<HashMap><database>NODE</database><scores/><additional><omics_type>Genomics</omics_type><submitter>Zhaoyuan Fang</submitter><technology_type>ChIP-Seq</technology_type><full_dataset_link>https://www.biosino.org/node/experiment/detail/OEX00002089</full_dataset_link><experiment_platform>Illumina HiSeq 2000</experiment_platform><experiment_library_layout>Paired</experiment_library_layout><experiment_library_selection>ChIP</experiment_library_selection><experiment_mate_pair>Y</experiment_mate_pair><sample_count>4</sample_count><tissue>['lung']</tissue><taxonomy>['Mus musculus']</taxonomy><experiment_protocol>Cells were cross-linked with 1% formaldehyde for 5 min at room temperature, lysed by SDS Lysis buffer and sonicated to generate DNA fragments with an average size of 500 bp. After pre-clearing with Protein G beads, antibodies against ARID2 (SC 98299X, Santa Cruz), RNA polymerase II (SC 900, Santa Cruz) or control IgG was added to cell lysate and incubated at 4℃ overnight. DNA crosslinked with ARID2 was pulled down with Protein G beads and washed and purified with minelute PCR purification kit (NO. 28004, QIANGEN). Aliquots of ChIP-enriched DNA were subjected to sequencing. Libraries were prepared according to Illumina's instructions for ChIP-seq.</experiment_protocol><repository>NODE</repository></additional><is_claimable>false</is_claimable><name>ChIP-seq</name><description>Arid2 ChIP experiments were performed in K and KL mouse models for sequencing.</description><dates><publication>2021-12-31</publication><submission>2019-11-08</submission></dates><accession>OEX00002089</accession><cross_references><NODE>OEP00000654</NODE></cross_references></HashMap>