
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
GMF-β CRISPR/Cas9 KO Plasmid (m) | sc-425657 | 20 µg | $397.00 |
Glia maturation factor beta (GMF-β), encoded by the mouse Gmfb gene, is a conserved cytosolic regulator of actin cytoskeleton remodeling that influences cell shape changes and motility in neural and immune-related contexts. GMF-β interacts with the Arp2/3 complex to modulate actin branch dynamics, linking it to pathways governing neurite outgrowth, synaptic remodeling, and glial cell responses to environmental cues. In the central nervous system, GMF-β has been studied in relation to neuroinflammatory signaling and stress-associated cellular activation programs, where altered cytoskeletal regulation can impact tissue homeostasis. Dysregulated GMF-β–associated processes have relevance to experimental models of neurodegeneration and inflammatory injury through effects on cell migration, reactive gliosis, and cytoskeletal-dependent signaling.
GMF-β CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Gmfb gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Gmfb 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 Gmfb 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 GMF-β protein expression.
This CRISPR knockout system enables efficient generation of Gmfb-deficient cell models for investigation of GMF-β 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.