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Addgene

pTH734-2µ-RLuc/stopCFLuc
(Plasmid #40609)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 40609 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pBEVY-U
  • Backbone manufacturer
    Miller et al (1998) Nucleic Acids Res 26(15):3577-3583
  • Backbone size w/o insert (bp) 6518
  • Total vector size (bp) 7466
  • Vector type
    Yeast Expression
  • Selectable markers
    URA3

Growth in Bacteria

  • Bacterial Resistance(s)
    Ampicillin, 100 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Growth instructions
    We have observed that plasmids containing the codon maximised Firefly luciferase variant or portions there of cause slow growth in some E. coli strains (eg Top10). However, this does not appear to affect plasmid yield.
  • Copy number
    High Copy

Gene/Insert 1

  • Gene/Insert name
    Firefly Luciferase (nonsense mutant)
  • Alt name
    FLuc
  • Species
    Photinus pyralis
  • Insert Size (bp)
    1650
  • Mutation
    All codons of the original FLuc gene were exchanged for those isoaccepting codons decoded by the most abundant tRNAs in yeast. The last three codons of the full-length Firefly luciferase gene have been deleted to yield a luciferase variant which is fully functional, but no longer localises to peroxisomes. Codon 5 of the FLuc ORF was exchanged for a stop codon (TAG).
  • GenBank ID
    AF043450
  • Promoter TDH3

Cloning Information for Gene/Insert 1

  • Cloning method Restriction Enzyme
  • 5′ cloning site BamHI (not destroyed)
  • 3′ cloning site SalI (not destroyed)
  • 5′ sequencing primer TDH3
  • 3′ sequencing primer M13r
  • (Common Sequencing Primers)

Gene/Insert 2

  • Gene/Insert name
    Renilla luciferase
  • Alt name
    RLuc
  • Species
    Synthetic; Renilla reniformis
  • Insert Size (bp)
    942
  • GenBank ID
    AF043450.1
  • Promoter ADH1

Cloning Information for Gene/Insert 2

  • Cloning method Restriction Enzyme
  • 5′ cloning site XmaI (not destroyed)
  • 3′ cloning site EcoRI (not destroyed)
  • 5′ sequencing primer ADH1
  • 3′ sequencing primer unknown
  • (Common Sequencing Primers)

Resource Information

  • A portion of this plasmid was derived from a plasmid made by
    The RLuc gene originated from a plasmid kindly provided by Dr David Bedwell (University of Alabama, Birmingham). Salas-Marco J, Bedwell DM (2004) Molecular and Cellular Biology 24:7769-7778.

Terms and Licenses

Trademarks:
  • Zeocin® is an InvivoGen trademark.
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:

    pTH734-2µ-RLuc/stopCFLuc was a gift from Tobias von der Haar (Addgene plasmid # 40609 ; http://n2t.net/addgene:40609 ; RRID:Addgene_40609)
  • For your References section:

    Translation elongation can control translation initiation on eukaryotic mRNAs. Chu D, Kazana E, Bellanger N, Singh T, Tuite MF, von der Haar T. EMBO J. 2014 Jan 1;33(1):21-34. doi: 10.1002/embj.201385651. Epub 2013 Dec 19. 10.1002/embj.201385651 PubMed 24357599