
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Carbonyl reductase 3 CRISPR/Cas9 KO Plasmid (h) | sc-406552 | 20 µg | $397.00 |
CBR3 encodes carbonyl reductase 3, a cytosolic NADPH-dependent oxidoreductase that catalyzes the reduction of reactive carbonyl compounds, including aldehydes and ketones generated during xenobiotic metabolism and oxidative stress. By modulating cellular redox balance and carbonyl detoxification, CBR3 contributes to phase I/II metabolic processes and helps limit accumulation of electrophilic intermediates that can damage proteins, lipids, and DNA. Variation in CBR3 activity has been studied in the context of differential handling of endogenous lipid peroxidation products and diverse small-molecule substrates, linking this enzyme to pathways relevant to stress responses and metabolic adaptation. Altered carbonyl reductase activity is frequently investigated in cancer biology, pharmacology, and toxicology models where redox state and metabolite processing influence cell survival and phenotype.
Carbonyl reductase 3 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CBR3 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CBR3 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 CBR3 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 Carbonyl reductase 3 protein expression.
This CRISPR knockout system enables efficient generation of CBR3-deficient cell models for investigation of Carbonyl reductase 3 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.