
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
PI 4-kinase II α CRISPR/Cas9 KO Plasmid (h) | sc-405423 | 20 µg | $397.00 |
PI4K2A encodes phosphatidylinositol 4-kinase II alpha (PI 4-kinase II alpha), a membrane-associated lipid kinase that generates phosphatidylinositol 4-phosphate (PI4P) to support phosphoinositide signaling and membrane identity. PI4P produced by PI4K2A contributes to Golgi and endosomal trafficking, clathrin-mediated sorting, and downstream phosphoinositide conversion that influences receptor transport and signaling dynamics. Through these roles in vesicle biogenesis and membrane remodeling, PI4K2A is relevant to studies of endomembrane organization, nutrient sensing, and stress responses. Altered phosphoinositide metabolism and trafficking programs linked to PI4K2A have been associated with mechanisms implicated in cancer biology, neurobiology, and host–pathogen interactions.
PI 4-kinase II α CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the PI4K2A gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the PI4K2A 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 PI4K2A 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 PI 4-kinase II α protein expression.
This CRISPR knockout system enables efficient generation of PI4K2A-deficient cell models for investigation of PI 4-kinase II α 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.