Hemagglutination: Difference between revisions
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'''Hemagglutination''', or '''haemagglutination''', is a specific form of [[Agglutination (biology)|agglutination]] that involves [[red blood cell]]s (RBCs). It has two common uses in the laboratory: blood typing and the quantification of virus dilutions. |
'''Hemagglutination''', or '''haemagglutination''', is a specific form of [[Agglutination (biology)|agglutination]] that involves [[red blood cell]]s (RBCs). It has two common uses in the laboratory: blood typing and the [[Virus quantification|quantification of virus]] dilutions. |
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==Blood Typing== |
==Blood Typing== |
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Revision as of 20:14, 4 March 2010
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Hemagglutination, or haemagglutination, is a specific form of agglutination that involves red blood cells (RBCs). It has two common uses in the laboratory: blood typing and the quantification of virus dilutions.
Blood Typing
Blood type can be determined by using antibodies that bind to the A or B blood group in a sample of blood.
For example, if antibodies that bind the A blood group are added and agglutination occurs, the blood is either type A or type AB. To determine between type A or type AB, antibodies that bind the B group are added and if agglutination does not occur, the blood is type A.
In blood grouping the patient's serum is tested against RBCs of known blood groups and also the patient's RBCs are tested against known serum types. In this way the patient's blood group is confirmed from both RBCs and serum. A direct Coombs test is also done on the patient's blood sample in case there are any confounding antibodies.
Viral Hemagglutination Assay
Many viruses attach to molecules present on the surface of RBCs. A consequence of this is that at certain concentrations, a viral suspension may bind together (agglutinate) the RBCs, thus preventing them from settling out of suspension. Since agglutination is rarely linked to infectivity,[citation needed] attenuated viruses can therefore be used in assays.
By serially diluting a virus suspension into an assay tray (a series of wells of uniform volume) and adding a standard amount of blood cells, an estimation of the number of virus particles can be made. While less accurate than a plaque assay, it is cheaper and quicker (taking just 30 minutes).
This assay may be modified to include the addition of an antiserum. By using a standard amount of virus, a standard amount of blood cells, and serially diluting the antiserum, one can identify the minimum inhibitory concentration of the antiserum (the greatest dilution which inhibits hemagglutination).
External links
- Hemagglutination: Presented by the University of Virginia
- Hemagglutination at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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