
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
CD362/SDC2/Syndecan-2 CRISPR/Cas9 KO Plasmid (m) | sc-420985 | 20 µg | $397.00 |
Sdc2 encodes syndecan-2 (CD362/SDC2), a transmembrane heparan sulfate proteoglycan that functions as a co-receptor for extracellular matrix components and heparin-binding growth factors. By organizing cell-surface proteoglycan–ligand interactions, SDC2 regulates cell adhesion, migration, and cytoskeletal remodeling and influences signaling through pathways such as FGF, VEGF, Wnt, and integrin/FAK–SRC networks. In mouse systems, Sdc2 has been used to study stromal–epithelial communication, angiogenic responses, and tissue remodeling in development and injury models. Altered SDC2 expression or glycosylation is also investigated in contexts of fibrosis and tumor microenvironment biology, where matrix-dependent signaling can modulate proliferation and invasiveness.
CD362/SDC2/Syndecan-2 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Sdc2 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Sdc2 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 Sdc2 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 CD362/SDC2/Syndecan-2 protein expression.
This CRISPR knockout system enables efficient generation of Sdc2-deficient cell models for investigation of CD362/SDC2/Syndecan-2 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.