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CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS

The techniques described permit the controlled production of large numbers of proliferating somatic cell hybrids in a relatively short period of time. Sendai virus is used to promote cell hybridization. β-propriolactone is employed as the inactivating agent of Sendai virus since it produces complete...

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Detalles Bibliográficos
Autores principales: Klebe, Robert J., Chen, Tchaw-Ren, Ruddle, Frank H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1970
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2107999/
https://www.ncbi.nlm.nih.gov/pubmed/4318843
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author Klebe, Robert J.
Chen, Tchaw-Ren
Ruddle, Frank H.
author_facet Klebe, Robert J.
Chen, Tchaw-Ren
Ruddle, Frank H.
author_sort Klebe, Robert J.
collection PubMed
description The techniques described permit the controlled production of large numbers of proliferating somatic cell hybrids in a relatively short period of time. Sendai virus is used to promote cell hybridization. β-propriolactone is employed as the inactivating agent of Sendai virus since it produces complete loss of viral infectivity while preserving viral fusion capacity. Cells are fused in monolayer, instead of in suspension, since fixing cells in two dimensions permits one to control cell contacts during the fusion event through the expedient of varying multiplicities of the parental cells and the total cell density. Under the conditions described, a several hundred fold increase in the number of hybrid clones obtained is seen as compared to the controls.
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spelling pubmed-21079992008-05-01 CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS Klebe, Robert J. Chen, Tchaw-Ren Ruddle, Frank H. J Cell Biol Article The techniques described permit the controlled production of large numbers of proliferating somatic cell hybrids in a relatively short period of time. Sendai virus is used to promote cell hybridization. β-propriolactone is employed as the inactivating agent of Sendai virus since it produces complete loss of viral infectivity while preserving viral fusion capacity. Cells are fused in monolayer, instead of in suspension, since fixing cells in two dimensions permits one to control cell contacts during the fusion event through the expedient of varying multiplicities of the parental cells and the total cell density. Under the conditions described, a several hundred fold increase in the number of hybrid clones obtained is seen as compared to the controls. The Rockefeller University Press 1970-04-01 /pmc/articles/PMC2107999/ /pubmed/4318843 Text en Copyright © 1970 by The Rockefeller University Press 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
Klebe, Robert J.
Chen, Tchaw-Ren
Ruddle, Frank H.
CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS
title CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS
title_full CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS
title_fullStr CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS
title_full_unstemmed CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS
title_short CONTROLLED PRODUCTION OF PROLIFERATING SOMATIC CELL HYBRIDS
title_sort controlled production of proliferating somatic cell hybrids
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2107999/
https://www.ncbi.nlm.nih.gov/pubmed/4318843
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