
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
CUG-BP2 CRISPR/Cas9 KO Plasmid (h) | sc-403267 | 20 µg | $397.00 |
CELF2 (CUG-BP2) is an RNA-binding protein of the CELF family that coordinates post-transcriptional gene regulation by controlling alternative splicing, mRNA stability, and translation across diverse transcripts. It participates in coupling RNA processing to signaling inputs during cell differentiation and stress responses, influencing networks involved in cytoskeletal organization, cell-cycle control, and apoptosis. CELF2-dependent RNA programs contribute to tissue-specific transcript isoform selection and are frequently studied in the context of immune cell activation and developmental gene regulation. Dysregulated CELF2 activity has been associated with altered splicing landscapes observed in neuromuscular and cancer-related models, motivating mechanistic studies of its RNA targets and regulatory partners.
CUG-BP2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CELF2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CELF2 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 CELF2 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 CUG-BP2 protein expression.
This CRISPR knockout system enables efficient generation of CELF2-deficient cell models for investigation of CUG-BP2 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.