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OMIP‐007: Phenotypic analysis of human natural killer cells

OMIP‐007: Phenotypic analysis of human natural killer cells Purpose and Appropriate Sample Types This panel was developed to characterize the phenotype of human natural killer (NK) cells from cryopreserved peripheral blood mononuclear cells (PBMC) isolated from ACD or EDTA anticoagulated whole blood or apheresis units (Table 1 ). The application of this panel was to identify changes in NK cell subsets with regard to receptor expression, maturation, homing potential, and activation in the setting of primary HIV‐1 natural infection. However, this panel may be applied to a wide variety of disease and normal conditions to characterize NK cells in humans. The performance of this panel was tested on fresh and frozen PBMC as well as using a whole blood lyse no wash procedure. 1 Summary table for OMIP‐007 Purpose Characterize the phenotype, maturation, and activation of NK cells Species Human Cell types Fresh and cryopreserved PBMC Cross references None Background NK cells are innate effector cells representing ∼10% of circulating lymphocytes with more than 2 billion in circulation at any given time ( 1 ). NK cells are classically defined by the expression of two cellular markers; CD56, the neural cell adhesion molecule (NCAM) and CD16, the Fcγ‐receptor IIIa. These markers (CD56/CD16) allow the discrimination of http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Cytometry Part A Wiley

OMIP‐007: Phenotypic analysis of human natural killer cells

Cytometry Part A , Volume 81A (6) – Jun 1, 2012

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References (9)

Publisher
Wiley
Copyright
Copyright © 2012 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1552-4922
eISSN
1552-4930
DOI
10.1002/cyto.a.22033
pmid
22411905
Publisher site
See Article on Publisher Site

Abstract

Purpose and Appropriate Sample Types This panel was developed to characterize the phenotype of human natural killer (NK) cells from cryopreserved peripheral blood mononuclear cells (PBMC) isolated from ACD or EDTA anticoagulated whole blood or apheresis units (Table 1 ). The application of this panel was to identify changes in NK cell subsets with regard to receptor expression, maturation, homing potential, and activation in the setting of primary HIV‐1 natural infection. However, this panel may be applied to a wide variety of disease and normal conditions to characterize NK cells in humans. The performance of this panel was tested on fresh and frozen PBMC as well as using a whole blood lyse no wash procedure. 1 Summary table for OMIP‐007 Purpose Characterize the phenotype, maturation, and activation of NK cells Species Human Cell types Fresh and cryopreserved PBMC Cross references None Background NK cells are innate effector cells representing ∼10% of circulating lymphocytes with more than 2 billion in circulation at any given time ( 1 ). NK cells are classically defined by the expression of two cellular markers; CD56, the neural cell adhesion molecule (NCAM) and CD16, the Fcγ‐receptor IIIa. These markers (CD56/CD16) allow the discrimination of

Journal

Cytometry Part AWiley

Published: Jun 1, 2012

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