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. A03220]
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Antigen: recombinant human PrP • Host: mouse, clone 8G8 • Application(s): IHC
Synonyms: PrP
Immunogen: recombinant human prion protein
Formulation: Lyophilized IgG
Isotype: IgG
Applications: IHC
Origin: Animal/Mouse
Stability: 730 days
Application|Immunohistochemistry||Product Type|Antibodies|Monoclonal Antibodies||Research Area|Immunology & Inflammation||Research Area|Infectious Disease||Research Area|Neuroscience|Neurodegenerative Disorders|Prion Disease
For quantitative detection of human LILRA3 in cell culture supernates, serum and plasma (heparin, EDTA, citrate).
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For the quantitation of Human BDNF concentrations in cell culture supernates, cell lysates, serum and plasma (heparin, EDTA, citrate).
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For the quantitation of Human TIMP3 concentrations in cell culture supernates, serum, plasma(heparin , EDTA) and saliva.
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