
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
TBL1XR1 CRISPR/Cas9 KO Plasmid (h) | sc-401998 | 20 µg | $397.00 |
TBL1XR1 (transducin β-like 1 X-linked receptor 1) encodes a WD40 repeat–containing coregulator that functions within NCoR/SMRT transcriptional repression complexes and participates in dynamic exchange between repression and activation at promoter and enhancer regions. It links chromatin-associated regulatory machinery to signal-dependent transcription programs, including pathways downstream of nuclear receptors and Wnt/β-catenin signaling, thereby influencing cell fate decisions, proliferation, and differentiation. Through its roles in transcriptional control and cofactor recruitment, TBL1XR1 has been implicated in oncogenic transcriptional states and in neurodevelopmental phenotypes reported in genetic studies. Perturbation of TBL1XR1 can therefore be used to interrogate chromatin-dependent gene regulation, transcriptional network stability, and pathway cross-talk in human cell models.
TBL1XR1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the TBL1XR1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the TBL1XR1 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 TBL1XR1 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 TBL1XR1 protein expression.
This CRISPR knockout system enables efficient generation of TBL1XR1-deficient cell models for investigation of TBL1XR1 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.