CRISPR Activation & Repression

CRISPR Activation (CRISPRa) allows for gene specific up-regulation by using dCas9-SAM. This fusion protein consists of the catalytically dead Cas9 (dCas9) enzymefused to the Synergistic Activation Mediator (SAM). sgRNAs are designed to target and guide dCas9-SAM to the upstream promoter 5' UTR region of a specific gene thereby resulting in transcriptional up-regulation. 

Search Activation sgRNA Library

For gene activation, search for your gene of interest either by Gene Name or Accession Number:

Key Features

  • Comprehensive collection of gene activation sgRNAs
  • Targets include all human, mouse and rat genes.
  • Available in a set of 3 sgRNA vectors/viruses for added assurance of efficient gene activation
  • Lentiviral delivery results in host integration of DNA, leading to long term gene expression
  • Lentiviral vectors can be transfected for non-integrating, transient sgRNA expression

Looking for constructs expressing multiple sgRNAs? Check out our Custom Multiplex sgRNA Service.  

For Custom Activation/Repression sgRNAs, order here.  

Product Information

  • pLenti-U6-sgRNA-PGK-Neo vector map
    Vector Map
    sgRNA for activation of your gene of interest is available in lentiviral vector or lentivirus format.
  • CRISPR dCas9 SAM Lentivector Lentivirus Workflow
    Workflow
    How to use abm's activation sgRNA lentiviruses in your CRISPR activation experiment.
  • CRISPR Activation and Repression Knowledge Base
    Need Help Getting Started?
    Read our CRISPR Activation and Repression Knowledge Base article for more information.

Top Publications

Regulation of NKT cell-mediated immune responses to tumours and liver inflammation by mitochondrial PGAM5-Drp1 signalling.

Kang, Y J et al.
Nat. Commun. 6:8371 (2015).


DOI: 10.1038/ncomms9371.

Leukocyte cell-derived chemotaxin 2 is an antiviral regulator acting through the proto-oncogene MET.

Shirasaki, T. et al.
Nature Communications. (2022).


doi: 10.1038/s41467-022-30879-3

Clinical significance of SNORA42 as an oncogene and a prognostic biomarker in colorectal cancer.

Okugawa, Y et al.
Gut (2015)


doi:10.1136/gutjnl-2015-309359