
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
CPSF2 CRISPR/Cas9 KO Plasmid (h) | sc-407012 | 20 µg | $397.00 |
CPSF2 (cleavage and polyadenylation specificity factor subunit 2) is a core component of the mammalian 3′ end mRNA processing machinery that contributes to recognition of polyadenylation signals and assembly of the cleavage and polyadenylation complex. Through its role in pre-mRNA cleavage and poly(A) tail addition, CPSF2 influences transcript maturation, mRNA stability, and translation efficiency, thereby shaping global gene-expression programs. CPSF2-dependent 3′ end processing also interfaces with transcription termination and alternative polyadenylation, processes that remodel the transcriptome during proliferation and differentiation. Dysregulation of 3′ end formation and polyadenylation-site selection is frequently observed in disease-associated expression states, making CPSF2 a useful node for investigating RNA-processing phenotypes and their downstream cellular effects.
CPSF2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CPSF2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CPSF2 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 CPSF2 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 CPSF2 protein expression.
This CRISPR knockout system enables efficient generation of CPSF2-deficient cell models for investigation of CPSF2 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.