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Protocol to study the immune profile of syngeneic mouse tumor models.
Miyauchi, Sayuri; Arimoto, Kei-Ichiro; Liu, Mengdan; Zhang, Yue; Zhang, Dong-Er.
  • Miyauchi S; Moores Cancer Center, University of California, San Diego, La Jolla, CA 92037, USA.
  • Arimoto KI; Moores Cancer Center, University of California, San Diego, La Jolla, CA 92037, USA.
  • Liu M; Moores Cancer Center, University of California, San Diego, La Jolla, CA 92037, USA; School of Biological Sciences, University of California, San Diego, La Jolla, CA 92037, USA.
  • Zhang Y; Moores Cancer Center, University of California, San Diego, La Jolla, CA 92037, USA; School of Biological Sciences, University of California, San Diego, La Jolla, CA 92037, USA.
  • Zhang DE; Moores Cancer Center, University of California, San Diego, La Jolla, CA 92037, USA; School of Biological Sciences, University of California, San Diego, La Jolla, CA 92037, USA; Department of Pathology, University of California, San Diego, La Jolla, CA 92037, USA. Electronic address: d7zhang@health.u
STAR Protoc ; 5(3): 103139, 2024 Jun 14.
Article en En | MEDLINE | ID: mdl-38878286
ABSTRACT
Flow cytometry, single-cell RNA sequencing, and other analyses enable us to capture immune profiles of the tumor microenvironment. Here, we present a protocol to characterize the immune profile of tumor-bearing mice. We describe steps for establishing mouse models and preparing single-cell suspensions from tumor tissue and other immune-related organs, which can be further analyzed by flow cytometry and other omics assays. We then detail procedures for staining, flow cytometry analysis, and phenotyping of the immune cell populations. For complete details on the use and execution of this protocol, please refer to Miyauchi et al.1.
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