
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Integrin α4/ITGA4/CD49d CRISPR/Cas9 KO Plasmid (h) | sc-401336 | 20 µg | $397.00 |
ITGA4 encodes integrin α4 (CD49d), an adhesion receptor that heterodimerizes with β1 (VLA-4) or β7 to mediate cell–cell and cell–matrix interactions with ligands such as VCAM-1 and fibronectin. Through integrin outside-in signaling, ITGA4 influences cytoskeletal remodeling, focal adhesion dynamics, and downstream pathways including FAK/Src, PI3K–AKT, and MAPK that govern migration, survival, and activation states. Integrin α4 is a key regulator of leukocyte trafficking, immune synapse organization, and tissue homing, linking it to inflammatory circuitry and tumor–stroma interactions. Dysregulated ITGA4 activity or expression is frequently studied in contexts of chronic inflammation, immune cell infiltration, and hematologic malignancy cell adhesion within supportive niches.
Integrin α4/ITGA4/CD49d CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the ITGA4 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the ITGA4 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 ITGA4 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 α4/ITGA4/CD49d protein expression.
This CRISPR knockout system enables efficient generation of ITGA4-deficient cell models for investigation of Integrin α4/ITGA4/CD49d 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.