Techniques in Prion Research
. Ed(S): Lehmann, Sylvain; Grassi, Jacques
Prion diseases, also known as Transmissible Spongiform Encephalopathies (TSEs), exist in both humans (Creutzfeldt-Jakob disease (CJD)) and animals (scrapie, bovine spongiform encephalopathy (BSE), chronic wasting disease) and have the unique property of being infectious, sporadic or genetic in origin.
Although the precise nature of the infectious agent responsible for TSEs is not definitely identified, it is now clearly demonstrated that a protein named PrP (for Prion Protein) plays a critical role in the transmission and pathogenesis of TSEs.
This book provides the general description as well as the details of the techniques currently used for the study of prion diseases. ... Read more
Features:
Purification of PrPC and the Pathological Isoform of Prion Protein (PrPsc or PrP-res)
Animal Models of TSEs
Cell Culture Models of TSEs
PrPsc Immunohistochemistry
Western Immunoblotting Techniques
Antibody Production and ELISA
TSE Strain Typing in Mice
Biosafety and Decontamination Procedures
Cell-free Conversion of Prion Proteins
Cytotoxicity of PrP Peptides
Cyclic Amplification of Prion Protein Misfolding<
Of interest to:
Researchers and clinicians in the fields of cell biology, biomedicine, neuroscience/neuropathology, veterinary medicine and biochemistry.
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