
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Glucose Transporter Glut10 CRISPR/Cas9 KO Plasmid (m) | sc-431260 | 20 µg | $397.00 |
Slc2a10 encodes glucose transporter GLUT10, a facilitative hexose transporter that contributes to cellular carbohydrate handling and redox homeostasis in mouse tissues. GLUT10 has been linked to intracellular transport of glucose or dehydroascorbate, connecting sugar flux with antioxidant pathways that influence mitochondrial function and extracellular matrix maintenance. Through these roles, Slc2a10 is relevant to studies of metabolic adaptation, oxidative stress responses, and vascular connective tissue biology. Genetic disruption of Slc2a10 is used to probe mechanisms underlying arterial tortuosity syndrome–like phenotypes, altered collagen/elastin organization, and stress-sensitive metabolic remodeling in experimental models.
Glucose Transporter Glut10 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Slc2a10 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Slc2a10 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 Slc2a10 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 Glucose Transporter Glut10 protein expression.
This CRISPR knockout system enables efficient generation of Slc2a10-deficient cell models for investigation of Glucose Transporter Glut10 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.