
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
caveolin-3 CRISPR/Cas9 KO Plasmid (h) | sc-400569 | 20 µg | $397.00 |
CAV3 encodes caveolin-3, a muscle-enriched structural component of caveolae that organizes membrane microdomains and scaffolds signaling complexes at the sarcolemma. Caveolin-3 contributes to mechanoprotection and membrane trafficking and modulates pathways involving GPCR signaling, insulin receptor signaling, ion channel regulation, and nitric oxide signaling through compartmentalization of receptors and kinases. In striated muscle, it supports T-tubule organization, excitation–contraction coupling, and stability of the dystrophin-associated protein complex. Altered CAV3 function or expression is associated with caveolinopathies affecting skeletal and cardiac muscle, including dystrophic phenotypes, cardiomyopathy, and arrhythmia-related mechanisms, making it relevant for studies of membrane signaling and muscle integrity.
caveolin-3 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CAV3 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CAV3 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 CAV3 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 caveolin-3 protein expression.
This CRISPR knockout system enables efficient generation of CAV3-deficient cell models for investigation of caveolin-3 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.