Date published: 2026-7-13

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USF-2 CRISPR/Cas9 KO Plasmid (h): sc-401713

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Datasheets
  • Target species: human
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • USF-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 USF-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: USF-2 Antibody (5E9): sc-293443
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    USF-2 CRISPR/Cas9 KO Plasmid (h)

    sc-401713
    20 µg
    $397.00

    Overview

    USF2 encodes upstream stimulatory factor 2 (USF-2), a ubiquitous bHLH-leucine zipper transcription factor that binds E-box motifs and modulates basal and stimulus-responsive gene expression. USF-2 participates in transcriptional control of metabolic homeostasis, cell-cycle progression, differentiation, and stress responses through coordinated regulation of promoter architecture and chromatin context. Its activity intersects with pathways governing glucose and lipid metabolism, inflammatory signaling, and oxidative stress, and it can influence transcriptional programs linked to tumor biology. Altered USF2 expression or function has been associated with dysregulated proliferation and metabolic phenotypes, making it a useful node for mechanistic studies of transcriptional network remodeling.

    USF-2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the USF2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the USF2 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 USF2 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 USF-2 protein expression.

    This CRISPR knockout system enables efficient generation of USF2-deficient cell models for investigation of USF-2 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.

    Key Features

    • sgRNAs targeting USF2 exon(s) critical for USF-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 USF2 genomic sites to improve knockout efficiency
    • Compatible with delivery by transfection

    Design Variants

    CRISPRs +/- HDRs

    • gRNAs encoded by USF-2 CRISPR/Cas9 KO Plasmid (h) and USF-2 CRISPR/Cas9 KO Plasmid (h2) target distinct sites within the USF2 locus. One or both targeting designs may be available. See Related Products for availability.
    • HDR donor constructs encoded by USF-2 HDR Plasmid (h) and USF-2 HDR Plasmid (h2) contain a puromycin resistance cassette and an RFP reporter flanked by USF2 homology arms to support homology-directed repair at defined USF2 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.