
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
I2PP2A CRISPR/Cas9 KO Plasmid (h) | sc-400881 | 20 µg | $397.00 |
SET (also known as I2PP2A) encodes a multifunctional nuclear and cytoplasmic protein that inhibits protein phosphatase 2A (PP2A), thereby influencing phosphorylation-dependent control of cell cycle progression, apoptosis, and transcriptional programs. I2PP2A participates in chromatin regulation through interactions with histones and chromatin-associated complexes, linking SET to DNA damage responses, replication stress, and epigenetic modulation of gene expression. By restraining PP2A activity, SET can impact key signaling axes such as MAPK/ERK and PI3K/AKT that depend on balanced phosphorylation turnover. Dysregulated SET expression or activity has been associated with oncogenic signaling states and neuroinflammatory or neurodegenerative processes, making it a useful target for mechanistic studies of phosphatase regulation and chromatin-associated pathways.
I2PP2A CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the SET gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the SET 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 SET 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 I2PP2A protein expression.
This CRISPR knockout system enables efficient generation of SET-deficient cell models for investigation of I2PP2A 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.