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Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation.

Ma J, Lindquist S

Proc Natl Acad Sci U S A 2001 Dec 18;98(26):14955-60. Epub 2001 Dec 11. PubMed Journal

ID Plasmid
1319 moPrP(3F4) D177N Add to Cart
1321 cytosolic moPrP (3F4) Add to Cart
13917 mSecPrP-pCB6+ Add to Cart