
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
TIEG1 CRISPR/Cas9 KO Plasmid (h) | sc-402480 | 20 µg | $397.00 |
KLF10 encodes TIEG1 (TGF-β inducible early growth response protein 1), a Krüppel-like zinc-finger transcription factor that integrates transforming growth factor-β (TGF-β)/SMAD signaling with context-dependent control of cell cycle progression, differentiation, and apoptosis. TIEG1 regulates transcriptional programs involved in extracellular matrix remodeling and lineage commitment, and it can modulate cross-talk with MAPK and hormonal signaling pathways in epithelial, bone, and immune cell contexts. Altered KLF10/TIEG1 activity has been associated with dysregulated fibrotic responses, aberrant osteoblast function and bone remodeling, and changes in tumor suppressive transcriptional networks, making it relevant for mechanistic studies of proliferation control and tissue homeostasis. Its role as an early response factor positions it as a useful node for dissecting stimulus-dependent gene regulation and downstream pathway wiring.
TIEG1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the KLF10 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the KLF10 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 KLF10 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 TIEG1 protein expression.
This CRISPR knockout system enables efficient generation of KLF10-deficient cell models for investigation of TIEG1 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.