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Volume 14, Number 2—February 2008
Dispatch

Atypical Bovine Spongiform Encephalopathies, France, 2001–2007

Anne-Gaëlle Biacabe*, Eric Morignat*, Johann Vulin*, Didier Calavas*, and Thierry G.M. Baron*Comments to Author 
Author affiliations: *Agence Française de Sécurité Sanitaire des Aliments, Lyon, France;

Main Article

Figure 2

Representative Western blot analyses of protease-resistant prion protein (PrPres) in H-type (lanes 2, 3), L-type (lanes 5, 6), and C-type (lanes 1, 4, 7) cases of bovine spongiform encephalopathy (BSE). Bars to the left of the panels indicate the 29.0-, 20.1-, and 14.3-kDa marker positions. H-type, higher molecular masses of unglycosylated PrPres; L-type, lower molecular masses of unglycosylated PrPres; C-type, classic BSE. Monoclonal antibodies Sha31 and SAF84 were used for PrPres detection in panels A and B, respectively.

Figure 2. Representative Western blot analyses of protease-resistant prion protein (PrPres) in H-type (lanes 2, 3), L-type (lanes 5, 6), and C-type (lanes 1, 4, 7) cases of bovine spongiform encephalopathy (BSE). Bars to the left of the panels indicate the 29.0-, 20.1-, and 14.3-kDa marker positions. H-type, higher molecular masses of unglycosylated PrPres; L-type, lower molecular masses of unglycosylated PrPres; C-type, classic BSE. Monoclonal antibodies Sha31 and SAF84 were used for PrPres detection in panels A and B, respectively.

Main Article

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