
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
eIF3η CRISPR/Cas9 KO Plasmid (h) | sc-400817 | 20 µg | $397.00 |
EIF3B encodes a core subunit of the eukaryotic translation initiation factor 3 (eIF3) complex, eIF3η, which coordinates 40S ribosomal subunit recruitment and assembly of the preinitiation complex during cap-dependent translation. Through interactions with additional initiation factors and mRNA, eIF3η supports start-codon selection and controls translation efficiency of transcripts linked to growth, metabolism, and stress adaptation. EIF3B function intersects with pathways regulating proteostasis and cell-cycle progression, and dysregulated translation initiation is frequently associated with oncogenic signaling and altered cellular fitness. As a central node in translational control, EIF3B is commonly studied in contexts of proliferation, stress responses, and transformation-associated changes in protein synthesis programs.
eIF3η CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the EIF3B gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the EIF3B 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 EIF3B 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 eIF3η protein expression.
This CRISPR knockout system enables efficient generation of EIF3B-deficient cell models for investigation of eIF3η 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.