
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Mitofilin CRISPR/Cas9 KO Plasmid (m) | sc-429376 | 20 µg | $397.00 |
Mouse Immt encodes mitofilin, a core component of the MICOS (mitochondrial contact site and cristae organizing system) complex that maintains inner mitochondrial membrane architecture and crista junction formation. Mitofilin supports mitochondrial ultrastructure, coordinates contacts between the inner and outer membranes, and influences protein import and respiratory chain organization important for oxidative phosphorylation. Disruption of IMMT perturbs cristae morphology, mitochondrial dynamics, and bioenergetic homeostasis, processes that are widely implicated in neurodegeneration, cardiomyopathy, metabolic dysfunction, and cancer cell adaptation. As a nexus of mitochondrial structure–function coupling, Immt is frequently studied in pathways governing apoptosis sensitivity, mitophagy, and cellular stress responses.
Mitofilin CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Immt gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Immt 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 Immt 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 Mitofilin protein expression.
This CRISPR knockout system enables efficient generation of Immt-deficient cell models for investigation of Mitofilin 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.