Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
ZO-1 Double Nickase Plasmid (m): sc-423407-NIC
- Target species: mouse
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- ZO-1 Double Nickase Plasmid (m) consists of a pair of plasmids each encoding a D10A mutated Cas9 nuclease and a target-specific 20 nt guide RNA (gRNA) designed to knockout gene expression with greater specificity than its CRISPR/Cas9 KO counterpart
- Paired gRNA sequences are offset by approximately 20 bp to allow for specific Cas9-mediated double nicking of the genomic DNA, which mimics a DSB
- One plasmid in the pair contains a puromycin-resistance gene for selection; the other plasmid in the pair contains a GFP marker to visually confirm transfection
- ZO-1 Double Nickase Plasmid (m) and ZO-1 Double Nickase Plasmid (m2) encode distinct paired gRNA designs targeting Tjp1. One or both designs may be available
- Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: ZO-1 Antibody (R40.76): sc-33725
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
ZO-1 Double Nickase Plasmid (m) | sc-423407-NIC | 20 µg | $410.00 |
Mouse Tjp1 encodes the tight junction scaffolding protein ZO-1 (TJP1), a membrane-associated guanylate kinase family member that links claudins and occludin to the cortical actin cytoskeleton to organize apical–basal polarity and paracellular barrier function. ZO-1 participates in tight junction assembly and maintenance, integrating signals from Rho GTPase–regulated cytoskeletal dynamics and junctional mechanotransduction, and it can influence contact-dependent signaling pathways that coordinate epithelial organization. Altered ZO-1 localization or expression is commonly used as a readout of tight junction integrity in models of epithelial and endothelial barrier dysfunction. In mouse systems, Tjp1 perturbation supports mechanistic studies of permeability, inflammation-associated barrier remodeling, and developmental processes requiring precise junctional architecture.
ZO-1 Double Nickase Plasmid (m) consists of a matched pair of plasmids engineered for high-specificity editing of the Tjp1 locus in mouse cell lines. Each plasmid expresses a Cas9 D10A nickase and a distinct sgRNA targeting opposite DNA strands within Tjp1. When directed to adjacent sites on opposite DNA strands, the two nickases generate offset single-strand nicks that together produce a staggered double-strand break, requiring coordinated on-target activity from both guides. The resulting DNA break is resolved by endogenous cellular repair pathways, most commonly through non-homologous end joining (NHEJ), leading to insertions or deletions that disrupt Tjp1 function. By requiring dual sgRNA engagement at the target locus, the double nicking approach enhances editing specificity and provides a complementary CRISPR strategy for applications where additional control over targeting precision is desired.
To support efficient identification of edited cells, one plasmid encodes GFP for fluorescent visualization of transfected populations, while the companion plasmid carries a puromycin resistance gene for antibiotic selection. Together, these features support efficient enrichment of co-transfected populations and simplify the validation of Tjp1-disrupted clones.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.