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CyTOF supports efficient detection of immune cell subsets from small samples.
Yao, Yi; Liu, Rebecca; Shin, Min Sun; Trentalange, Mark; Allore, Heather; Nassar, Ala; Kang, Insoo; Pober, Jordan S; Montgomery, Ruth R.
Afiliação
  • Yao Y; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
  • Liu R; Department of Immunobiology, Yale University School of Medicine, New Haven, CT, United States.
  • Shin MS; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
  • Trentalange M; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
  • Allore H; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
  • Nassar A; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
  • Kang I; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
  • Pober JS; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States; Department of Immunobiology, Yale University School of Medicine, New Haven, CT, United States; Human and Translational Immunology Program, Yale University School of Medicine, New Haven, CT, United Stat
  • Montgomery RR; Department of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States; Human and Translational Immunology Program, Yale University School of Medicine, New Haven, CT, United States. Electronic address: ruth.montgomery@yale.edu.
J Immunol Methods ; 415: 1-5, 2014 Dec 15.
Article em En | MEDLINE | ID: mdl-25450003
ABSTRACT
Analysis of immune cell states is paramount to our understanding of the pathogenesis of a broad range of human diseases. Immunologists rely on fluorescence cytometry for cellular analysis, and while detection of 8 markers is now well established, the overlap of fluorescent signals limits efficiency. Mass cytometry or CyTOF (Cytometry by Time-Of-Flight) is a new technology for multiparameter single cell analysis that overcomes many limitations of fluorescence-based flow cytometry and can routinely detect as many as 40 markers per sample. This technology provides tremendous detail for cellular analysis of multiple cell populations simultaneously and is a powerful technique for translational investigations. Here we present reproducible detection of immune cell subsets starting with as few as 10,000 cells. Our study provides methods to employ CyTOF for small samples, which is especially relevant for investigation of limited patient biopsies in translational and clinical research.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pele / Células Dendríticas / Linfócitos B / Células Matadoras Naturais / Monócitos / Linfócitos T Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pele / Células Dendríticas / Linfócitos B / Células Matadoras Naturais / Monócitos / Linfócitos T Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: J Immunol Methods Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos