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Addgene

pTriEx-HTNC
(Plasmid #13763)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 13763 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pTriEx-1
  • Backbone manufacturer
    Novagen
  • Backbone size w/o insert (bp) 5612
  • Vector type
    Bacterial Expression ; Baculovirus

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    TAT-NLS-Cre
  • Alt name
    TAT-Cre
  • Alt name
    HTNC
  • Alt name
    HTNCre
  • Species
    NLS from SV40, TAT from HIV, and Cre from bacteriophage P1
  • Insert Size (bp)
    932
  • Tags / Fusion Proteins
    • His Tag (N terminal on insert)
    • TAT (N terminal on insert)
    • NLS (N terminal on insert)

Cloning Information

  • Cloning method Restriction Enzyme
  • 5′ cloning site NcoI (unknown if destroyed)
  • 3′ cloning site XhoI (unknown if destroyed)
  • 5′ sequencing primer T7
  • (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

Please also acknowledge Dr. Frank Edenhofer when using this plasmid in publications.

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:

    pTriEx-HTNC was a gift from Klaus Rajewsky (Addgene plasmid # 13763 ; http://n2t.net/addgene:13763 ; RRID:Addgene_13763)
  • For your References section:

    Ability of the hydrophobic FGF and basic TAT peptides to promote cellular uptake of recombinant Cre recombinase: a tool for efficient genetic engineering of mammalian genomes. Peitz M, Pfannkuche K, Rajewsky K, Edenhofer F. Proc Natl Acad Sci U S A. 2002 Apr 2. 99(7):4489-94. 10.1073/pnas.032068699 PubMed 11904364