
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
ADAM15 CRISPR/Cas9 KO Plasmid (h) | sc-405627 | 20 µg | $397.00 |
ADAM15 encodes a transmembrane metalloprotease-disintegrin that participates in ectodomain shedding and cell–cell/cell–matrix interactions through its protease, disintegrin, and cytoplasmic domains. It modulates signaling networks linked to adhesion and motility, including integrin-associated pathways, and can influence availability of membrane-tethered ligands and receptors via regulated proteolysis. ADAM15 activity has been connected to processes such as migration, invasion, and inflammatory signaling, and altered expression has been reported across multiple disease contexts including cancer progression and vascular pathology. As a surface-associated protease, ADAM15 is frequently studied for its contributions to extracellular remodeling and signal transduction crosstalk at the plasma membrane.
ADAM15 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the ADAM15 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the ADAM15 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 ADAM15 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 ADAM15 protein expression.
This CRISPR knockout system enables efficient generation of ADAM15-deficient cell models for investigation of ADAM15 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.