| Literature DB >> 32926371 |
Ryosuke Nakagawa1, Jason Brayer2, Nicole Restrepo1, James J Mulé1,3, Adam W Mailloux4.
Abstract
The field of flow cytometry has witnessed rapid technological advancements in the last few decades. While the founding principles of fluorescent detection on cells (or particles) within a uniform fluid stream remains largely unchanged, the availability more sensitive cytometers with the ability to multiplex more and more florescent signals has resulted in very complex high-order assays. This results in the co-use of fluorophores with increased levels of emission overlap and/or spillover spreading than in years past and thus requires careful and well thought out planning for flow cytometry assay development. As an example, we present the development of a large 18-color (20 parameter) flow cytometry assay designed to take an in depth analysis of effector lymphocyte phenotypes, with careful attention to assay controls and panel design.Entities:
Keywords: Adaptive immune cells; Immune checkpoint; Innate immune cells; Memory markers; NK cell; NK receptor; NKT cell; T cell
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Year: 2021 PMID: 32926371 PMCID: PMC7744271 DOI: 10.1007/978-1-0716-0849-4_14
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745