
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
beta Actin CRISPR/Cas9 KO Plasmid (m) | sc-418965 | 20 µg | $397.00 |
Actb encodes mouse beta actin, a highly conserved cytoskeletal protein that polymerizes into microfilaments to support cell shape, polarity, and mechanical stability. Beta actin dynamics drive core processes including cytokinesis, vesicle trafficking, and cell migration through coordinated regulation of actin nucleation, branching, and turnover in pathways involving Rho family GTPases and actin-binding proteins. Beyond structural roles, actin remodeling influences transcriptional programs and signal transduction by modulating mechanotransduction and nuclear actin pools. Dysregulated actin organization is broadly implicated in experimental models of developmental defects, impaired wound repair, immune cell motility changes, and tumor cell invasion, making Actb a key reference locus in cell biology and disease mechanism studies.
beta Actin CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Actb gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Actb 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 Actb 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 beta Actin protein expression.
This CRISPR knockout system enables efficient generation of Actb-deficient cell models for investigation of beta Actin 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.