NCoA-5 Double Nickase Plasmid (m): sc-432820-NIC
- Target species: mouse
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- NCoA-5 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
- NCoA-5 Double Nickase Plasmid (m) and NCoA-5 Double Nickase Plasmid (m2) encode distinct paired gRNA designs targeting Ncoa5. One or both designs may be available
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
NCoA-5 Double Nickase Plasmid (m) | sc-432820-NIC | 20 µg | $410.00 |
Ncoa5 encodes nuclear receptor coactivator 5 (NCoA-5), a transcriptional coregulator that modulates gene expression by interacting with ligand-activated nuclear receptors and other transcription factors. In mouse cells, NCoA-5 contributes to chromatin-dependent regulation of metabolic and inflammatory transcriptional programs, linking nuclear receptor signaling to cell-state decisions. Altered NCoA-5 activity has been associated with dysregulated insulin and lipid homeostasis and pro-inflammatory gene expression in experimental models, supporting its relevance to studies of metabolic syndrome–like phenotypes. These properties make Ncoa5 a useful target for dissecting transcriptional networks that integrate hormone signaling, epigenetic regulation, and immune-metabolic crosstalk.
NCoA-5 Double Nickase Plasmid (m) consists of a matched pair of plasmids engineered for high-specificity editing of the Ncoa5 locus in mouse cell lines. Each plasmid expresses a Cas9 D10A nickase and a distinct sgRNA targeting opposite DNA strands within Ncoa5. 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 Ncoa5 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 Ncoa5-disrupted clones.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.