
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Integrin β4/ITGB4/CD104 CRISPR/Cas9 KO Plasmid (h2) | sc-400573-KO-2 | 20 µg | $397.00 | |||
Integrin β4/ITGB4/CD104 HDR Plasmid (h2) | sc-400573-HDR-2 | 20 µg | $445.00 |
ITGB4 encodes integrin β4 (CD104), a transmembrane adhesion receptor that pairs primarily with integrin α6 to form α6β4, a key component of hemidesmosomes that anchors epithelial cells to the basement membrane via laminins. Through its unusually long cytoplasmic tail, integrin β4 coordinates cytoskeletal organization and bidirectional signaling that influences cell polarity, migration, and survival, interfacing with pathways such as PI3K–AKT, MAPK, and focal adhesion/hemidesmosome remodeling. ITGB4 function is central to epithelial barrier integrity and tissue architecture, and dysregulation of α6β4-mediated adhesion and signaling has been associated with altered invasive behavior and tumor progression in multiple epithelial contexts. These properties make ITGB4 a frequent target for mechanistic studies of cell–matrix interactions, junctional stability, and signaling crosstalk in normal and disease-relevant models.
Integrin β4/ITGB4/CD104 CRISPR/Cas9 KO Plasmid (h2) is a pool of plasmids designed for targeted disruption of the ITGB4 gene in human cell lines. Each plasmid in the pool co-expresses a unique sgRNA, targeting a distinct site within the ITGB4 locus, alongside the Streptococcus pyogenes Cas9 nuclease, and encodes GFP to enable fluorescent identification and enrichment of successfully transfected cells. This multi-guide strategy increases the likelihood of inducing frameshifts or deletions that produce a functional knockout, offering a more robust alternative to single-guide approaches. DSBs induced at multiple sites are resolved through non-homologous end joining (NHEJ) or, when used with the included HDR donor template, homology-directed repair (HDR) at a defined target site within the locus.
When used in conjunction with the RFP-expressing HDR donor, GFP and RFP fluorescence can be used together to distinguish transfected from edited cell populations, streamlining flow cytometry-based sorting and clone selection workflows.
For applications requiring confirmed, selectable knockout clones, Integrin β4/ITGB4/CD104 HDR Plasmid (h2) includes an HDR donor construct containing a puromycin resistance cassette (PuroR) and a red fluorescent protein (RFP) reporter, flanked by homology arms specific to a defined ITGB4 target site.
When co-transfected with Integrin β4/ITGB4/CD104 CRISPR/Cas9 KO Plasmid (h2):
The HDR donor construct features loxP sites flanking the PuroR-RFP selection cassette to allow clean marker removal following clone confirmation. Transient expression of Cre recombinase via the included Cre Vector: sc-418923 excises the cassette, leaving a minimal residual loxP site within the ITGB4 locus and eliminating potential confounding effects on downstream assays.
This two-step approach:
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.