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Addgene

pT3TS-zSpRY
(Plasmid #179317)

Ordering

This material is available to academics and nonprofits only.
Item Catalog # Description Quantity Price (USD)
Plasmid 179317 Standard format: Plasmid sent in bacteria as agar stab 1 $85

Backbone

  • Vector backbone
    pT3TS
  • Backbone size w/o insert (bp) 3150
  • Total vector size (bp) 7330
  • Vector type
    CRISPR ; In vitro transcription by T3 promoter

Growth in Bacteria

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

Gene/Insert

  • Gene/Insert name
    Zebrafish codon-optimized Cas9 variant SpRY
  • Alt name
    SpRY
  • Species
    Synthetic
  • Insert Size (bp)
    4104
  • Mutation
    SpRY=A61R/L1111R/D1135L/S1136W/G1218K/E1219Q/ N1317R/A1322R/R1333P/R1335Q/T1337R
  • Tags / Fusion Proteins
    • SV40-NLS (N terminal on insert)
    • SV40-NLS (C terminal on insert)

Resource Information

  • Supplemental Documents
  • A portion of this plasmid was derived from a plasmid made by
    pT3TS_zCas9 (Addgene; 46757) (Jao et al., 2013) was modified by site-directed mutagenesis to generate this plasmid encoding the SpRY zebrafish codon-optimized variant

Terms and Licenses

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

Depositor Comments

This plasmid is owned by Moreno-Mateos Lab (CABD, Seville, Spain).

Please visit https://www.biorxiv.org/content/10.1101/2021.06.06.447255v2 for bioRxiv preprint.

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:

    pT3TS-zSpRY was a gift from Miguel Angel Moreno-Mateos (Addgene plasmid # 179317 ; http://n2t.net/addgene:179317 ; RRID:Addgene_179317)
  • For your References section:

    Genome editing in animals with minimal PAM CRISPR-Cas9 enzymes. Vicencio J, Sanchez-Bolanos C, Moreno-Sanchez I, Brena D, Vejnar CE, Kukhtar D, Ruiz-Lopez M, Cots-Ponjoan M, Rubio A, Melero NR, Crespo-Cuadrado J, Carolis C, Perez-Pulido AJ, Giraldez AJ, Kleinstiver BP, Ceron J, Moreno-Mateos MA. Nat Commun. 2022 May 12;13(1):2601. doi: 10.1038/s41467-022-30228-4. 10.1038/s41467-022-30228-4 PubMed 35552388