Doublecortin CRISPR/Cas9 KO Plasmid (r): sc-437358
- Target species: rat
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- Doublecortin CRISPR/Cas9 Knockout (KO) Plasmid (r) is a pool of plasmids, each encoding Cas9 nuclease and a target-specific 20 nt guide RNA (gRNA) designed for maximum knockout efficiency using sequences derived from the GeCKO v2 library
- gRNA sequences direct Cas9 to induce site-specific double-strand breaks (DSBs) in the Doublecortin genomic locus, resulting in gene knockout through non-homologous end joining (NHEJ)
- The puromycin resistance and RFP genes are flanked by LoxP sites, enabling removal of selection markers via Cre recombinase (Cre Vector: sc-418923) after establishing stable knockout cell lines
- Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: Doublecortin/DCX Antibody (E-6): sc-271390
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Doublecortin CRISPR/Cas9 KO Plasmid (r) | sc-437358 | 20 µg | $397.00 |
Overview
Doublecortin (DCX) is a neuronal microtubule-associated protein that binds and stabilizes microtubules to regulate cytoskeletal dynamics during neurogenesis. It is highly expressed in migrating neuroblasts and immature neurons, where it supports neurite outgrowth, neuronal polarization, and cortical layering through control of microtubule polymerization and intracellular transport. DCX intersects with pathways governing actin–microtubule coordination, centrosome positioning, and axon guidance, linking cytoskeletal remodeling to developmental patterning. Disruption of DCX function is associated with neurodevelopmental abnormalities and altered neuronal connectivity, making it a widely used marker and mechanistic node in studies of neuronal migration and brain development.
Doublecortin CRISPR/Cas9 KO Plasmid (r) is a pool of plasmids designed for targeted disruption of the gene in rat cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the 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 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 Doublecortin protein expression.
This CRISPR knockout system enables efficient generation of -deficient cell models for investigation of Doublecortin signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
Key Features
- sgRNAs targeting exon(s) critical for Doublecortin function
- Co-expression of SpCas9 and sgRNA from a single plasmid for simplified delivery
- GFP reporter for identification of transfected cells
- Pool of plasmids targeting multiple genomic sites to improve knockout efficiency
- Compatible with delivery by transfection
Design Variants
CRISPRs +/- HDRs
- gRNAs encoded by Doublecortin CRISPR/Cas9 KO Plasmid (r) and Doublecortin CRISPR/Cas9 KO Plasmid (r2) target distinct sites within the locus. One or both targeting designs may be available. See Related Products for availability.
- HDR donor constructs encoded by Doublecortin HDR Plasmid (r) and Doublecortin HDR Plasmid (r2) contain a puromycin resistance cassette and an RFP reporter flanked by homology arms to support homology-directed repair at defined target sites corresponding to the CRISPR/Cas9 KO designs. HDR donor availability may vary. See Related Products for availability.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.