
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
HoxA3 CRISPR/Cas9 KO Plasmid (h) | sc-404634 | 20 µg | $397.00 |
HOXA3 encodes the homeobox transcription factor HoxA3, a sequence-specific DNA-binding regulator that patterns anterior–posterior identity during embryogenesis and coordinates programs governing morphogenesis, epithelial differentiation, and tissue remodeling. HoxA3 integrates with HOX cluster regulatory networks and intersects with developmental signaling pathways such as WNT, BMP/TGF-β, and retinoic acid to shape cell fate decisions and spatial gene expression. In adult contexts, altered HOXA3 expression or epigenetic dysregulation has been linked to aberrant differentiation states and transcriptional rewiring observed in cancer and other disorders involving developmental gene reactivation. As a nuclear regulator, HoxA3 is frequently studied in gene regulatory network mapping, lineage specification models, and chromatin-mediated control of transcription.
HoxA3 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the HOXA3 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the HOXA3 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 HOXA3 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 HoxA3 protein expression.
This CRISPR knockout system enables efficient generation of HOXA3-deficient cell models for investigation of HoxA3 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.