| Literature DB >> 32421215 |
Amy Fox1, Taru S Dutt1, Burton Karger1, Andrés Obregón-Henao1, G Brooke Anderson2, Marcela Henao-Tamayo1.
Abstract
Flow cytometry allows the visualization of physical, functional, and/or biological properties of cells including antigens, cytokines, size, and complexity. With increasingly large flow cytometry panels able to analyze up to 50 parameters, there is a need to standardize flow cytometry protocols to achieve high-quality data that can be input into analysis algorithms. Without this clean data, algorithms may incorrectly categorize the cell populations present in the samples. In this protocol, we outline a comprehensive methodology to prepare samples for polychromatic flow cytometry. The use of multiple washing steps and rigorous controls creates high-quality data with good separation between cell populations. Experimental data acquired using this protocol can be analyzed via computational algorithms that perform end-to-end analysis.Entities:
Keywords: controls; flow cytometry; high-dimensional flow cytometry data; high-quality data; immunology; phenotyping; sample preparation
Mesh:
Year: 2020 PMID: 32421215 PMCID: PMC8801208 DOI: 10.1002/cpcy.74
Source DB: PubMed Journal: Curr Protoc Cytom ISSN: 1934-9297