Protocol for intranuclear Nrf2 detection in activated mouse, human, and Jurkat T cells by spectral flow cytometry
Nuclear factor erythroid 2-related factor 2 (Nrf2) coordinates cellular antioxidation responses. Its expression increases in T cells upon activation. Here, we present a protocol for quantitative detection of intranuclear Nrf2 in activated mouse, human, and Jurkat T cells using spectral flow cytometry. We describe procedures for primary T cell isolation, in vitro activation, intranuclear staining, and flow cytometric acquisition and analysis, including gating strategies for CD4<sup>+</sup> and CD8<sup>+</sup> T cells. For complete details on the use and execution of this protocol, please refer to Tripathi et al.<sup>1</sup>.
Authors
- Aprajita Tripathi
- Debolina Dasgupta (ORCID: https://orcid.org/0000-0002-4953-8026)
- Kalyani Pyaram (ORCID: https://orcid.org/0000-0003-2744-7470)
- Nadine Santana-Magal (ORCID: https://orcid.org/0000-0001-9834-4634)
- Gabrielle Fisette
- Mehak Ahuja
Institutions
- The University of Kansas Cancer Center (US)
- University of Kansas Medical Center (US)
Publication Details
- Journal
- STAR Protocols
- Published
- 2026-02-11
- DOI
- https://doi.org/10.1016/j.xpro.2026.104360
- Primary Topic
- Genomics, phytochemicals, and oxidative stress
- Type
- article
- Field-Weighted Citation Impact
- 0.00