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


     


Clinical Chemistry 49: 868-872, 2003; 10.1373/49.6.868
This Article
Right arrow Full Text
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 Web of Science
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 Web of Science (7)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Qiu, L. L.
Right arrow Articles by Elin, R. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Qiu, L. L.
Right arrow Articles by Elin, R. J.
Related Collections
Right arrow Clinical Immunology
Right arrow Proteomics and Protein Markers
(Clinical Chemistry. 2003;49:868-872.)
© 2003 American Association for Clinical Chemistry, Inc.

Convenient and Effective Method for Removing Fibrinogen from Serum Specimens before Protein Electrophoresis

Ling L. Qiu1, Stanley S. Levinson1,2, Kristen L. Keeling1 and Ronald J. Elin1,a

1 Department of Pathology and Laboratory Medicine, University of Louisville School of Medicine, Louisville, KY 40202.

2 Laboratory Service, Veterans’ Administration Medical Center, Louisville, KY 40206-1466.

aAuthor for correspondence. Fax 502-852-8299; e-mail rjelin01{at}gwise.louisville.edu.

Background: Fibrinogen in serum specimens can be misinterpreted on protein electrophoresis as a monoclonal protein. We evaluated selective precipitation of fibrinogen with ethanol.

Methods: Pooled human plasma was mixed with absolute ethanol or saline (final concentrations of 40, 80, 100, 120, and 160 mL/L) and incubated at 4 °C overnight or placed in an ice bath for 15 min. After centrifugation, the supernatants and resuspended pellets were used for protein electrophoresis and quantitative measurements of protein and fibrinogen.

Results: The fibrinogen band was effectively eliminated from the electrophoretic pattern in the plasma samples treated with ethanol at 100 mL/L and incubated in an ice bath for 15 min without a significant change in immunoglobulin concentrations. The 100 mL/L ethanol did not noticeably change the electrophoretic pattern of monoclonal immunoglobulins. This approach allowed analysis of a sample collected from an arteriovenous shunt kept open with heparin.

Conclusions: Ethanol, 100 mL/L, can selectively precipitate fibrinogen without significantly interfering with the immunoglobulins. The precipitation process can be completed in 15 min at 0–4 °C and can avoid the need to obtain another blood sample.




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


Home page
Clin. Chem.Home page
K. Gijbels, G. Marien, and X. Bossuyt
Ethanol Precipitation Is Not Reliable for Selectively Removing Nonmonoclonal Peaks Seen in the Fibrinogen Region on Capillary Zone Electrophoresis of Serum Proteins
Clin. Chem., October 1, 2004; 50(10): 1880 - 1881.
[Full Text] [PDF]


Home page
Clin. Chem.Home page
Y. Ibrahim, M. Volkmann, R. Hassoun, W. Fiehn, H. Rossmann, S. S. Levinson, and R. J. Elin
Serum Protein Electrophoresis: Reptilase Treatment Is Superior to Ethanol Precipitation for Specific Removal of Fibrinogen from Heparinized Plasma Samples * Drs. Levinson and Elin respond:
Clin. Chem., June 1, 2004; 50(6): 1100 - 1101.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by the American Association for Clinical Chemistry.