DocumentCode :
2143939
Title :
Parvalbumins as a biomarker for fish species identification: applications to snook (Centropomus undecimalis) preservation
Author :
Tilghman, R.W. ; Ross, C.I. ; Mari, F. ; Hartmann, J.X.
Author_Institution :
Depts. of Biol. Sci., Chem. & Biochem., Florida Atlantic Univ., Boca Raton, FL, USA
Volume :
3
fYear :
1996
fDate :
23-26 Sep 1996
Firstpage :
1372
Abstract :
Parvalbumins are highly stable Ca2+ binding proteins found predominantly in the skeletal muscles of vertebrates. The properties of these proteins make them an ideal candidate for use as a specific biomarker for fish identification. Parvalbumins were initially purified from white muscle of the fish species Centropomus undecimalis using ammonium sulfate precipitation and gel filtration. The heterogeneity of the parvalbumins was typified by their separation into 7 isotypes. A dilution endpoint immunoassay was developed for snook parvalbumin using a monoclonal antibody directed against its highly conserved calcium binding site. The utility of specific monoclonal antibodies against fish parvalbumin with regards to species identification is discussed
Keywords :
aquaculture; biological techniques; molecular biophysics; muscle; oceanographic techniques; proteins; zoology; Centropomus undecimalis; NH4SO4; biomarker; fish species; fish stock preservation; fishing industry; forensic science; gel filtration; immunoassay; law enforcement; marine animal; marine biology; measurement technique; molecular biology; monoclonal antibody; ocean; parvalbumin; precipitation; protein; sea; skeletal muscle; snook; taxonomic identification; taxonomy; vertebrate zoology; Biology; Biomarkers; Immune system; Laboratories; Law enforcement; Marine animals; Muscles; Proteins; Solids; Testing;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
OCEANS '96. MTS/IEEE. Prospects for the 21st Century. Conference Proceedings
Conference_Location :
Fort Lauderdale, FL
Print_ISBN :
0-7803-3519-8
Type :
conf
DOI :
10.1109/OCEANS.1996.569103
Filename :
569103
Link To Document :
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