Date published: 2026-7-4

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aggrecan CRISPR/Cas9 KO Plasmid (h): sc-400760

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Datasheets
  • Target species: human
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • aggrecan 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 aggrecan 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: aggrecan Antibody (4F4): sc-33695
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    aggrecan CRISPR/Cas9 KO Plasmid (h)

    sc-400760
    20 µg
    $397.00

    Overview

    ACAN encodes aggrecan, a large chondroitin sulfate proteoglycan that forms the hydrated backbone of cartilage extracellular matrix by binding hyaluronan and link protein, enabling resistance to compressive load. Aggrecan turnover is coordinated by chondrocyte anabolic programs and catabolic extracellular proteolysis, including cleavage by ADAMTS aggrecanases and matrix remodeling pathways that shape tissue biomechanics. Perturbation of ACAN expression or aggrecan processing disrupts cartilage homeostasis and is implicated in degenerative and developmental skeletal phenotypes, making it a key node for studying extracellular matrix organization and mechanobiology. ACAN is therefore widely used as a marker and functional determinant in chondrocyte differentiation, growth plate biology, and cartilage matrix assembly studies.

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

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

    Key Features

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

    Design Variants

    CRISPRs +/- HDRs

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