E-cadherin CRISPR/Cas9 KO Plasmid (canine): sc-437341
- Target species: canine
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- E-cadherin CRISPR/Cas9 Knockout (KO) Plasmid (canine) is a pool of plasmids, each encoding Cas9 nuclease and a target-specific 20 nt guide RNA (gRNA) designed for maximum knockout efficiency using sequences derived from the GeCKO v2 library
- gRNA sequences direct Cas9 to induce site-specific double-strand breaks (DSBs) in the E-cadherin genomic locus, resulting in gene knockout through non-homologous end joining (NHEJ)
- The puromycin resistance and RFP genes are flanked by LoxP sites, enabling removal of selection markers via Cre recombinase (Cre Vector: sc-418923) after establishing stable knockout cell lines
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
E-cadherin CRISPR/Cas9 KO Plasmid (canine) | sc-437341 | 20 µg | $397.00 |
Overview
E-cadherin (CDH1) is a calcium-dependent cell–cell adhesion glycoprotein that mediates adherens junction formation and epithelial tissue integrity in canine cells. Through its cytoplasmic association with catenins, E-cadherin connects to the actin cytoskeleton and regulates epithelial polarity, contact inhibition, and barrier function. Loss or dysregulation of E-cadherin perturbs junctional signaling and can promote epithelial-to-mesenchymal transition (EMT) programs, with downstream effects on Wnt/β-catenin signaling, migration, and invasion-related phenotypes. Altered E-cadherin expression and junctional architecture are commonly studied in the context of tumor progression, fibrosis, and inflammatory remodeling in epithelial tissues.
E-cadherin CRISPR/Cas9 KO Plasmid (canine) is a pool of plasmids designed for targeted disruption of the gene in canine cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the 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 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 E-cadherin protein expression.
This CRISPR knockout system enables efficient generation of -deficient cell models for investigation of E-cadherin signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
Key Features
- sgRNAs targeting exon(s) critical for E-cadherin function
- Co-expression of SpCas9 and sgRNA from a single plasmid for simplified delivery
- GFP reporter for identification of transfected cells
- Pool of plasmids targeting multiple genomic sites to improve knockout efficiency
- Compatible with delivery by transfection
Design Variants
CRISPRs +/- HDRs
- gRNAs encoded by E-cadherin CRISPR/Cas9 KO Plasmid (canine) and E-cadherin CRISPR/Cas9 KO Plasmid (canine2) target distinct sites within the locus. One or both targeting designs may be available. See Related Products for availability.
- HDR donor constructs encoded by E-cadherin HDR Plasmid (canine) and E-cadherin HDR Plasmid (canine2) contain a puromycin resistance cassette and an RFP reporter flanked by homology arms to support homology-directed repair at defined target sites corresponding to the CRISPR/Cas9 KO designs. HDR donor availability may vary. See Related Products for availability.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.