
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Importin-7 CRISPR/Cas9 KO Plasmid (h) | sc-403562 | 20 µg | $397.00 |
IPO7 encodes Importin-7, a karyopherin-β family nuclear transport receptor that mediates RanGTP-dependent import of diverse cargo proteins and ribonucleoprotein complexes through the nuclear pore. Importin-7 supports nuclear localization of regulatory factors involved in transcriptional control, ribosome biogenesis, and innate immune signaling, linking nucleocytoplasmic trafficking to cell-cycle progression and stress responses. Through its role in controlling nuclear availability of signaling and chromatin-associated proteins, IPO7 can influence pathways that govern proliferation and genome maintenance. Dysregulated nuclear transport has been associated with oncogenic programs and altered host–pathogen interactions, making IPO7 a useful node for mechanistic studies of transport-dependent phenotypes.
Importin-7 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the IPO7 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the IPO7 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 IPO7 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 Importin-7 protein expression.
This CRISPR knockout system enables efficient generation of IPO7-deficient cell models for investigation of Importin-7 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.