<HashMap><database>NODE</database><scores/><additional><omics_type>Genomics</omics_type><submitter>Zengwei Tang</submitter><technology_type>ChIP-Seq</technology_type><full_dataset_link>https://www.biosino.org/node/experiment/detail/OEX00020408</full_dataset_link><experiment_platform>Illumina NovaSeq 6000</experiment_platform><experiment_library_layout>Paired</experiment_library_layout><experiment_library_selection>ChIP</experiment_library_selection><sample_count>1</sample_count><tissue>['human Intrahepatic Cholangiocarcarcinoma Cell Line']</tissue><taxonomy>['Homo sapiens']</taxonomy><experiment_protocol>HuCCT1 cells were cultured in RPMI-1640 medium (Thermo Fisher Scientific, USA) supplemented with 10% fetal bovine serum (FBS) (Thermo Fisher Scientific, USA), 100μg/ml streptomycin (Cienry, Huzhou, CN), and 100 U/mL penicillin (Cienry, Huzhou, CN) at 37 °C in 5% CO2 atmosphere</experiment_protocol><repository>NODE</repository></additional><is_claimable>false</is_claimable><name>OEX_Zengwei_2208181103</name><description>Approximately 1×107 HuCCT1 cells  in the logarithmic phase were fixed with 4% paraformaldehyde and incubated with glycine at 37°C for 10 min. After lysis, shearing of the chromatin into 100-600bp fragments by sonication, the lysates were immunoprecipitated with magnetic protein G beads conjugated with anti-MLF1 antibody or used as Input (positive control).</description><dates><publication>2022-08-18</publication><submission>2022-08-18</submission></dates><accession>OEX00020408</accession><cross_references><NODE>OEP00003577</NODE></cross_references></HashMap>