KV1.5 Double Nickase Plasmid (h): sc-404341-NIC
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- KV1.5 Double Nickase Plasmid (h) 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
- KV1.5 Double Nickase Plasmid (h) and KV1.5 Double Nickase Plasmid (h2) encode distinct paired gRNA designs targeting KCNA5. One or both designs may be available
- Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: KV1.5 Antibody (A-3): sc-377110
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
KV1.5 Double Nickase Plasmid (h) | sc-404341-NIC | 20 µg | $410.00 | |||
KV1.5 Double Nickase Plasmid (h2) | sc-404341-NIC-2 | 20 µg | $410.00 |
KCNA5 encodes the human voltage-gated potassium channel subunit KV1.5, a delayed rectifier conductance that shapes membrane repolarization and controls cellular excitability. In cardiac and excitable tissues, KV1.5 contributes to action potential duration and integrates with ion homeostasis networks that regulate calcium handling and electrical signaling. The channel also influences proliferation and migration programs in non-excitable cells through membrane potential–dependent control of signaling and cell-cycle checkpoints. Altered KCNA5 expression or channel function has been associated with atrial electrophysiology phenotypes and broader channelopathy-relevant mechanisms, supporting its use in studies of electrical remodeling and signal transduction.
KV1.5 Double Nickase Plasmid (h) consists of a matched pair of plasmids engineered for high-specificity editing of the KCNA5 locus in human cell lines. Each plasmid expresses a Cas9 D10A nickase and a distinct sgRNA targeting opposite DNA strands within KCNA5. 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 KCNA5 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 KCNA5-disrupted clones.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.