Parvalbumins are highly stable Ca2+ binding proteins, present in large
quantities in the sarcoplasmic reticulum in the white muscle of most
lower vertebrates and fish. The properties of these proteins make them
promising antigens for the use as a specific biomarker for fish speci
es identification. Parvalbumin isotypes were isolated, on a preparativ
e scale level, by use of size exclusion chromatography (SEC) and anion
exchange HPLC. The utility of this technique, with regard to maximizi
ng purified isotypes, is discussed.