Prion Protein (PrP) and namely its abnormal isoform, partially resistant to proteinase K (PrPres), is the only specific molecular marker of the Transmissible Spongiform Encephalopathies (TSEs) such as Bovine Spongiform Encephalopathie (BSE) or its huma...More
|Stability||Store at -20degrees;shelf life 2 years maximum after production|
|Antigen||This anti-prion Protein Monoclonal Antibody was raised against a synthetic peptide representative of the human 106-126 sequence|
|Label||Labelling upon request|
Reconstitute the content of the vial in 1 mL of water.
For EIA, the optimal working dilution must be determined empirically (currently between 0.1 and 1 µg/mL). For western blot analysis of PrPc, dilute the antibody to a final concentration of 1 µ
|Application Media||Reconstitute the content of the vial in 1 mL of water.|
|Formulation||lyophilized IgG with BSA|
Demart S., et al. New Insight into Abnormal Prion Protein Using Monoclonal Antibodies.Biochemical and Biophysical Research Communications 265, 652-657 (1999).
Rodolfo K., et al. A novel cellular prion protein isoform present in rapid anterograde axonal tr