
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
GRHL3 CRISPR/Cas9 KO Plasmid (h) | sc-404946 | 20 µg | $397.00 |
GRHL3 (grainyhead-like transcription factor 3) is a sequence-specific transcriptional regulator that coordinates epithelial differentiation, barrier formation, and wound-responsive gene programs. It helps maintain epidermal homeostasis by modulating keratinocyte proliferation and terminal differentiation networks and intersects with pathways controlling cell polarity, adhesion, and transcriptional control of structural and junctional genes. Dysregulated GRHL3 activity has been linked to developmental defects and epithelial pathologies, and altered expression patterns are reported in studies of squamous epithelia and carcinoma-associated transcriptional states. As a nuclear factor shaping epithelial gene expression, GRHL3 is frequently investigated in models of tissue morphogenesis, stress responses, and lineage commitment.
GRHL3 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the GRHL3 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the GRHL3 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 GRHL3 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 GRHL3 protein expression.
This CRISPR knockout system enables efficient generation of GRHL3-deficient cell models for investigation of GRHL3 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.