
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
TCP-1 γ CRISPR/Cas9 KO Plasmid (h) | sc-403203 | 20 µg | $397.00 |
CCT3 encodes the human chaperonin-containing TCP-1 subunit gamma (TCP-1 γ), a core component of the cytosolic TRiC/CCT complex that drives ATP-dependent folding of a broad set of client proteins. TRiC/CCT supports proteostasis by assisting maturation of cytoskeletal proteins such as actin and tubulin and by influencing folding and stability of signaling and cell-cycle regulators. Through these roles, TCP-1 γ contributes to cytoskeleton organization, protein quality control, and proliferative capacity, with perturbations in chaperonin function linked to proteotoxic stress and altered growth signaling. Dysregulated CCT subunit expression has been reported across multiple disease contexts, supporting its study in pathways relevant to oncogenic transformation and neurodegeneration-associated protein misfolding.
TCP-1 γ CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CCT3 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CCT3 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 CCT3 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 TCP-1 γ protein expression.
This CRISPR knockout system enables efficient generation of CCT3-deficient cell models for investigation of TCP-1 γ 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.