<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Guohong Li</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0017199000</full_dataset_link><submitter_email>liguohong@whu.edu.cn</submitter_email><submitter_affiliation>Wuhan University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>FLAG-IP–MS profiling of SPINDOC interactome using a HeLa–Tet-On–FLAG-SPINDOC-GFP cell line</name><description>HeLa–Tet-On–FLAG-SPINDOC-GFP cells were established for inducible expression and affinity purification. FLAG-SPINDOC-GFP expression was first induced by doxycycline treatment. Subsequently, cells were either left unsynchronized or arrested at the G2/M phase by nocodazole treatment. Efficient expression and enrichment of FLAG-SPINDOC-GFP were confirmed by FLAG co-immunoprecipitation. Immunoprecipitates were then subjected to mass spectrometry analysis to identify SPINDOC-associated proteins, particularly under mitotic conditions.</description><dates><publication>Fri May 15 00:00:00 BST 2026</publication></dates><accession>PXD078443</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>