Date published: 2026-7-11

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EF-2 CRISPR/Cas9 KO Plasmid (h): sc-401163

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Datasheets
  • Target species: human
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • EF-2 CRISPR/Cas9 Knockout (KO) Plasmid (h) is a pool of plasmids, each encoding Cas9 nuclease and a target-specific 20 nt guide RNA (gRNA) designed for maximum knockout efficiency using sequences derived from the GeCKO v2 library
  • gRNA sequences direct Cas9 to induce site-specific double-strand breaks (DSBs) in the EF-2 genomic locus, resulting in gene knockout through non-homologous end joining (NHEJ)
  • The puromycin resistance and RFP genes are flanked by LoxP sites, enabling removal of selection markers via Cre recombinase (Cre Vector: sc-418923) after establishing stable knockout cell lines
  • Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: EF-2 Antibody (C-9): sc-166415
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    EF-2 CRISPR/Cas9 KO Plasmid (h)

    sc-401163
    20 µg
    $397.00

    Overview

    Human EEF2 encodes elongation factor 2 (EF-2), a core component of the translation elongation cycle that drives ribosomal translocation on mRNA and sustains global protein synthesis. EF-2 activity is tightly coupled to nutrient and stress signaling through EF2K-mediated phosphorylation and intersects with mTOR-regulated translational control, linking ribosome dynamics to cellular growth and metabolic adaptation. Perturbation of EEF2 influences proteostasis, cell-cycle progression, and stress responses, and altered EF-2 regulation has been reported across contexts involving dysregulated proliferation and neurobiology. As a central node in translation control, EEF2 is routinely studied in pathways governing ribosome function, integrated stress signaling, and selective translation under stress.

    EF-2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the EEF2 gene in human 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.

    Key Features

    • sgRNAs targeting EEF2 exon(s) critical for EF-2 function
    • Co-expression of SpCas9 and sgRNA from a single plasmid for simplified delivery
    • GFP reporter for identification of transfected cells
    • Pool of plasmids targeting multiple EEF2 genomic sites to improve knockout efficiency
    • Compatible with delivery by transfection

    Design Variants

    CRISPRs +/- HDRs

    • gRNAs encoded by EF-2 CRISPR/Cas9 KO Plasmid (h) and EF-2 CRISPR/Cas9 KO Plasmid (h2) target distinct sites within the EEF2 locus. One or both targeting designs may be available. See Related Products for availability.
    • HDR donor constructs encoded by EF-2 HDR Plasmid (h) and EF-2 HDR Plasmid (h2) contain a puromycin resistance cassette and an RFP reporter flanked by EEF2 homology arms to support homology-directed repair at defined EEF2 target sites corresponding to the CRISPR/Cas9 KO designs. HDR donor availability may vary. See Related Products for availability.

    For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.