Date published: 2026-7-5

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PKC epsilon CRISPR/Cas9 KO Plasmid (m): sc-422261

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Datasheets
  • Target species: mouse
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • PKC epsilon CRISPR/Cas9 Knockout (KO) Plasmid (m) 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 PKC epsilon 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: PKC epsilon Antibody (E-5): sc-1681
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    PKC epsilon CRISPR/Cas9 KO Plasmid (m)

    sc-422261
    20 µg
    $397.00

    Overview

    Prkce encodes protein kinase C epsilon (PKCε), a diacylglycerol-responsive serine/threonine kinase that integrates signals from phospholipids and receptor-driven pathways to shape cell behavior. PKCε modulates phosphorylation networks controlling cytoskeletal remodeling, vesicle trafficking, and cell survival programs, and is commonly linked to MAPK/ERK and PI3K–AKT signaling outputs in multiple cell types. In mouse systems, Prkce activity is studied in the context of stress responses, inflammatory signaling, and tissue remodeling, where altered PKCε signaling can influence phenotypes relevant to metabolic and cardiovascular biology as well as tumor-associated processes. These functional connections make Prkce a useful node for dissecting kinase-driven pathway cross-talk and signal-dependent cellular plasticity.

    PKC epsilon CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Prkce gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Prkce 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 Prkce 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 PKC epsilon protein expression.

    This CRISPR knockout system enables efficient generation of Prkce-deficient cell models for investigation of PKC epsilon signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.

    Key Features

    • sgRNAs targeting Prkce exon(s) critical for PKC epsilon 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 Prkce genomic sites to improve knockout efficiency
    • Compatible with delivery by transfection

    Design Variants

    CRISPRs +/- HDRs

    • gRNAs encoded by PKC epsilon CRISPR/Cas9 KO Plasmid (m) and PKC epsilon CRISPR/Cas9 KO Plasmid (m2) target distinct sites within the Prkce locus. One or both targeting designs may be available. See Related Products for availability.
    • HDR donor constructs encoded by PKC epsilon HDR Plasmid (m) and PKC epsilon HDR Plasmid (m2) contain a puromycin resistance cassette and an RFP reporter flanked by Prkce homology arms to support homology-directed repair at defined Prkce 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.