GATA-6 CRISPR/Cas9 KO Plasmid (m): sc-420498
- Target species: mouse
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- GATA-6 CRISPR/Cas9 Knockout (KO) Plasmid (m) 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 GATA-6 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
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
GATA-6 CRISPR/Cas9 KO Plasmid (m) | sc-420498 | 20 µg | $397.00 |
Overview
Mouse Gata6 encodes the zinc finger transcription factor GATA-6, a key regulator of endodermal lineage specification and epithelial differentiation during embryogenesis and adult tissue homeostasis. GATA-6 modulates gene programs controlling cell fate decisions, morphogenesis, and organ development, including processes in the respiratory and gastrointestinal systems. It integrates with developmental transcriptional networks and signaling pathways such as WNT, BMP/TGF-β, and FGF to coordinate context-dependent transcriptional outputs. Dysregulated GATA-6 activity has been linked to developmental abnormalities and altered differentiation states that are relevant to modeling congenital defects and mechanisms of disease-associated tissue remodeling.
GATA-6 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Gata6 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Gata6 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 Gata6 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 GATA-6 protein expression.
This CRISPR knockout system enables efficient generation of Gata6-deficient cell models for investigation of GATA-6 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
Key Features
- sgRNAs targeting Gata6 exon(s) critical for GATA-6 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 Gata6 genomic sites to improve knockout efficiency
- Compatible with delivery by transfection
Design Variants
CRISPRs +/- HDRs
- gRNAs encoded by GATA-6 CRISPR/Cas9 KO Plasmid (m) and GATA-6 CRISPR/Cas9 KO Plasmid (m2) target distinct sites within the Gata6 locus. One or both targeting designs may be available. See Related Products for availability.
- HDR donor constructs encoded by GATA-6 HDR Plasmid (m) and GATA-6 HDR Plasmid (m2) contain a puromycin resistance cassette and an RFP reporter flanked by Gata6 homology arms to support homology-directed repair at defined Gata6 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.