(.jpg) Embryonic fibroblasts (MEF) of ADAM10 knockout mice accumulate PrPC. Representative western blot of media supernatants and lysates of wild-type (WT) and ADAM10 KO MEF. Lack of shedding and no increased compensatory release of PrP is observed in ADAM10 KO cells. ADAM10 is shown in lysates as a proof of genotypes. Increased levels of PrPC are found in lysates and quantified by referring to β-actin (n = 8; p = 0.00005). (JPEG 131 kb
and Table S2. Oligonucleotides used for qPCR of mouse specific genes & Protein spots differentially ...
The cellular prion protein (PrPC) is one of the most studied mammalian proteins. Despite the ongoing...
Prion diseases are fatal, transmissible neurodegenerative diseases which are associated with the con...
(.jpg) Preference for the shedding of fl-PrP over truncated C1 fragment indicates a role of the N-te...
(.jpg) Quantification of fl-PrP levels and ratio of sPrP/fl-PrP in Sort1 knockout mice. These quanti...
(.jpg) Use of the sPrPG228 antibody for immunohistochemical stainings. Sagittal brain sections of a ...
(.jpg) Species specificity of the sPrPG228 antibody. (A) Comparison of the C-terminal amino acid seq...
(.jpg) Side-by-side comparison of SWA and TM treatments and enzymatic deglycosylation reactions. Wes...
The cellular prion protein (PrP C) is essential for the pathogenesis and transmission of prion disea...
Abstract Background Proteolytic processing of the prion protein (PrPC) by endogenous proteases gener...
Abstract Background The cellular prion protein (PrPC) fulfils several yet not completely understood ...
The prion protein (PrPC) is subjected to several conserved endoproteolytic events producing bioactiv...
(.jpg) Exosome characterization using the NanoSight system. Representative experiment showing the ra...
Prions consist of aggregates of abnormal conformers of the cellular prion protein (PrPC). They propa...
Figure S1. Analysis of APP levels in uninoculated AppNL-F mice. a Immunoblots of brain homogenates f...
and Table S2. Oligonucleotides used for qPCR of mouse specific genes & Protein spots differentially ...
The cellular prion protein (PrPC) is one of the most studied mammalian proteins. Despite the ongoing...
Prion diseases are fatal, transmissible neurodegenerative diseases which are associated with the con...
(.jpg) Preference for the shedding of fl-PrP over truncated C1 fragment indicates a role of the N-te...
(.jpg) Quantification of fl-PrP levels and ratio of sPrP/fl-PrP in Sort1 knockout mice. These quanti...
(.jpg) Use of the sPrPG228 antibody for immunohistochemical stainings. Sagittal brain sections of a ...
(.jpg) Species specificity of the sPrPG228 antibody. (A) Comparison of the C-terminal amino acid seq...
(.jpg) Side-by-side comparison of SWA and TM treatments and enzymatic deglycosylation reactions. Wes...
The cellular prion protein (PrP C) is essential for the pathogenesis and transmission of prion disea...
Abstract Background Proteolytic processing of the prion protein (PrPC) by endogenous proteases gener...
Abstract Background The cellular prion protein (PrPC) fulfils several yet not completely understood ...
The prion protein (PrPC) is subjected to several conserved endoproteolytic events producing bioactiv...
(.jpg) Exosome characterization using the NanoSight system. Representative experiment showing the ra...
Prions consist of aggregates of abnormal conformers of the cellular prion protein (PrPC). They propa...
Figure S1. Analysis of APP levels in uninoculated AppNL-F mice. a Immunoblots of brain homogenates f...
and Table S2. Oligonucleotides used for qPCR of mouse specific genes & Protein spots differentially ...
The cellular prion protein (PrPC) is one of the most studied mammalian proteins. Despite the ongoing...
Prion diseases are fatal, transmissible neurodegenerative diseases which are associated with the con...