Date published: 2026-7-10

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PP2A-Cβ CRISPR/Cas9 KO Plasmid (m): sc-422382

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Datasheets
  • Target species: mouse
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • PP2A-Cβ 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 PP2A-Cβ 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: PP2A-Cα/β Antibody (1D6): sc-80665
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    PP2A-Cβ CRISPR/Cas9 KO Plasmid (m)

    sc-422382
    20 µg
    $397.00

    Overview

    Ppp2cb encodes the catalytic Cβ subunit of protein phosphatase 2A (PP2A), a major serine/threonine phosphatase that counterbalances kinase signaling by dephosphorylating diverse substrates in the cytoplasm and nucleus. PP2A-Cβ-containing holoenzymes regulate cell-cycle progression, DNA damage responses, apoptosis, and metabolic control through pathways that include PI3K–AKT, MAPK/ERK, and Wnt/β-catenin signaling. In mouse systems, perturbation of PP2A activity influences phosphorylation homeostasis and can reshape signaling networks that are frequently implicated in oncogenic transformation and neurobiological dysfunction. Ppp2cb therefore serves as a useful node for dissecting phosphatase-dependent control of growth, stress adaptation, and neuronal signaling.

    PP2A-Cβ CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Ppp2cb gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Ppp2cb 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 Ppp2cb 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 PP2A-Cβ protein expression.

    This CRISPR knockout system enables efficient generation of Ppp2cb-deficient cell models for investigation of PP2A-Cβ signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.

    Key Features

    • sgRNAs targeting Ppp2cb exon(s) critical for PP2A-Cβ 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 Ppp2cb genomic sites to improve knockout efficiency
    • Compatible with delivery by transfection

    Design Variants

    CRISPRs +/- HDRs

    • gRNAs encoded by PP2A-Cβ CRISPR/Cas9 KO Plasmid (m) and PP2A-Cβ CRISPR/Cas9 KO Plasmid (m2) target distinct sites within the Ppp2cb locus. One or both targeting designs may be available. See Related Products for availability.
    • HDR donor constructs encoded by PP2A-Cβ HDR Plasmid (m) and PP2A-Cβ HDR Plasmid (m2) contain a puromycin resistance cassette and an RFP reporter flanked by Ppp2cb homology arms to support homology-directed repair at defined Ppp2cb 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.