
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Oma1 CRISPR/Cas9 KO Plasmid (h) | sc-402953 | 20 µg | $397.00 |
OMA1 encodes a stress-activated metalloprotease embedded in the inner mitochondrial membrane that contributes to mitochondrial quality control by proteolytically processing substrates such as OPA1 to remodel cristae architecture and regulate mitochondrial fusion–fission dynamics. Oma1 activity is induced by mitochondrial depolarization and proteotoxic stress, integrating signals that influence oxidative phosphorylation efficiency, reactive oxygen species handling, and mitophagy-linked surveillance. Through its impact on organelle morphology and bioenergetics, OMA1 is studied in pathways governing apoptosis susceptibility and metabolic adaptation. Dysregulated OMA1–OPA1 axis function has been associated with mitochondrial dysfunction phenotypes relevant to neurodegeneration, cardiometabolic stress, and other disorders where impaired mitochondrial dynamics are implicated.
Oma1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the OMA1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the OMA1 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 OMA1 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 Oma1 protein expression.
This CRISPR knockout system enables efficient generation of OMA1-deficient cell models for investigation of Oma1 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.