
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
M-cadherin CRISPR/Cas9 KO Plasmid (h) | sc-401232 | 20 µg | $397.00 |
CDH15 encodes M-cadherin, a calcium-dependent cell–cell adhesion receptor enriched in skeletal muscle that supports myoblast recognition, alignment, and fusion during myogenesis and muscle regeneration. Through cadherin-mediated junctions and linkage to β-catenin/p120-catenin and the actin cytoskeleton, M-cadherin contributes to contact-dependent signaling that influences cytoskeletal remodeling, migration, and differentiation programs. CDH15 activity intersects with pathways governing adherens junction dynamics and can modulate cellular responses relevant to tissue repair and remodeling. Altered expression of cadherins, including CDH15, has been associated with changes in cell adhesion and invasive behavior in disease contexts, making it relevant for studies of tumor cell–cell interactions and muscle-associated pathophysiology.
M-cadherin CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CDH15 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CDH15 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 CDH15 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 M-cadherin protein expression.
This CRISPR knockout system enables efficient generation of CDH15-deficient cell models for investigation of M-cadherin 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.