
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Grim19 CRISPR/Cas9 KO Plasmid (h) | sc-403264 | 20 µg | $397.00 |
NDUFA13 (GRIM19) encodes a conserved accessory subunit of mitochondrial complex I that supports oxidative phosphorylation and proper electron transfer within the respiratory chain. Grim19 contributes to maintenance of mitochondrial membrane potential and cellular bioenergetics, linking mitochondrial metabolism to redox homeostasis and apoptotic susceptibility. Beyond its role in complex I assembly and function, GRIM19 has been reported to interface with signal transduction programs such as STAT3-dependent transcription, providing a connection between mitochondrial status and nuclear gene regulation. Dysregulation of NDUFA13/Grim19 is associated with mitochondrial dysfunction phenotypes and has been studied in contexts where altered respiration and stress signaling contribute to disease-relevant cellular states.
Grim19 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the NDUFA13 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the NDUFA13 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 NDUFA13 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 Grim19 protein expression.
This CRISPR knockout system enables efficient generation of NDUFA13-deficient cell models for investigation of Grim19 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.