Focused Ras Synthetic Lethal Human CRISPR Knockout Library
(Pooled Library #92352)
-
Purpose
The Sabatini/Lander CRISPR pooled library is a focused gRNA library that targets synthetic lethal candidate and control genes with oncogenic Ras.
-
Vector Backbone
lentiCRISPR v1 (Plasmid #49535) - expresses Cas9
Note: This plasmid has been discontinued, as an updated version is available. For confirmation of screen hits, Addgene encourages users to use the updated lentiCRISPR v2 (Plasmid #52961), which can be requested separately.
-
Depositing Labs
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |||
---|---|---|---|---|---|---|---|
Pooled Library | 92352 | gRNA library in lentiCRISPR v1 | 1 | $275 | Add to Cart |
Library Details
-
SpeciesHuman
-
Genes targeted132
-
gRNAs6,661
-
Controls499 intergenic
-
Lentiviral Generation3rd
Library Shipping
Each library is delivered in a microcentrifuge tube on blue ice. The tube's contents will not necessarily be frozen. For best results, minimize freeze/thaws.
-
Volume∼10 µL
-
Concentration10 ng/µL
Resource Information
-
Protocols
-
Depositor Data
-
Terms and Licenses
Academic/Nonprofit TermsIndustry Terms- Not Available to Industry
Trademarks- Zeocin® is an InvivoGen trademark.
Depositor Comments
When performing sgRNA validation in a Cas9-expressing cell line, the depositing laboratory recommends using plasmid pLenti-sgRNA (Addgene #71049).
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:
Focused Ras Synthetic Lethal Human CRISPR Knockout Library was a gift from David Sabatini and Eric Lander (Addgene #92352) -
For your References section:
Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras. Wang T, Yu H, Hughes NW, Liu B, Kendirli A, Klein K, Chen WW, Lander ES, Sabatini DM. Cell. 2017 Feb 1. pii: S0092-8674(17)30061-2. doi: 10.1016/j.cell.2017.01.013. PubMed 28162770