
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
BTBD4 CRISPR/Cas9 KO Plasmid (m) | sc-428253 | 20 µg | $397.00 |
Zbtb46 encodes the BTBD4 protein, a BTB/POZ domain–containing factor implicated in transcriptional regulation programs that shape cell identity and differentiation states in mouse tissues. In immune biology, Zbtb46 expression is widely used as a marker of classical dendritic cell lineage, and its regulatory activity is studied in the context of antigen presentation, inflammatory signaling, and homeostatic immune surveillance. Altered Zbtb46-associated gene networks have been examined in models of tumor-associated immunity and inflammatory disease, where shifts in dendritic cell function can influence cytokine profiles and T cell priming. As a result, Zbtb46/BTBD4 perturbation is a useful approach for dissecting transcriptional circuits connecting differentiation, innate immune pathways, and microenvironmental responses.
BTBD4 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Zbtb46 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Zbtb46 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 Zbtb46 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 BTBD4 protein expression.
This CRISPR knockout system enables efficient generation of Zbtb46-deficient cell models for investigation of BTBD4 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.