
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Histone Deacetylase 2 (HDAC2) CRISPR/Cas9 KO Plasmid (r) | sc-437286 | 20 µg | $397.00 |
Histone deacetylase 2 (HDAC2) is a class I Zn²⁺-dependent histone deacetylase that removes acetyl groups from lysine residues on histones and other nuclear proteins, promoting chromatin compaction and transcriptional repression. In rat cells, HDAC2 functions within corepressor assemblies such as Sin3, NuRD, and CoREST to coordinate gene-expression programs controlling cell-cycle progression, differentiation, synaptic plasticity, and DNA damage responses. Through crosstalk with signaling networks including MAPK/ERK, PI3K-AKT, and p53-dependent checkpoints, HDAC2 contributes to context-specific regulation of proliferation and stress adaptation. Dysregulated HDAC2 activity has been associated with altered inflammatory gene expression and epigenetic remodeling relevant to neurobiology and oncogenic transformation, making it a frequent target in mechanistic studies of chromatin-driven phenotypes.
Histone Deacetylase 2 (HDAC2) CRISPR/Cas9 KO Plasmid (r) is a pool of plasmids designed for targeted disruption of the gene in rat cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the 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 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 Histone Deacetylase 2 (HDAC2) protein expression.
This CRISPR knockout system enables efficient generation of -deficient cell models for investigation of Histone Deacetylase 2 (HDAC2) 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.