A technique for determining E rosette levels by cytofluorographic analysis

A technique for determining E rosette levels by cytofluorographic analysis

A method is described for determining the percentage of rosettes formed by sheep erythrocytes and human peripheral lymphocytes (ER) using cytofluorographic analysis (CFGA). The technique utilizes acridine orange dye for differentially staining nucleus and cytoplasm of the lymphocytes to distinguish...

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Veröffentlicht in:Journal of immunological methods 1976-01, Vol.12 (1), p.9-17
Hauptverfasser: Goldberg, Nelson H., Kenady, Daniel E., Super, Bernard S., Chretie, Paul B.
Format: Artikel
Sprache:eng
Schlagworte:
Acridines
Erythrocytes - immunology
Glutaral
Humans
Immunologic Techniques
Lymphocytes - immunology
Spectrometry, Fluorescence
Time Factors
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container_title Journal of immunological methods
container_volume 12
creator Goldberg, Nelson H.
Kenady, Daniel E.
Super, Bernard S.
Chretie, Paul B.
description A method is described for determining the percentage of rosettes formed by sheep erythrocytes and human peripheral lymphocytes (ER) using cytofluorographic analysis (CFGA). The technique utilizes acridine orange dye for differentially staining nucleus and cytoplasm of the lymphocytes to distinguish them from erythroctes, and glutaraldehyde for fixation of the rosettes. This technique was compared with light microscope counting (LMC) of ER. CFGA gave similar results with better reproducibility than LMC, entailed less time for counting, and markedly reduced operator fatigue.
doi_str_mv 10.1016/0022-1759(76)90091-0
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Acridines
Erythrocytes - immunology
Glutaral
Humans
Immunologic Techniques
Lymphocytes - immunology
Spectrometry, Fluorescence
Time Factors
title A technique for determining E rosette levels by cytofluorographic analysis
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