Description
Prion Protein (PrP) and namely its abnormal isoform, partially reistant 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. A03212]
Synonyms: PrP
Immunogen: human recombinant prion protein
Formulation: Lyophilized IgG
Isotype: IgG
Applications: EIA, FC, and WB
Origin: Animal/Mouse
Stability: 730 days
Application|ELISA||Application|Flow Cytometry||Application|Western Blot||Product Type|Antibodies|Monoclonal Antibodies||Research Area|Neuroscience|Neurodegenerative Disorders|Prion Disease
