You are here: Home > Products > Genome editing tools >

CRISPR human sgRNA libraries

Introduction

GeneCopoeia offers CRISPR sgRNA libraries for high-throughput knockout of human genes in specific or custom gene groups or pathways. Loss-of-function screening by gene knockout is a powerful tool for systematic genetic analysis in mammalian cells, facilitating gene discovery, genome-scale functional interrogation (e.g. signal transduction pathways) and drug discovery (e.g. target identification and drug mechanism studies).

The Genome-CRISP™ human single guide RNA (sgRNA) libraries are cloned into lentiviral vectors for dual-use (transfection or transduction) delivery methods designed for large-scale functional screens. For each targeted gene, a minimum of 2 barcoded sgRNAs targeting different regions are created, optimized and sequence-verified to ensure efficient gene knockout. Further, each sgRNA-expressing plasmid is individually cultured in E. coli before pooling, providing the best possible representation of each sgRNA in the pools. The libraries can be ordered as pools of sgRNAs in pre-defined gene families or as custom sets, and are available as lentiviral particles, transfection-ready plasmid DNA or bacterial stocks. They can be transfected or transduced into cell lines, including those stably expressing Cas9 nuclease.
 

Illustration-of-CRISPR_Cas9-mediated-genome-editing

 

Figure 1. Illustration of large scale screening with sgRNA library

 

 

Applications

Applications

  • High-throughput knockout screening with many sgRNAs, either individually or in pools.
  • Drug target discovery (Figure 2).
  • Drug target validation.
  • Phenotypic screens.
  • Reporter assays.

 

 

 

Figure 2. Workfow for CRISPR sgRNA libraries. A. Pooled screen. Cells infected with each sgRNA library pool are screened for the desired readout. Pooled cells are subjected to Sanger sequencing for individual sgRNAs, or deep sequencing to look for over- or under-representation of individual sgRNAs. B. Knockout screen using arrayed sgRNAs. Cells are infected with individual sgRNA lentiviruses. Wells are screened for the readout of interest. Individual sgRNAs corresponding to the phenotype of interest are already known without sequencing.

 

 

To order

The Genome-CRISP™ CRISPR human sgRNA libraries consist of sequence-verified sgRNA target sites cloned into a lentiviral vector. The clones do not carry the Cas9 nuclease. You will need to either purchase a lentiviral Cas9 clone or a cell line stably expressing Cas9. For lentiviral transduction, we recommend using a cell line stably expressing Cas9 before transduction with the libraries.

Human sgRNA libraries

   
 

Choose your delivery format to display price*:

   

 

Buy Catalog number Library name Number of sgRNAs Number of genes Number of tubes Vector Price*
L01-LS03 sgRNA library: Innate kinases & ubiquitin ligases 475 239 4 tubes, 118-119 sgRNAs each pCRISPR-LvSG03 Choose format
L02-LS03 sgRNA library: Nuclear hormone receptors 236 118 2 tubes, 118 sgRNAs each pCRISPR-LvSG03 Choose format
L03-LS03 sgRNA library: Tumor metastasis genes 114 57 2 tubes, 57 sgRNAs each pCRISPR-LvSG03 Choose format
L04-LS03 sgRNA library: Oncogenes 576 288 4 tubes, 144 sgRNAs each pCRISPR-LvSG03 Choose format
L05-LS03 sgRNA library: Tumor suppressor genes 462 231 4 tubes, 115-116 sgRNAs each pCRISPR-LvSG03 Choose format
L06-LS03 sgRNA library: Protein kinases 1,316 658 10 tubes, 131-132 sgRNAs each pCRISPR-LvSG03 Choose format
L07-LS03 sgRNA library: Key genes in 50 pathways 278 139 2 tubes, 139 sgRNAs each pCRISPR-LvSG03 Choose format

Custom sgRNA libraries also available upon request. Contact us for a quote.

*Prices are for academic and government customers only. Industry customers, please contact us for a quote.

 


 

Cas9 clones, lentiviral particles, and stable cell lines

Buy Catalog# Product Price
Cas9 clones
CP-LvC9NU-01 Cas9 nuclease lentiviral expression clone $595
CP-LvC9NU-02 Cas9 nuclease lentiviral expression clone $595
CP-LvC9NU-09 Cas9 nuclease lentiviral expression clone $595
CP-LvC9NU-10 Cas9 nuclease lentiviral expression clone $595

Custom Cas9-expressing stable cell lines also available upon request. Contact us for a quote.


 

Premade Cas9 clones lentiviral particles

Buy Catalog Product Name Description Price
LPP-CP-LvC9NU-01-100-C Cas9 Nuclease Purified Lentifect™ Lentiviral Particles (100 µl x 1 vial) >1x107 TU/ml Cas9 nuclease lentiviral particles ready for transduction,100 µl (CMV/Neomycin) $725
LPP-CP-LvC9NU-02-100-C Cas9 Nuclease Purified Lentifect™ Lentiviral Particles (100 µl x 1 vial) > 1x107 TU/ml Cas9 nuclease lentiviral particles ready for transduction,100 µl (CMV/eGFP/Neomycin) $725
LPP-CP-LvC9NU-08-100-C Cas9 Nuclease Purified Lentifect™ Lentiviral Particles (100 µl x 1 vial) > 1x107 TU/ml Cas9 nuclease lentiviral particles ready for transduction,100 µl (EF1α/Puromycin) $725
LPP-CP-LvC9NU-09-100-C Cas9 Nuclease Purified Lentifect™ Lentiviral Particles (100 µl x 1 vial) > 1x107 TU/ml Cas9 nuclease lentiviral particles ready for transduction,100 µl (EF1α/eGFP/Neomycin) $725
LPP-CP-LvC9NU-10-100-C Cas9 Nuclease Purified Lentifect™ Lentiviral Particles (100 µl x 1 vial) > 1x107 TU/ml Cas9 nuclease lentiviral particles ready for transduction,100 µl (EF1α/eGFP/Hygromycin) $725

 

 

 

 

Resources

FAQs

Answer: Lentiviral particles, transfection-ready DNA, and bacterial stock.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Answer: Yes. Currently, our sgRNA libraries are available standard as pools. However, if you wish to receive your libraries as individually arrayed clones, simply contact us for a custom quote.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Answer: Yes. However, we strongly recommend that you first establish a cell line that is stably expressing Cas9, in order to best maintain consistent representation of each sgRNA in the library. First, transduce your cells with the Cas9 lentiviral clone. Once you have established the stable Cas9-expressing cell line, use the sgRNA libraries for transduction.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Answer: You can't completely ensure that every cell is infected with one sgRNA, or that all sgRNAs are represented in the pool of infected cells. However, these libraries are small, so if the number of infected cells was 100 × the number of sgRNAs in the library, then you should have close to complete representation. 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Answer: Yes. The lentiviral plasmids are "dual-use", so that they can either be packaged into lentiviral particles or transfected into cells by standard transfection methods.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Technical Note

Genome Editing: Applications For GeneCopoeia CRISPR sgRNA Libraries

 

User Manual

Genome-CRISP™ human sgRNA Library User Manual

 

References

  • Shalem, et al. (2014). Genome-scale CRISPR-Cas9 knockout screening in human cells. Science 343, 84.
  • Wang, et al. (2014). Genetic screens in human cells using the CRISPR-Cas9 system. Science 343, 80.
  • Zhou, et al. (2014). High-throughput screening of a CRISPR/Cas9 library for functional genomics in human cells. Nature 509, 487.