Enzyme-linked immunosorbent assay: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Robert Badgett
(New page: {{subpages}} '''Enzyme-linked immunosorbent assays''' (ELISA) are "an immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either t...)
 
imported>Robert Badgett
No edit summary
Line 1: Line 1:
{{subpages}}
{{subpages}}
'''Enzyme-linked immunosorbent assays''' (ELISA) are "an [[immunoassay]] utilizing an [[antibody]] labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the [[antigen]] and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed."<ref>{{MeSH}}</ref>
'''Enzyme-linked immunosorbent assays''' (ELISA) are "an [[immunoassay]] utilizing an [[antibody]] labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an [[Immunosorbent technique|immunosorbent]] substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the [[antigen]] and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed."<ref>{{MeSH}}</ref>


==References==
==References==
<references/>
<references/>

Revision as of 00:07, 22 June 2009

This article is a stub and thus not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.

Enzyme-linked immunosorbent assays (ELISA) are "an immunoassay utilizing an antibody labeled with an enzyme marker such as horseradish peroxidase. While either the enzyme or the antibody is bound to an immunosorbent substrate, they both retain their biologic activity; the change in enzyme activity as a result of the enzyme-antibody-antigen reaction is proportional to the concentration of the antigen and can be measured spectrophotometrically or with the naked eye. Many variations of the method have been developed."[1]

References