
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Integrin αIIb/ITGA2B/CD41 CRISPR/Cas9 KO Plasmid (m) | sc-421160 | 20 µg | $397.00 |
Itga2b encodes integrin αIIb (CD41), which pairs with integrin β3 (CD61) to form the platelet fibrinogen receptor αIIbβ3, a central mediator of platelet adhesion and aggregation. Upon activation, αIIbβ3 undergoes inside-out and outside-in signaling that links extracellular matrix ligands such as fibrinogen and von Willebrand factor to cytoskeletal remodeling, focal adhesion dynamics, and Src/FAK-dependent signaling pathways. In mice, Itga2b expression marks megakaryocyte lineage commitment and supports platelet production and hemostatic responses. Dysregulated integrin signaling and altered platelet activation are broadly relevant to studies of thrombocytopenia, bleeding phenotypes, inflammation-associated thrombosis, and platelet–immune crosstalk in vascular disease models.
Integrin αIIb/ITGA2B/CD41 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Itga2b gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Itga2b 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 Itga2b 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 Integrin αIIb/ITGA2B/CD41 protein expression.
This CRISPR knockout system enables efficient generation of Itga2b-deficient cell models for investigation of Integrin αIIb/ITGA2B/CD41 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.