
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
palladin CRISPR/Cas9 KO Plasmid (m2) | sc-428317-KO-2 | 20 µg | $397.00 |
Mouse Palld encodes palladin, an actin-associated scaffolding protein that coordinates cytoskeletal organization by binding actin regulators and crosslinking components at stress fibers, focal adhesions, and other adhesion complexes. Palladin supports cell shape control, adhesion maturation, and directed migration, integrating signaling from Rho family GTPases and pathways governing actomyosin contractility and extracellular matrix interactions. Altered palladin expression or localization has been linked to abnormal tissue remodeling and invasive phenotypes in cancer-relevant contexts, making Palld a useful node for studying cytoskeletal dysregulation. In the mouse system, Palld perturbation is commonly used to dissect mechanisms of motility, mechanotransduction, and adhesion-dependent signaling in development and disease models.
palladin CRISPR/Cas9 KO Plasmid (m2) is a pool of plasmids designed for targeted disruption of the Palld gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Palld 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 Palld 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 palladin protein expression.
This CRISPR knockout system enables efficient generation of Palld-deficient cell models for investigation of palladin 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.