
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
FOXC2 CRISPR/Cas9 KO Plasmid (m) | sc-420370 | 20 µg | $397.00 |
Foxc2 encodes the forkhead box transcription factor FOXC2, a DNA-binding regulator that coordinates gene expression programs controlling mesenchymal cell identity, vascular and lymphatic development, and adipose tissue remodeling in mouse. FOXC2 functions within nucleus-driven transcriptional networks that intersect with developmental signaling pathways such as TGF-β and Notch to influence endothelial differentiation, extracellular matrix organization, and epithelial–mesenchymal transition–like processes. Altered FOXC2 activity has been linked to dysregulated lymphangiogenesis, aberrant vascular patterning, and shifts in metabolic and stromal states that are commonly investigated in models of developmental disorders and tumor microenvironment biology. These roles make Foxc2 a useful node for dissecting transcriptional control of tissue morphogenesis and cell fate decisions.
FOXC2 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Foxc2 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Foxc2 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 Foxc2 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 FOXC2 protein expression.
This CRISPR knockout system enables efficient generation of Foxc2-deficient cell models for investigation of FOXC2 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.