
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
claudin-1 CRISPR/Cas9 KO Plasmid (h) | sc-400609 | 20 µg | $397.00 |
CLDN1 encodes claudin-1, an integral membrane component of tight junction strands that regulates epithelial barrier integrity, paracellular permeability, and apico-basal polarity. Claudin-1 participates in junctional organization and signaling through interactions with scaffold proteins such as ZO-1, influencing cytoskeletal dynamics and pathways linked to epithelial homeostasis, including Wnt/β-catenin and EMT-associated programs. Altered CLDN1 expression or localization is associated with barrier dysfunction and inflammatory processes, and it is frequently studied in contexts of epithelial transformation, invasion, and metastasis in multiple carcinomas. As a junctional determinant, claudin-1 is widely used as a marker and mechanistic node for interrogating adhesion-dependent signaling and tissue architecture.
claudin-1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CLDN1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CLDN1 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 CLDN1 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 claudin-1 protein expression.
This CRISPR knockout system enables efficient generation of CLDN1-deficient cell models for investigation of claudin-1 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.