
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Rho T2 CRISPR/Cas9 KO Plasmid (h) | sc-406496 | 20 µg | $397.00 |
RHOT2 encodes Rho T2 (also known as Miro2), an atypical Rho-family GTPase anchored in the outer mitochondrial membrane that helps coordinate mitochondrial trafficking, positioning, and quality control. Through interactions with adaptor proteins linking mitochondria to microtubule motors, RHOT2 contributes to cytoskeletal-dependent transport and supports mitochondrial distribution required for energy-demanding cellular regions. Rho T2 is also implicated in calcium-sensitive regulation of mitochondrial dynamics and turnover, intersecting with pathways governing mitochondrial homeostasis and stress responses. Dysregulated RHOT2 function has been studied in the context of altered mitochondrial dynamics and bioenergetics, processes frequently associated with neurodegeneration and cancer-related metabolic reprogramming.
Rho T2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the RHOT2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the RHOT2 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 RHOT2 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 Rho T2 protein expression.
This CRISPR knockout system enables efficient generation of RHOT2-deficient cell models for investigation of Rho T2 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.