
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
CYP2J2 CRISPR/Cas9 KO Plasmid (h) | sc-402955 | 20 µg | $397.00 |
CYP2J2 encodes a microsomal cytochrome P450 monooxygenase that catalyzes NADPH-dependent oxidation of endogenous lipids and xenobiotics, with notable epoxygenase activity toward arachidonic acid to generate epoxyeicosatrienoic acids (EETs). These metabolites contribute to regulation of vascular tone, inflammatory signaling, cellular proliferation, and oxidative stress responses, linking CYP2J2 activity to eicosanoid and lipid mediator pathways. CYP2J2 expression in cardiovascular and extrahepatic tissues supports roles in endothelial function and metabolic homeostasis, and altered expression or activity has been associated with cardiometabolic and inflammatory phenotypes. In cancer biology, CYP2J2-dependent lipid signaling has been investigated in relation to tumor cell survival, migration, and microenvironmental crosstalk, making it a useful target for mechanistic studies.
CYP2J2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CYP2J2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CYP2J2 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 CYP2J2 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 CYP2J2 protein expression.
This CRISPR knockout system enables efficient generation of CYP2J2-deficient cell models for investigation of CYP2J2 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.