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A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues

Experimental evidence supporting the postulated analogy between myelin basic protein and a previously described common tumour specific antigen is summarized under antigenic cross-reactivity, subcellular localization, molecular size, basicity and proteolipid nature. A third protein antigen, present i...

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Detalles Bibliográficos
Autores principales: Dickinson, J. P., McDermott, J. R., Smith, J. K., Caspary, E. A.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1974
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009113/
https://www.ncbi.nlm.nih.gov/pubmed/4527605
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author Dickinson, J. P.
McDermott, J. R.
Smith, J. K.
Caspary, E. A.
author_facet Dickinson, J. P.
McDermott, J. R.
Smith, J. K.
Caspary, E. A.
author_sort Dickinson, J. P.
collection PubMed
description Experimental evidence supporting the postulated analogy between myelin basic protein and a previously described common tumour specific antigen is summarized under antigenic cross-reactivity, subcellular localization, molecular size, basicity and proteolipid nature. A third protein antigen, present in all tissues, also shows strong similarities in all these respects.
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spelling pubmed-20091132009-09-10 A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues Dickinson, J. P. McDermott, J. R. Smith, J. K. Caspary, E. A. Br J Cancer Articles Experimental evidence supporting the postulated analogy between myelin basic protein and a previously described common tumour specific antigen is summarized under antigenic cross-reactivity, subcellular localization, molecular size, basicity and proteolipid nature. A third protein antigen, present in all tissues, also shows strong similarities in all these respects. Nature Publishing Group 1974-06 /pmc/articles/PMC2009113/ /pubmed/4527605 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Articles
Dickinson, J. P.
McDermott, J. R.
Smith, J. K.
Caspary, E. A.
A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues
title A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues
title_full A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues
title_fullStr A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues
title_full_unstemmed A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues
title_short A Common Tumour Specific Antigen: II. Further Characterization of the Whole Antigen and of a Cross-Reacting Antigen of Normal Tissues
title_sort common tumour specific antigen: ii. further characterization of the whole antigen and of a cross-reacting antigen of normal tissues
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009113/
https://www.ncbi.nlm.nih.gov/pubmed/4527605
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