
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
RbAp46 CRISPR/Cas9 KO Plasmid (h) | sc-405076 | 20 µg | $397.00 |
RBBP7 encodes RbAp46, a WD40 repeat histone-binding protein that functions as a core component of multiple chromatin regulatory complexes, including NuRD/HDAC, Sin3A, and PRC2, and associates with CAF-1 during nucleosome assembly. Through these interactions, RbAp46 helps coordinate histone deacetylation, chromatin remodeling, and epigenetic gene silencing, impacting transcriptional programs, DNA replication-coupled chromatin assembly, and genome stability. Altered RBBP7-dependent chromatin regulation has been linked to dysregulated proliferation, differentiation defects, and stress-response phenotypes observed across cancer and developmental disease contexts. As a nodal chromatin factor, RbAp46 is frequently studied in pathways controlling cell cycle progression, DNA damage responses, and lineage-specific transcription.
RbAp46 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the RBBP7 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the RBBP7 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 RBBP7 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 RbAp46 protein expression.
This CRISPR knockout system enables efficient generation of RBBP7-deficient cell models for investigation of RbAp46 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.