Abstract
Identification and isolation of senescent cells is challenging, rendering their detailed analysis an unmet need. We describe a precise one-step protocol to fluorescently label senescent cells, for flow cytometry and fluorescence microscopy, implementing a fluorophore-conjugated Sudan Black-B analog, GLF16. Also, a micelle-based approach allows identification of senescent cells in vivo and in vitro, enabling live-cell sorting for downstream analyses and live in vivo tracking. Our protocols are applicable to cellular systems, tissues, or animal models where senescence is present. For complete details on the use and execution of this protocol, please refer to Magkouta et al.
| Original language | English |
|---|---|
| Article number | 102929 |
| Number of pages | 16 |
| Journal | STAR Protocols |
| Volume | 5 |
| Issue number | 1 |
| Early online date | 8 Mar 2024 |
| DOIs | |
| Publication status | Published - 15 Mar 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Animals
- Cell Separation
- Flow Cytometry
- Fluorescent Dyes
- Models, Animal
- Cellular Senescence
- Cell-based Assays
- Molecular/Chemical Probes
- Cell isolation
- Cancer
- Cell Biology
ASJC Scopus subject areas
- General Immunology and Microbiology
- General Biochemistry,Genetics and Molecular Biology
- General Neuroscience
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