Abstract

<p>(A) The brain homogenates of terminally ill wild-type and tg(PrPΔOR)/<i>Prnp<sup>0/0</sup></i> mice were treated with PNGase F after digestion with PK, and subjected to immunoblotting with M-20 anti-PrP antibodies. The deglycosylated PK-resistant band of PrP<sup>Sc</sup>ΔOR was higher in molecular size than that of full-length PrP<sup>Sc</sup>. Arrows indicates PK-resistant deglycosylated PrPs. (B) The brain homogenates from terminally ill wild-type and tg(PrPΔOR)/<i>Prnp<sup>0/0</sup></i> mice were digested with PK, and subjected to immunoblotting with N-terminus-specific IBL-N anti-PrP antibody. The IBL-N antibodies recognized the PK-resistant PrPs from PrP<sup>Sc</sup>ΔOR but not from full-length PrP<sup>Sc</sup>.</p

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