
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
IL-1RAcP CRISPR/Cas9 KO Plasmid (m) | sc-421101 | 20 µg | $397.00 |
Il1rap encodes IL-1RAcP, an essential co-receptor that complexes with IL-1 receptor family members to propagate signals initiated by IL-1α/IL-1β and related ligands. Upon receptor engagement, IL-1RAcP supports assembly of MyD88-dependent signaling complexes that activate IRAK–TRAF6 cascades, leading to NF-κB and MAPK pathway activation and downstream transcriptional programs controlling inflammation, innate immune responses, and stromal–immune communication. In mouse models, altered IL-1R/IL-1RAcP signaling is frequently used to study mechanisms driving chronic inflammatory states, tissue injury responses, and cytokine-amplified remodeling in diverse organ systems. Because IL-1RAcP integrates multiple IL-1 family inputs, it is relevant for dissecting pathway crosstalk that shapes leukocyte recruitment, barrier function, and inflammatory gene expression.
IL-1RAcP CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Il1rap gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Il1rap 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 Il1rap 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 IL-1RAcP protein expression.
This CRISPR knockout system enables efficient generation of Il1rap-deficient cell models for investigation of IL-1RAcP 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.