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THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM

Monocytes from blood and from spleen have been cultivated in fluid medium in Carrel flasks for over 2 months. Diluted serum supplied all the essential nutritive substances. Cultivation in fluid was made possible by adjusting the initial pH of the fluid to 7.4, and not allowing it to fall below 7.0 o...

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Detalles Bibliográficos
Autor principal: Baker, Lillian E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1933
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132323/
https://www.ncbi.nlm.nih.gov/pubmed/19870217
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author Baker, Lillian E.
author_facet Baker, Lillian E.
author_sort Baker, Lillian E.
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description Monocytes from blood and from spleen have been cultivated in fluid medium in Carrel flasks for over 2 months. Diluted serum supplied all the essential nutritive substances. Cultivation in fluid was made possible by adjusting the initial pH of the fluid to 7.4, and not allowing it to fall below 7.0 or 6.8. The cells remained in good condition when the pH was adjusted with either lactic acid, hydrochloric acid, or carbon dioxide. Adjustment with carbon dioxide was found to be more convenient and also more practical, since it does not destroy the buffer action of the medium. After 2 months of cultivation, the monocytes were in excellent condition and still proliferated actively. They gave every indication that indefinite multiplication could be maintained under the conditions of these experiments. It is hoped that this method of cultivation, with some modifications, will prove useful in studying the metabolism of these cells.
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spelling pubmed-21323232008-04-18 THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM Baker, Lillian E. J Exp Med Article Monocytes from blood and from spleen have been cultivated in fluid medium in Carrel flasks for over 2 months. Diluted serum supplied all the essential nutritive substances. Cultivation in fluid was made possible by adjusting the initial pH of the fluid to 7.4, and not allowing it to fall below 7.0 or 6.8. The cells remained in good condition when the pH was adjusted with either lactic acid, hydrochloric acid, or carbon dioxide. Adjustment with carbon dioxide was found to be more convenient and also more practical, since it does not destroy the buffer action of the medium. After 2 months of cultivation, the monocytes were in excellent condition and still proliferated actively. They gave every indication that indefinite multiplication could be maintained under the conditions of these experiments. It is hoped that this method of cultivation, with some modifications, will prove useful in studying the metabolism of these cells. The Rockefeller University Press 1933-10-31 /pmc/articles/PMC2132323/ /pubmed/19870217 Text en Copyright © Copyright, 1933, by The Rockefeller Institute for Medical Research New York This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Baker, Lillian E.
THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM
title THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM
title_full THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM
title_fullStr THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM
title_full_unstemmed THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM
title_short THE CULTIVATION OF MONOCYTES IN FLUID MEDIUM
title_sort cultivation of monocytes in fluid medium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132323/
https://www.ncbi.nlm.nih.gov/pubmed/19870217
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