While isolating immune cells from spleens and lungs is routinely achieved using flow cytometry, it is challenging to isolate viable immune cells from skin. Here, we describe a step-by-step protocol for skin digestion using a murine melanoma model, which is amenable for detection of low abundant immune cell populations including group 2 innate lymphoid cells.
Keywords: Cancer; Cell isolation; Flow Cytometry/Mass Cytometry; Immunology; Model Organisms.
© 2021 The Author(s).