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. A03200]
Synonyms: PrP
Immunogen: human prion amino acids 106-126 (GAAAAGAVVGGLGGYMLGSAM){7003}
Formulation: 200 µg lyophilized IgG containing 200 µg BSA
Isotype: IgG
Applications: IHC and WB
Origin: Animal/Mouse
Stability: 730 days
Application|ELISA||Application|Western Blot||Product Type|Antibodies|Monoclonal Antibodies||Research Area|Immunology & Inflammation||Research Area|Infectious Disease||Research Area|Neuroscience|Neurodegenerative Disorders|Prion Disease
