
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Glucose Transporter Glut2 CRISPR/Cas9 KO Plasmid (h) | sc-400347 | 20 µg | $397.00 |
SLC2A2 encodes glucose transporter 2 (GLUT2), a facilitative hexose transporter that mediates bidirectional glucose flux across the plasma membrane in a concentration-dependent manner. In human tissues, GLUT2 contributes to nutrient sensing and metabolic homeostasis by supporting glucose uptake and release and influencing downstream pathways linked to glycolysis, gluconeogenesis, and insulin secretion dynamics. Altered SLC2A2 expression or function has been associated with dysregulated glucose handling and metabolic phenotypes, making it relevant for studies of diabetes biology, hepatic glucose output, and pancreatic islet function. Because GLUT2 can also transport other hexoses, perturbation of SLC2A2 impacts broader carbohydrate utilization and cellular energy balance.
Glucose Transporter Glut2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the SLC2A2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the SLC2A2 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 SLC2A2 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 Glut2 protein expression.
This CRISPR knockout system enables efficient generation of SLC2A2-deficient cell models for investigation of Glucose Transporter Glut2 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.