Anti-Prion Protein (Clone Pri 308)

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. A03200]Synonyms: PrP. Immunogen: human prion amino acids 106-126 (GAAAAGAVVGGLGGYMLGSAM){7003}. Clone Designation: Pri 308. Formulation: (Request formulation change), 200 µg lyophilized IgG containing 200 µg BSA. Host: Mouse. Isotype: IgG. Applications: IHC and WB. Origin: Animal/Mouse.