OMIP‐095 : 40‐Color spectral flow cytometry delineates all major leukocyte populations in murine lymphoid tissues

• Published in: Cytometry. Part A Vol. 103; no. 11; pp. 839 - 850
• Main Authors: Kare, Aris J., Nichols, Lisa, Zermeno, Ricardo, Raie, Marina N., Tumbale, Spencer K., Ferrara, Katherine W.
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.11.2023
• Subjects: Animal models; Animals; Blood; Blood circulation; Bone marrow; Color; Dendritic cells; Eosinophils; Flow cytometry; Flow Cytometry - methods; Immune system; Immunity, Innate; Immunology; Immunophenotyping; Immunotherapy; Killer Cells, Natural; Leukocyte migration; Leukocytes; Leukocytes (basophilic); Leukocytes (eosinophilic); Leukocytes (neutrophilic); Lymph nodes; Lymphocytes; Lymphocytes B; Lymphocytes T; Lymphoid cells; Lymphoid Tissue; Macrophages; Mice; Monocytes; Natural killer cells; Peyer's patches; Phenotypes; Surface markers; T-Lymphocytes; murine immunophenotyping; primary and secondary lymphoid tissues; cell sorting; innate and adaptive immunity; pre-clinical research; extracellular staining; systems immunology; full spectrum flow cytometry

High‐dimensional immunoprofiling is essential for studying host response to immunotherapy, infection, and disease in murine model systems. However, the difficulty of multiparameter panel design combined with a lack of existing murine tools has prevented the comprehensive study of all major leukocyte...