<p>(<b>A</b>) Activity of pAb RVC and RTC, as compared to the established mAb 6H4, against normal brain homogenates from bovine, mouse, humans and hamster. (<b>B</b>) Human and mouse normal brain homogenates were immunoblotted with pAb RVC and RTC alone or in the presence of diverse Helix-3 PrP peptides (see <a href="http://www.plospathogens.org/article/info:doi/10.1371/journal.ppat.1000977#ppat-1000977-g001" target="_blank">Figure 1C</a> for the peptide sequences) (<b>C</b>) Brain homogenates from mice, hamster and humans (normal, prion-infected and prion-infected digested with proteinase K), were immunoblotted with mAb 6H4, with pAb RTC or RVC, or with rec Ab R1. D) Mouse scrapie (RML) and human CJD brains (E200K) were digested with PK, p...
The human prion diseases, such as variant Creutzfeldt-Jakob disease (vCJD), are characterized by the...
<p>All mice were inoculated with the same vCJD prion isolate. Immunoblots were analysed by enhanced ...
Prion diseases are a group of fatal neurodegenerative disorders that affect humans and animals. They...
<p><b>(A)</b> RT-QuIC analyses failed to reveal <i>de novo</i> PrP<sup>Sc</sup> aggregation when see...
<p>(<b>A</b>) Brain (normal, scrapie infected, as well as scrapie infected digested with PK) as well...
Prion diseases are a group of rare, fatal neurodegenerative disorders associated with a conformation...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
<p>(A) PrioV3 antibody was screened with 20-mer amino acid sequences spanning the 91–230 region of t...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prion diseases are a group of fatal neurodegenerative disorders that affect humans and animals. They...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
By immunizing prion knockout mice (Prnp-/-) with recombinant murine prion protein (PrPc), we obtaine...
<p>The anti-PrP monoclonal antibodies used were, ICSM 18 (panels A, C, E, G) that recognizes both hu...
The availability of specific monoclonal antibodies (mAbs) recognizing the aberrant form (PrP(Sc)) of...
The human prion diseases, such as variant Creutzfeldt-Jakob disease (vCJD), are characterized by the...
<p>All mice were inoculated with the same vCJD prion isolate. Immunoblots were analysed by enhanced ...
Prion diseases are a group of fatal neurodegenerative disorders that affect humans and animals. They...
<p><b>(A)</b> RT-QuIC analyses failed to reveal <i>de novo</i> PrP<sup>Sc</sup> aggregation when see...
<p>(<b>A</b>) Brain (normal, scrapie infected, as well as scrapie infected digested with PK) as well...
Prion diseases are a group of rare, fatal neurodegenerative disorders associated with a conformation...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
<p>(A) PrioV3 antibody was screened with 20-mer amino acid sequences spanning the 91–230 region of t...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
Prion diseases are a group of fatal neurodegenerative disorders that affect humans and animals. They...
Human prion diseases are characterized by the conversion of the normal host cellular prion protein (...
By immunizing prion knockout mice (Prnp-/-) with recombinant murine prion protein (PrPc), we obtaine...
<p>The anti-PrP monoclonal antibodies used were, ICSM 18 (panels A, C, E, G) that recognizes both hu...
The availability of specific monoclonal antibodies (mAbs) recognizing the aberrant form (PrP(Sc)) of...
The human prion diseases, such as variant Creutzfeldt-Jakob disease (vCJD), are characterized by the...
<p>All mice were inoculated with the same vCJD prion isolate. Immunoblots were analysed by enhanced ...
Prion diseases are a group of fatal neurodegenerative disorders that affect humans and animals. They...