
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
TFIIIB′′ CRISPR/Cas9 KO Plasmid (m) | sc-436781 | 20 µg | $397.00 |
Bdp1 encodes the mouse TFIIIB″ subunit, a core component of the RNA polymerase III transcription machinery that cooperates with TBP and BRF proteins to assemble TFIIIB at Pol III promoters. TFIIIB″ supports initiation and reinitiation of Pol III–dependent transcription of tRNAs, 5S rRNA, and other small noncoding RNAs, linking Bdp1 activity to translational capacity, proteostasis, and cellular growth control. Because Pol III output is tightly coupled to nutrient sensing and stress responses, perturbation of Bdp1 can influence cell-cycle progression and metabolic adaptation. Dysregulated Pol III transcription and altered TFIIIB function are frequently studied in contexts of proliferative disorders and genome stability pathways, making Bdp1 a useful target for mechanistic studies in mammalian cells.
TFIIIB″ CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Bdp1 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Bdp1 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 Bdp1 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 TFIIIB″ protein expression.
This CRISPR knockout system enables efficient generation of Bdp1-deficient cell models for investigation of TFIIIB″ 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.