Date published: 2026-8-3

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PACAP CRISPR/Cas9 KO Plasmid (r): sc-437378

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Datasheets
  • Target species: rat
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • PACAP CRISPR/Cas9 Knockout (KO) Plasmid (r) 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 PACAP 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: PACAP Antibody (F-2): sc-166180
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    PACAP CRISPR/Cas9 KO Plasmid (r)

    sc-437378
    20 µg
    $397.00

    Overview

    Pituitary adenylate cyclase-activating polypeptide (PACAP; Adcyap1) is a conserved neuropeptide that signals primarily through the PAC1 receptor and can also engage VPAC receptors to regulate cAMP/PKA and MAPK/ERK-dependent transcription. In rat nervous and neuroendocrine systems, PACAP modulates neuronal excitability, neurotransmitter release, stress-axis signaling, and developmental programs including neurite outgrowth and cell survival. PACAP-driven signaling intersects with calcium homeostasis, synaptic plasticity, and inflammatory mediator regulation, linking this pathway to mechanisms relevant to pain processing, stress-related behaviors, and neuroinflammation. Dysregulated PACAP activity has been associated with altered autonomic and metabolic control and has been investigated in models of migraine-like phenotypes and neurodegenerative vulnerability.

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

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

    Key Features

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

    Design Variants

    CRISPRs +/- HDRs

    • gRNAs encoded by PACAP CRISPR/Cas9 KO Plasmid (r) and PACAP CRISPR/Cas9 KO Plasmid (r2) target distinct sites within the locus. One or both targeting designs may be available. See Related Products for availability.
    • HDR donor constructs encoded by PACAP HDR Plasmid (r) and PACAP HDR Plasmid (r2) contain a puromycin resistance cassette and an RFP reporter flanked by homology arms to support homology-directed repair at defined 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.