ApoE isoforms differentially alter baseline antioxidant levels critical to ferroptosis mitigation

ABSTRACT: U87 cells overexpressing ApoE isoforms were treated with sulforaphane for 18 hours for comparison with a DMSO control. ApoEChimp is on the ApoE4 backbone but contains R61T which is thought to be the isoform defining residue.

INSTRUMENT(S): Illumina NovaSeq 6000

ORGANISM(S): Homo sapiens

SUBMITTER: Max Thorwald 

PROVIDER: E-MTAB-16242 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress