Date published: 2026-8-28

1-800-457-3801

SCBT Portrait Logo
Seach Input

PDGF-B CRISPR/Cas9 KO Plasmid (h): sc-400586

0.0(0)
Write a reviewAsk a question

Datasheets
  • Target species: human
  • 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
  • PDGF-B 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 PDGF-B 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: PDGF-B Antibody (C-5): sc-74494
    Gene Editing Promo Banner

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    PDGF-B CRISPR/Cas9 KO Plasmid (h)

    sc-400586
    20 µg
    $397.00

    Overview

    PDGFB encodes platelet-derived growth factor subunit B (PDGF-B), a secreted mitogen that forms active PDGF dimers and signals primarily through PDGF receptor tyrosine kinases to regulate pericyte recruitment, vascular maturation, and mesenchymal cell proliferation. PDGF-B–driven signaling engages MAPK/ERK, PI3K–AKT, and PLCγ pathways, shaping cytoskeletal remodeling, chemotaxis, and extracellular matrix deposition in stromal and vascular compartments. Dysregulated PDGFB expression or PDGF axis activation is implicated in pathological angiogenesis, fibrotic remodeling, and PDGF-dependent autocrine or paracrine growth circuits observed across diverse tumor microenvironments. As a result, PDGFB is widely studied in endothelial–pericyte communication, wound repair biology, and stromal signaling networks relevant to tissue remodeling and cancer biology.

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

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

    Key Features

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

    Design Variants

    CRISPRs +/- HDRs

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