scholarly journals A Single 9-Colour Flow Cytometric Method to Characterise Major Leukocyte Populations in the Rat: Validation in a Model of LPS-Induced Pulmonary Inflammation

PLoS ONE ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. e0142520 ◽  
Author(s):  
Ashton Barnett-Vanes ◽  
Anna Sharrock ◽  
Mark A. Birrell ◽  
Sara Rankin
Keyword(s):  
Pulmonary Inflammation ◽  
Flow Cytometric Method ◽  
Flow Cytometric ◽  
Colour Flow ◽  
Leukocyte Populations

An eight-colour flow cytometric method for the detection of reference values of lymphocyte subsets in selected healthy donors

2013 ◽  
Vol 14 (3) ◽  
pp. 249-259 ◽  
Author(s):  
Bianca Rovati ◽  
Sara Mariucci ◽  
Rossella Poma ◽  
Carmine Tinelli ◽  
Sara Delfanti ◽  
...  
Keyword(s):  
Reference Values ◽  
Lymphocyte Subsets ◽  
Flow Cytometric Method ◽  
Flow Cytometric ◽  
Colour Flow ◽  
Healthy Donors

Three-colour flow cytometric method to measure antibody-dependent tumour cell killing by cytotoxicity and phagocytosis

2007 ◽  
Vol 323 (2) ◽  
pp. 160-171 ◽  
Author(s):  
Marguerite Bracher ◽  
Hannah J. Gould ◽  
Brian J. Sutton ◽  
David Dombrowicz ◽  
Sophia N. Karagiannis
Keyword(s):  
Tumour Cell ◽  
Cell Killing ◽  
Flow Cytometric Method ◽  
Flow Cytometric ◽  
Colour Flow

A sensitive flow cytometric method for measuring the oxidative burst

1997 ◽  
Vol 202 (2) ◽  
pp. 105-111 ◽  
Author(s):  
Michael A Model ◽  
Mark A KuKuruga ◽  
Robert F Todd
Keyword(s):  
Oxidative Burst ◽  
Flow Cytometric Method ◽  
Flow Cytometric

scholarly journals Flow cytometric method for the routine follow‐up of red cell populations after bone marrow transplantation

1997 ◽  
Vol 97 (1) ◽  
pp. 141-145 ◽  
Author(s):  
E. C. M. Hendriks ◽  
A. J. M. De Man ◽  
Y. C. M. Van Berkel ◽  
S. Stienstra ◽  
T. De Witte
Keyword(s):  
Bone Marrow ◽  
Bone Marrow Transplantation ◽  
Marrow Transplantation ◽  
Cell Populations ◽  
Red Cell ◽  
Flow Cytometric Method ◽  
Flow Cytometric

A novel EGFP-CEM-NKr flow cytometric method for measuring antibody dependent cell mediated-cytotoxicity (ADCC) activity in HIV-1 infected individuals

2006 ◽  
Vol 315 (1-2) ◽  
pp. 1-10 ◽  
Author(s):  
Wannee Kantakamalakul ◽  
Kovit Pattanapanyasat ◽  
Surat Jongrakthaitae ◽  
Vatcharain Assawadarachai ◽  
Silawun Ampol ◽  
...  
Keyword(s):  
Adcc Activity ◽  
Flow Cytometric Method ◽  
Flow Cytometric ◽  
Dependent Cell ◽  
Hiv 1

scholarly journals A 5-color flow cytometric method for extended 8-part leukocyte differential

2017 ◽  
Vol 92 (6) ◽  
pp. 498-507 ◽  
Author(s):  
Julien Guy ◽  
Orianne Wagner-Ballon ◽  
Olivier Pages ◽  
François Bailly ◽  
Jessica Borgeot ◽  
...  
Keyword(s):  
Color Flow ◽  
Flow Cytometric Method ◽  
Flow Cytometric

scholarly journals A flow-cytometric method for continuous measurement of intracellular Ca2+ concentration

2010 ◽  
Vol 77A (11) ◽  
pp. 1091-1097 ◽  
Author(s):  
Alice Vines ◽  
Gethin J. McBean ◽  
Alfonso Blanco-Fernández
Keyword(s):  
Continuous Measurement ◽  
Flow Cytometric Method ◽  
Flow Cytometric

scholarly journals Fluorescence-Activated Cell Sorting of EGFP-Labeled Neural Crest Cells From Murine Embryonic Craniofacial Tissue

2005 ◽  
Vol 2005 (3) ◽  
pp. 232-237 ◽  
Author(s):  
Saurabh Singh ◽  
Vasker Bhattacherjee ◽  
Partha Mukhopadhyay ◽  
Christopher A. Worth ◽  
Samuel R. Wellhausen ◽  
...  
Keyword(s):  
Neural Crest ◽  
Cell Sorting ◽  
Present Report ◽  
Neural Crest Cells ◽  
Egfp Expression ◽  
Marker Genes ◽  
Flow Cytometric Method ◽  
Flow Cytometric ◽  
Polymerase Chain ◽  
Craniofacial Tissue

During the early stages of embryogenesis, pluripotent neural crest cells (NCC) are known to migrate from the neural folds to populate multiple target sites in the embryo where they differentiate into various derivatives, including cartilage, bone, connective tissue, melanocytes, glia, and neurons of the peripheral nervous system. The ability to obtain pure NCC populations is essential to enable molecular analyses of neural crest induction, migration, and/or differentiation. CrossingWnt1-CreandZ/EGtransgenic mouse lines resulted in offspring in which theWnt1-Cretransgene activated permanent EGFP expression only in NCC. The present report demonstrates a flow cytometric method to sort and isolate populations of EGFP-labeled NCC. The identity of the sorted neural crest cells was confirmed by assaying expression of known marker genes by TaqMan Quantitative Real-Time Polymerase Chain Reaction (QRT-PCR). The molecular strategy described in this report provides a means to extract intact RNA from a pure population of NCC thus enabling analysis of gene expression in a defined population of embryonic precursor cells critical to development.

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