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Addgene

Human Genome-Wide Reduced Double-gRNA Library
(Pooled Library #137999)

  • Purpose

    This lentiviral CRISPR knockout library enables genome-wide screens in human cell lines at reduced scale. Through optimization of guide RNA designs and delivery of two gRNAs with each construct a five-fold reduction in size is achieved without impacting performance compared with a sgRNA library with five gRNAs per target.

  • Vector Backbone

Ordering

Item Catalog # Description Quantity Price (USD)
Pooled Library 137999 Human Genome-Wide Reduced Double-gRNA Library 1 $540 Add to Cart
Available to Academic and Nonprofits Only
  • A Cas9 plasmid is NOT included with this item and will have to be ordered separately. Can be used in conjunction with pKLV2-EF1a-Cas9Bsd-W (Addgene #68343) or other plasmids or cell lines expressing Cas9.

Library Details

  • Species
    Human
  • Genes targeted
    19,657
  • gRNAs
    59,576
  • Controls
    398 non-targeting controls
  • Lentiviral Generation
    3rd

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

Resource Information

Depositor Comments

Please visit https://www.biorxiv.org/content/10.1101/859652v1 (Link opens in a new window) for bioRxiv preprint.

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:

    Human Reduced Double-gRNA Library was a gift from Leopold Parts (Addgene #137999)
  • For your References section:

    Minimized double guide RNA libraries enable scale-limited CRISPR/Cas9 screens. Peets EM, Crepaldi L, Zhou Y, Allen F, Elmentaite R, Noell G, Turner G, Iyer V, Parts L. bioRxiv 859652. doi: 10.1101/859652. bioRxiv 859652