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Addgene

lenti SYN-dCas9-KRAB-MeCP2
(Plasmid #155365)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 155365 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    lentiCRISPR v2
  • Backbone manufacturer
    Feng Zhang Addgene plasmid #52961
  • Backbone size w/o insert (bp) 7958
  • Total vector size (bp) 13451
  • Vector type
    Mammalian Expression, Lentiviral, CRISPR

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    dCas9-KRAB-MeCP2
  • Species
    Synthetic
  • Insert Size (bp)
    5445
  • Promoter SYN
  • Tags / Fusion Proteins
    • 3x FLAG (N terminal on insert)
    • 7x His (C terminal on insert)

Cloning Information

Resource Information

  • Supplemental Documents
  • A portion of this plasmid was derived from a plasmid made by
    dCas9-KRAB-MeCP2 was a gift from Alejandro Chavez & George Church (Addgene plasmid # 110821 ; http://n2t.net/addgene:110821 ; RRID:Addgene_110821)
  • Articles Citing this Plasmid

Terms and Licenses

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

Depositor Comments

Full cloning information and validation can be found in preprint on BioRxiv. doi: https://doi.org/10.1101/2020.05.26.116822
https://www.biorxiv.org/content/10.1101/2020.05.26.116822v1

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:

    lenti SYN-dCas9-KRAB-MeCP2 was a gift from Jeremy Day (Addgene plasmid # 155365 ; http://n2t.net/addgene:155365 ; RRID:Addgene_155365)
  • For your References section:

    An Improved CRISPR/dCas9 Interference Tool for Neuronal Gene Suppression. Duke CG, Bach SV, Revanna JS, Sultan FA, Southern NT, Davis MN, Carullo NVN, Bauman AJ, Phillips RA 3rd, Day JJ. Front Genome Ed. 2020 Sep 15;2:9. doi: 10.3389/fgeed.2020.00009. eCollection 2020. 10.3389/fgeed.2020.00009 PubMed 34713218