
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
NEPH3 CRISPR/Cas9 KO Plasmid (h) | sc-406190 | 20 µg | $397.00 |
KIRREL2 encodes NEPH3, an immunoglobulin superfamily adhesion molecule enriched at specialized cell–cell junctions where it supports formation and maintenance of slit diaphragm–like structures and epithelial barrier organization. NEPH3 participates in contact-dependent signaling and cytoskeletal remodeling through interactions with scaffold proteins that coordinate actin dynamics and junctional complex stability. In kidney-relevant contexts, NEPH3-associated complexes are linked to podocyte architecture, filtration barrier integrity, and cellular responses to mechanical or inflammatory stress. Dysregulation of NEPH family adhesion networks has been associated with glomerular pathology and altered epithelial differentiation, making KIRREL2 a useful target for studying junctional signaling and tissue homeostasis.
NEPH3 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the KIRREL2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the KIRREL2 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 KIRREL2 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 NEPH3 protein expression.
This CRISPR knockout system enables efficient generation of KIRREL2-deficient cell models for investigation of NEPH3 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.