
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
GBP1 CRISPR/Cas9 KO Plasmid (h) | sc-401778 | 20 µg | $397.00 |
Guanylate binding protein 1 (GBP1) is a large interferon-inducible dynamin-like GTPase that acts as an effector of innate immunity. It is robustly upregulated downstream of JAK/STAT signaling in response to type I and type II interferons and participates in cell-autonomous defense by targeting pathogen-containing compartments and modulating antimicrobial and inflammatory programs. GBP1 has been linked to processes including inflammasome-related responses, intracellular trafficking, and cytoskeletal remodeling, with context-dependent roles in epithelial barrier biology and immune cell activation. Altered GBP1 expression is frequently observed in chronic inflammatory states, infectious disease models, and tumor-associated immune microenvironments, making it a useful node for studying interferon-stimulated gene (ISG) networks.
GBP1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the GBP1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the GBP1 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 GBP1 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 GBP1 protein expression.
This CRISPR knockout system enables efficient generation of GBP1-deficient cell models for investigation of GBP1 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.