An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy.

Antibodies to the prion protein (PrP) have been critical to the neuropathological and biochemical characterization of PrP-related degenerative diseases in humans and animals. Although PrP is highly conserved evolutionarily, there is some sequence divergence among species; as a consequence, anti-PrP...

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Detalhes bibliográficos
Main Authors: Piccardo, P., Langeveld, J. P., Hill, A. F., Dlouhy, S. R., Young, K., Giaccone, G., Rossi, G., Bugiani, M., Bugiani, O., Meloen, R. H., Collinge, J., Tagliavini, F., Ghetti, B.
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1858454/
https://ncbi.nlm.nih.gov/pubmed/9626045
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