
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
PILR-α CRISPR/Cas9 KO Plasmid (h) | sc-407310 | 20 µg | $397.00 |
PILRA (paired immunoglobulin-like type 2 receptor alpha) encodes an inhibitory cell-surface receptor enriched on myeloid populations, where it recognizes sialylated O-glycan ligands and transduces suppressive signaling through ITIM-dependent recruitment of phosphatases such as SHP-1/2. By dampening Fc receptor- and TLR-associated activation programs, PILR-α contributes to regulation of innate immune thresholds, cytokine output, and leukocyte effector functions. This checkpoint-like activity links PILR-α to pathways governing inflammatory homeostasis, antigen-presenting cell activation, and immune evasion mechanisms. Altered PILRA expression or ligand engagement has been implicated in neuroinflammation and infectious disease biology, making it relevant for studies of myeloid regulation in complex tissue microenvironments.
PILR-α CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the PILRA gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the PILRA 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 PILRA 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 PILR-α protein expression.
This CRISPR knockout system enables efficient generation of PILRA-deficient cell models for investigation of PILR-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.