
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
TMEM70 CRISPR/Cas9 KO Plasmid (h) | sc-412399 | 20 µg | $397.00 |
TMEM70 encodes a mitochondrial inner membrane protein required for proper assembly and stabilization of oxidative phosphorylation complex V (ATP synthase), supporting efficient ATP production and mitochondrial energy homeostasis. Loss or dysfunction of TMEM70 perturbs proton-coupled ATP synthesis, often leading to altered mitochondrial membrane potential, disrupted respiratory chain function, and compensatory metabolic remodeling. TMEM70 is therefore a useful node for studying mitochondrial biogenesis, bioenergetics, and mitonuclear coordination in human cells. Pathogenic TMEM70 variants have been linked to autosomal recessive mitochondrial disease, including complex V deficiency with encephalocardiomyopathy and metabolic decompensation phenotypes, motivating mechanistic studies in relevant cell models.
TMEM70 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the TMEM70 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the TMEM70 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 TMEM70 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 TMEM70 protein expression.
This CRISPR knockout system enables efficient generation of TMEM70-deficient cell models for investigation of TMEM70 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.