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Carcinoembryonic Antigen in Whole Serum

A microradioimmunoassay technique is described for detecting carcinoembryonic antigen (CEA) in whole serum. It differs from previous methods in being performed on 0·025 ml of whole serum instead of 5 ml of serum extracted with perchloric acid. The present assay was sufficiently sensitive to detect 8...

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Detalles Bibliográficos
Autores principales: MacSween, J. M., Warner, N. L., Bankhurst, A. D., Mackay, I. R.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008638/
https://www.ncbi.nlm.nih.gov/pubmed/4117478
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author MacSween, J. M.
Warner, N. L.
Bankhurst, A. D.
Mackay, I. R.
author_facet MacSween, J. M.
Warner, N. L.
Bankhurst, A. D.
Mackay, I. R.
author_sort MacSween, J. M.
collection PubMed
description A microradioimmunoassay technique is described for detecting carcinoembryonic antigen (CEA) in whole serum. It differs from previous methods in being performed on 0·025 ml of whole serum instead of 5 ml of serum extracted with perchloric acid. The present assay was sufficiently sensitive to detect 85% of carcinomata, localized to the colon, but positive results occurred also with certain non-gastrointestinal cancers, chiefly lung and breast, and certain non-malignant diseases. Many of the latter sera, with the general exception of alcoholic cirrhosis and pancreatitis, gave negative results after extraction with perchloric acid. It is suggested that a direct assay for CEA in whole serum may permit testing of large numbers of sera by laboratories with facilities for radioimmunoassays.
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spelling pubmed-20086382009-09-10 Carcinoembryonic Antigen in Whole Serum MacSween, J. M. Warner, N. L. Bankhurst, A. D. Mackay, I. R. Br J Cancer Articles A microradioimmunoassay technique is described for detecting carcinoembryonic antigen (CEA) in whole serum. It differs from previous methods in being performed on 0·025 ml of whole serum instead of 5 ml of serum extracted with perchloric acid. The present assay was sufficiently sensitive to detect 85% of carcinomata, localized to the colon, but positive results occurred also with certain non-gastrointestinal cancers, chiefly lung and breast, and certain non-malignant diseases. Many of the latter sera, with the general exception of alcoholic cirrhosis and pancreatitis, gave negative results after extraction with perchloric acid. It is suggested that a direct assay for CEA in whole serum may permit testing of large numbers of sera by laboratories with facilities for radioimmunoassays. Nature Publishing Group 1972-10 /pmc/articles/PMC2008638/ /pubmed/4117478 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
MacSween, J. M.
Warner, N. L.
Bankhurst, A. D.
Mackay, I. R.
Carcinoembryonic Antigen in Whole Serum
title Carcinoembryonic Antigen in Whole Serum
title_full Carcinoembryonic Antigen in Whole Serum
title_fullStr Carcinoembryonic Antigen in Whole Serum
title_full_unstemmed Carcinoembryonic Antigen in Whole Serum
title_short Carcinoembryonic Antigen in Whole Serum
title_sort carcinoembryonic antigen in whole serum
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008638/
https://www.ncbi.nlm.nih.gov/pubmed/4117478
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