Date published: 2026-7-10

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Agrin CRISPR/Cas9 KO Plasmid (h): sc-401256

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Datasheets
  • Target species: human
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • Agrin 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 Agrin 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: Agrin Antibody (D-2): sc-374117
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    Agrin CRISPR/Cas9 KO Plasmid (h)

    sc-401256
    20 µg
    $397.00

    Overview

    AGRN encodes agrin, a large heparan sulfate proteoglycan of the extracellular matrix that organizes cell–matrix signaling and membrane specialization. In neuromuscular and neuronal contexts, agrin coordinates synapse formation and stabilization by engaging receptors such as LRP4 and activating MuSK-dependent signaling, supporting acetylcholine receptor clustering and synaptic maturation. Beyond synaptogenesis, agrin influences cytoskeletal remodeling, adhesion, and mechanotransduction through interactions with dystroglycan and integrins, shaping tissue architecture. Dysregulated AGRN expression or processing has been associated with neuromuscular junction defects and altered synaptic homeostasis, and is also studied in pathways linked to fibrosis, neurodegeneration, and tumor microenvironment remodeling.

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

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

    Key Features

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

    Design Variants

    CRISPRs +/- HDRs

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