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Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells
Neural retinal cells from 9-d-old chick embryos were assayed for uridine diphosphate (UDP)-galactose:ganglioside GM2 galactosyltransferase, or GM1 synthetase, activity using the oligosaccharide fragment of GM2, oligo-GM2, oligo-GM2, as the exogenous acceptor. The results demonstrated that this enzym...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1982
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112116/ https://www.ncbi.nlm.nih.gov/pubmed/6802857 |
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collection | PubMed |
description | Neural retinal cells from 9-d-old chick embryos were assayed for uridine diphosphate (UDP)-galactose:ganglioside GM2 galactosyltransferase, or GM1 synthetase, activity using the oligosaccharide fragment of GM2, oligo-GM2, oligo-GM2, as the exogenous acceptor. The results demonstrated that this enzyme activity was present on the external surfaces of intact cells. Little difference between the specific activities of cell surface GM1 synthetase could be detected when cells derived from dorsal and ventral segments of the neural retina were compared. These results suggested that this cell- surface enzyme was not present in a concentration gradient along the dorsoventral axis of the neural retina. |
format | Text |
id | pubmed-2112116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1982 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21121162008-05-01 Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells J Cell Biol Articles Neural retinal cells from 9-d-old chick embryos were assayed for uridine diphosphate (UDP)-galactose:ganglioside GM2 galactosyltransferase, or GM1 synthetase, activity using the oligosaccharide fragment of GM2, oligo-GM2, oligo-GM2, as the exogenous acceptor. The results demonstrated that this enzyme activity was present on the external surfaces of intact cells. Little difference between the specific activities of cell surface GM1 synthetase could be detected when cells derived from dorsal and ventral segments of the neural retina were compared. These results suggested that this cell- surface enzyme was not present in a concentration gradient along the dorsoventral axis of the neural retina. The Rockefeller University Press 1982-04-01 /pmc/articles/PMC2112116/ /pubmed/6802857 Text en 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 | Articles Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells |
title | Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells |
title_full | Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells |
title_fullStr | Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells |
title_full_unstemmed | Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells |
title_short | Quantification of ganglioside GM1 synthetase activity on intact chick neural retinal cells |
title_sort | quantification of ganglioside gm1 synthetase activity on intact chick neural retinal cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112116/ https://www.ncbi.nlm.nih.gov/pubmed/6802857 |