<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Jeroen Pennings</submitter><funding>Horizon Europe Research and Innovation Programme</funding><funding>European Union’s Horizon 2020 Research and Innovation Programme</funding><species>Homo sapiens (human)</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-BSST2296</full_dataset_link><repository>biostudies-other</repository><funding_grant_id>101057014</funding_grant_id><funding_grant_id>964537</funding_grant_id><pubmed_authors>Jeroen Pennings</pubmed_authors></additional><is_claimable>false</is_claimable><name>Malondialdehyde formation in HepG2 cells after compound exposure</name><description>We quantified malondialdehyde formation in maturated HepG2 cells after 24 h of compound exposure. This was done using three exposure scenarios: (1) cells receiving acute exposure; (2) cells receiving repeated exposure; (3) cells receiving repeated exposure and recovery. Lipid peroxidation was assessed by measuring malondialdehyde (MDA) levels using the thiobarbituric acid reactive substances (TBARS) assay [Wong et al. Clin Chem. 1987;33(2 Pt1):214-20]. Fluorescence was measured in the supernatant at λexc= 530 nm and λem= 575 nm using a 96-wells fluorescence plate reader. The MDA levels were quantified using a standard curve.
This study was performed as part of the RISK-HUNT3R project and the PARC project.</description><dates><release>2026-03-31T00:00:00Z</release><modification>2026-06-29T04:01:37.936Z</modification><creation>2025-11-20T12:23:14.493Z</creation></dates><accession>S-BSST2296</accession><cross_references/></HashMap>