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Addgene

cytosolic moPrP (3F4)
(Plasmid #1321)

Full plasmid sequence is not available for this item.

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This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 1321 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pcb6
  • Backbone size w/o insert (bp) 7000
  • Vector type
    Mammalian Expression
  • Selectable markers
    Neomycin (select with G418)

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    Low Copy

Gene/Insert

  • Gene/Insert name
    PrP
  • Alt name
    cytosolic PrP
  • Species
    M. musculus (mouse)
  • Insert Size (bp)
    750
  • Mutation
    N-term truncation (to make gene cytosolic), various mutations to make 3F4 epitope
  • GenBank ID
    NM_011170
  • Entrez Gene
    Prnp (a.k.a. CD230, PrP, PrP<C>, PrPC, PrPSc, Prn-i, Prn-p, Sinc, prP27-30, prP33-35C)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site bglII, EcoRI, KpnI, NotI, ClaI (not destroyed)
  • 3′ cloning site HindIII, XbaI, BamHI (not destroyed)
  • 5′ sequencing primer CMV-F
  • (Common Sequencing Primers)

Resource Information

Terms and Licenses

  • Academic/Nonprofit Terms
  • Industry Terms
    • Not Available to Industry
Trademarks:
  • Zeocin® is an InvivoGen trademark.

Depositor Comments

The signal sequence at the N-terminus was deleted to make it cytosolic instead of lumenal.

How to cite this plasmid ( Back to top)

These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.

  • For your Materials & Methods section:

    cytosolic moPrP (3F4) was a gift from Susan Lindquist (Addgene plasmid # 1321 ; http://n2t.net/addgene:1321 ; RRID:Addgene_1321)
  • For your References section:

    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. 10.1073/pnas.011578098 PubMed 11742063