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Updated: Jan 19, 2026

Isolation of Mouse Kidney-Resident CD8+ T cells for Flow Cytometry Analysis
Published on: June 27, 2020
Multiparametric Flow Cytometry Analysis of Naïve, Memory, and Effector T Cells
Ankit Saxena1, Pradeep K Dagur1, Angélique Biancotto2
1Flow Cytometry Core Facility, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
This study presents a flow cytometry method using a nine-color panel to distinguish between naïve, memory, and effector T cells. This technique is vital for immune response analysis and profiling.
Area of Science:
- Immunology
- Cell Biology
- Biotechnology
Background:
- Polychromatic flow cytometry is key for identifying cell surface markers and defining phenotypes.
- Differentiating T cell subsets (naïve, memory, effector) is crucial for understanding immune responses and profiling.
- Existing methods lack single markers to segregate T cell subsets, necessitating multi-marker approaches.
Purpose of the Study:
- To describe a flow cytometry-based method for characterizing naïve, memory, and effector T cell phenotypes.
- To verify a nine-color panel for T cell subset identification in human donors.
Main Methods:
- Utilized polychromatic flow cytometry.
- Developed and verified a nine-color panel including markers: CD3, CD4, CD8, CD45RO, CD28, CD95, CCR7, Live/Dead Aqua, and a dump channel (CD19, CD14, CD56, CD16).
Main Results:
- Successfully identified six distinct CD4 and CD8 T cell populations.
- The panel effectively distinguished between naïve and effector T cell subsets.
- Demonstrated the utility of a multi-marker panel for comprehensive T cell phenotyping.
Conclusions:
- The validated nine-color flow cytometry panel provides a robust method for dissecting T cell populations.
- This approach aids in detailed immune profiling and understanding immune responses.
- The method is applicable to human samples for immunological research.
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