
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Neurogenin 3 CRISPR/Cas9 KO Plasmid (m) | sc-419234 | 20 µg | $397.00 |
Mouse Neurog3 encodes the basic helix–loop–helix transcription factor Neurogenin 3, a key determinant of endocrine lineage specification in the developing pancreas and gut. Neurogenin 3 integrates developmental signaling inputs, including Notch/Hes-mediated repression and pro-endocrine transcriptional cascades, to drive endocrine progenitor commitment and subsequent differentiation programs. Its activity coordinates gene regulatory networks controlling cell fate decisions, maturation, and hormone-producing cell identity, making Neurog3 a central node for studies of pancreatic development and endocrine cell biology. Dysregulated Neurog3 function is relevant to models of impaired endocrine differentiation and metabolic disease mechanisms involving pancreatic islet formation.
Neurogenin 3 CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Neurog3 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Neurog3 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 Neurog3 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 Neurogenin 3 protein expression.
This CRISPR knockout system enables efficient generation of Neurog3-deficient cell models for investigation of Neurogenin 3 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.