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]
Available on backorder
Antigen: human recombinant prion protein • Host: mouse, clone 11C6 • Isotype: IgG • Application(s): EIA, FC, and WB
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
For the quantitation of Rat Bdnf concentrations in cell culture supernates, cell lysates, serum and plasma (heparin, EDTA, citrate).
Available on backorder
For quantitative detection of human BMPER in cell culture supernates, serum and plasma (heparin, EDTA, citrate).
Available on backorder
For quantitative detection of human LILRA5 in cell culture supernates, serum and plasma (heparin, EDTA, citrate).
Available on backorder
