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. A03223]
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Antigen: ovine recombinant PrP • Host: mouse, clone BAR 233 • Isotype: IgG2b • Application(s): EIA, FC, and WB
Synonyms: PrP
Immunogen: ovine recombinant prion protein
Formulation: Lyophilized IgG
Isotype: IgG2b
Applications: EIA, FC, and WB
Origin: Animal/Sheep
Stability: 730 days
Application|ELISA||Application|Flow Cytometry||Application|Western Blot||Product Type|Antibodies|Monoclonal Antibodies||Research Area|Neuroscience|Neurodegenerative Disorders|Prion Disease
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