
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
PABP CRISPR/Cas9 KO Plasmid (m) | sc-422100 | 20 µg | $397.00 |
Mouse Pabpc1 encodes poly(A)-binding protein (PABP), a central regulator of cytoplasmic mRNA fate that binds poly(A) tails and coordinates translation initiation, mRNA stabilization, and deadenylation-dependent turnover. Through interactions with eIF4G and other RNA-binding proteins, PABP helps couple poly(A) tail length to ribosome recruitment and supports efficient protein synthesis during growth, differentiation, and stress responses. PABP also contributes to post-transcriptional control programs implicated in cell-cycle progression, apoptosis, and innate antiviral responses, making Pabpc1 a relevant node in studies of dysregulated gene expression. Perturbation of PABP-dependent mRNA regulatory networks is commonly examined in the context of oncogenic translation programs and neurodevelopmental or neurodegenerative phenotypes driven by altered RNA metabolism.
PABP CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Pabpc1 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Pabpc1 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 Pabpc1 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 PABP protein expression.
This CRISPR knockout system enables efficient generation of Pabpc1-deficient cell models for investigation of PABP 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.