Skip to main content
This website uses cookies to ensure you get the best experience. By continuing to use this site, you agree to the use of cookies.

Please note: Your browser does not support the features used on Addgene's website. You may not be able to create an account or request plasmids through this website until you upgrade your browser. Learn more

Please note: Your browser does not fully support some of the features used on Addgene's website. If you run into any problems registering, depositing, or ordering please contact us at [email protected]. Learn more

Addgene

pPBO.ACT001
(Plasmid #182711)

Ordering

Item Catalog # Description Quantity Price (USD)
Plasmid 182711 Standard format: Plasmid sent in bacteria as agar stab 1 $85

This material is available to academics and nonprofits only.

Backbone

  • Vector backbone
    p15a ORI
  • Backbone size w/o insert (bp) 2761
  • Total vector size (bp) 5716
  • Modifications to backbone
    N/A
  • Vector type
    Bacterial Expression, CRISPR

Growth in Bacteria

  • Bacterial Resistance(s)
    Kanamycin, 50 μg/mL
  • Growth Temperature
    37°C
  • Growth Strain(s)
    DH5alpha
  • Copy number
    Low Copy

Gene/Insert

  • Gene/Insert name
    dCasRx
  • Alt name
    dRfxCas13d
  • Alt name
    dCas13
  • Species
    Ruminococcus flavefaciens XPD3002
  • Insert Size (bp)
    2955
  • Mutation
    Catalytically deactivated R295A, H300A, R849A, H854A
  • GenBank ID
    891778
  • Promoter pTet
  • Tag / Fusion Protein
    • 2x-FLAG (C terminal on insert)

Cloning Information

  • Cloning method Gibson Cloning
  • 5′ sequencing primer taagcagctctaatgcgc
  • 3′ sequencing primer gatttcgtgatgcttgtcaggg
  • (Common Sequencing Primers)

Resource Information

  • Supplemental Documents
  • A portion of this plasmid was derived from a plasmid made by
    Plasmid pPBO.ACT001 was built using a dCasRx construct obtained from Emeric Charles at the University of California at Berkeley's labs of David Savage and Jennifer Doudna. Please cite the associated publication in any use of this plasmid: https://doi.org/10.1101/2021.05.26.445687. dCasRx was originally identified and created by Silvana Konnerman et al in the following publication. A variant of dCasRx can be obtained from Addgene deposit #109050. Please also cite the associated publication in any use of this plasmid: DOI: 10.1016/j.cell.2018.02.033

Terms and Licenses

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

Depositor Comments

This material is based upon work supported by the U. S. Department of Energy, Office of Science, through the Genomic Science Program, Office of Biological and Environmental Research, under the Secure Biosystems Design Initiative. Sandia National Laboratories is managed by National Technology and Engineering Solutions of Sandia, LLC., a wholly owned subsidiary of Honeywell International, Inc., for the U.S. Department of Energy under contract no. DE-NA-0003525.

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:

    pPBO.ACT001 was a gift from Joseph Schoeniger (Addgene plasmid # 182711 ; http://n2t.net/addgene:182711 ; RRID:Addgene_182711)
  • For your References section:

    CRISPR-RNAa: targeted activation of translation using dCas13 fusions to translation initiation factors. Otoupal PB, Cress BF, Doudna JA, Schoeniger JS. Nucleic Acids Res. 2022 Aug 11. pii: 6660959. doi: 10.1093/nar/gkac680. 10.1093/nar/gkac680 PubMed 35950485