Description
Prion Protein (PrP) and namely its abnormal isoform, partially resistant to proteinase K (PrPres), is the only specific molecular marker of the Transmissible Spongiform Encephalopathies (TSEs) such as Bovine Spongiform Encephalopathie (BSE) or its human form, the New Variant of Creutzfeld-Jakob disease. [Bertin Catalog No. A03213]
Synonyms: PrP
Immunogen: protein kinase treated and non-denaturated SAF from Syrian Hamster
Formulation: Ascitic liquid lyophilized
Isotype: IgG1
Applications: EIA and WB
Origin:
Stability: 180 days
Application|ELISA||Application|Western Blot||Product Type|Antibodies|Monoclonal Antibodies||Research Area|Neuroscience|Neurodegenerative Disorders|Prion Disease
