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Chen Mouse Tumor Suppressor Gene CRISPR Knockout Library
(Pooled Libraries #113584, #113585)

  • Purpose

    This AAV CRISPR knockout library targets mouse tumor suppressor genes (TSG). Each plasmid carries one TSG-targeting sgRNA in addition to one p53-targeting sgRNA. Because the backbone expresses both luciferase and Cre, the library can be used to interrogate tumorigenesis in vivo using a mouse line expressing Cre-dependent Cas9.

  • Vector Backbone

    EFS-Vector and TBG-Vector - do not express Cas9; Luciferase and Cre are driven by EF1-alpha and TBG promoters, respectively


Item Catalog # Description Quantity Price (USD)
Pooled Library 113584 mTSG CRISPR Knockout Library - EF1-alpha promoter 1 $ 275 Add to Cart
Pooled Library 113585 mTSG CRISPR Knockout Library - TBG promoter 1 $ 275 Add to Cart
Available to Academic and Nonprofits Only

  • A Cas9 plasmid is NOT included with this item. Can be used with other plasmid(s) or cell lines expressing Cas9 or in vivo with LSL-Cas9 transgenic mice.

Library Details

  • Species
  • Genes targeted
  • gRNAs
  • Controls
  • Virus Type

Library Shipping

This library is delivered as suspended DNA in a microcentrifuge tube on blue ice. The tube's contents will not necessarily be frozen. For best results, minimize freeze-thaws.

  • Volume
    ∼20 µL
  • Concentration
    50 ng/µL
How to cite this pooled library ( Back to top )

These pooled libraries 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:

    Mouse Tumor Suppressor Gene CRISPR Knockout Library was a gift from Sidi Chen (Addgene # )
  • For your References section:

    Mapping a functional cancer genome atlas of tumor suppressors in mouse liver using AAV-CRISPR-mediated direct in vivo screening. Wang G, Chow RD, Ye L, Guzman CD, Dai X, Dong MB, Zhang F, Sharp PA, Platt RJ, Chen S. Sci Adv. 2018 Feb 28;4(2):eaao5508. doi: 10.1126/sciadv.aao5508. eCollection 2018 Feb. PubMed 29503867