
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
WTAP CRISPR/Cas9 KO Plasmid (m) | sc-425635 | 20 µg | $397.00 |
Wtap encodes WTAP (Wilms tumor 1–associating protein), a core regulatory component of the mRNA N6-methyladenosine (m6A) writer complex that supports METTL3/METTL14 catalytic activity and coordinates nuclear localization of methylation machinery. Through m6A-dependent control of pre-mRNA processing, alternative splicing, transcript stability, and translation, WTAP influences cell-cycle progression, lineage specification, and stress-responsive gene expression programs. WTAP activity interfaces with RNA metabolism pathways in nuclear speckles and links epitranscriptomic regulation to developmental signaling and differentiation networks. Dysregulated WTAP-associated m6A deposition has been implicated in altered proliferation and differentiation states relevant to cancer biology and hematopoietic and developmental phenotypes in model systems.
WTAP CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Wtap gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Wtap 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 Wtap 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 WTAP protein expression.
This CRISPR knockout system enables efficient generation of Wtap-deficient cell models for investigation of WTAP 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.