• 1 January 1978
    • journal article
    • research article
    • Vol. 39  (11) , 1856-1857
Abstract
A simple method for preparation of highly specific antisera against equine infectious anemia virus proteins p26 and p16 is described. Viral proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The motility of the viral proteins in the gel was compared with standards. Unstained portions of the slab gel were sliced into 5-nm bands, emulsified with Freund''s complete adjuvant, and injected into rabbits to produce specific antisera.