
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
EF-2 CRISPR/Cas9 KO Plasmid (m) | sc-420117 | 20 µg | $397.00 |
Eef2 encodes eukaryotic elongation factor 2 (EF-2), a conserved GTPase that drives ribosomal translocation during mRNA translation elongation and thereby controls global protein synthesis rates. EF-2 activity is tightly regulated by phosphorylation via eEF2 kinase downstream of nutrient- and stress-sensing pathways, including mTOR signaling, linking translational output to energy status, hypoxia, and synaptic activity. Through its central role in proteostasis, EF-2 influences cell growth, stress responses, and differentiation programs that depend on rapid remodeling of the proteome. Dysregulated translational control involving EF-2 and eEF2K has been implicated in neurological dysfunction and tumor-associated metabolic adaptation, making Eef2 a useful node for mechanistic studies of translational regulation in mouse systems.
EF-2 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Eef2 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Eef2 together with the Streptococcus pyogenes Cas9 nuclease. The plasmids also encode GFP, allowing fluorescent identification and enrichment of successfully transfected cells by fluorescence microscopy or flow cytometry.
The multi-guide design increases the likelihood of generating insertions or deletions (indels) that disrupt the Eef2 open reading frame following Cas9-mediated double-strand break formation. DNA breaks introduced by the CRISPR/Cas9 system are repaired through endogenous non-homologous end joining (NHEJ) pathways, frequently resulting in frameshift mutations that abolish EF-2 protein expression.
This CRISPR knockout system enables efficient generation of Eef2-deficient cell models for investigation of EF-2 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.