Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 19: 1345-1349, 1973;
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lowden, J. A.
Right arrow Articles by Kaback, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lowden, J. A.
Right arrow Articles by Kaback, M.

Clinical Chemistry, Vol 19, 1345-1349, Copyright © 1973 by the American Association for Clinical Chemistry

Automated Assay of Hexosaminidases in Serum

J. A. Lowden 1, M. A. Skomorowski 1, F. Henderson 1, and M. Kaback 1

1 The Research Institute, The Hospital for Sick Children, Toronto, Canada.

In serum there are two classes of hexosaminidase. One of these is heat-labile and is inactive in children with Tay—Sachs disease. Serum from heterozygotes for Tay—Sachs disease has half the normal activity of the heat-labile enzyme. The heat-labile enzyme can be inactivated by heating serum diluted in buffer for 5 min at 60 °C. We have used this property to develop a reliable, fully automated assay for serum hexosaminidases, which can be used for mass carrier screening programs.


Key Words: Tay—Sachs disease • screening technique • AutoAnalyzer • oral contraceptives • manual and automated methods compared

Submitted on June 29, 1973




The following articles in journals at HighWire Press have cited this article:


Home page
PediatricsHome page
G. H. B. Maegawa, T. Stockley, M. Tropak, B. Banwell, S. Blaser, F. Kok, R. Giugliani, D. Mahuran, and J. T.R. Clarke
The Natural History of Juvenile or Subacute GM2 Gangliosidosis: 21 New Cases and Literature Review of 134 Previously Reported
Pediatrics, November 1, 2006; 118(5): e1550 - e1562.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1973 by the American Association for Clinical Chemistry.