Clinical Chemistry Link to Randox Laboratories Web Site
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 42: 193-209, 1996;
This Article
Right arrow Full Text (PDF)
Right arrow Submit an electronic Letter to
the Editor about this paper
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Morgan, C. L.
Right arrow Articles by Price, C. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Morgan, C. L.
Right arrow Articles by Price, C. P.

Clinical Chemistry, Vol 42, 193-209, Copyright © 1996 by American Association for Clinical Chemistry

Immunosensors: technology and opportunities in laboratory medicine

CL Morgan, DJ Newman and CP Price
Department of Clinical Biochemistry, St. Bartholomew's and Royal London School of Medicine and Dentistry, London.

An immunosensor is a device comprising an antigen or antibody species coupled to a signal transducer, which detects the binding of the complementary species. An indirect immunosensor uses a separate labeled species that is detected after binding by, e.g., fluorescence or luminescence (i.e., a heterogeneous immunoassay). A direct device detects the binding by a change in potential difference, current, resistance, mass, heat, or optical properties (i.e., a homogeneous immunoassay). Although indirect sensors may encounter fewer problems due to nonspecific binding effects, the direct sensors are capable of real-time monitoring of the antigen-antibody reaction. A wide range of molecules can be detected with detection limits ranging between 10(-9) and 10(-13) mol/L. However, there are only a few successful commercial applications of direct immunosensors, these being of the optical type. This review describes the principles underlying the technologies, their merits, limitations, and applications.


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


Home page
Clin. Chem.Home page
S.-F. Chou, W.-L. Hsu, J.-M. Hwang, and C.-Y. Chen
Determination of {alpha}-Fetoprotein in Human Serum by a Quartz Crystal Microbalance-based Immunosensor
Clin. Chem., June 1, 2002; 48(6): 913 - 918.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
W. Qian, D. Yao, F. Yu, B. Xu, R. Zhou, X. Bao, and Z. Lu
Immobilization of Antibodies on Ultraflat Polystyrene Surfaces
Clin. Chem., September 1, 2000; 46(9): 1456 - 1463.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
S. D. Jayasena
Aptamers: An Emerging Class of Molecules That Rival Antibodies in Diagnostics
Clin. Chem., September 1, 1999; 45(9): 1628 - 1650.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
C. P. Price
The Evolution of Immunoassay as Seen Through the Journal Clinical Chemistry
Clin. Chem., October 1, 1998; 44(10): 2071 - 2074.
[Full Text] [PDF]


Home page
Clin. Chem.Home page
K. Helmerson, R. Kishore, W. D. Phillips, and H. H. Weetall
Optical tweezers-based immunosensor detects femtomolar concentrations of antigens
Clin. Chem., February 1, 1997; 43(2): 379 - 383.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1996 by the American Association for Clinical Chemistry.