
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Pericentrin 2 CRISPR Activation Plasmid (h) | sc-401822-ACT | 20 µg | $397.00 |
PCNT encodes pericentrin 2, a core pericentriolar material scaffold essential for centrosome maturation and microtubule nucleation. By organizing γ-tubulin ring complexes and anchoring regulatory proteins such as AURKA and PLK1, pericentrin 2 supports mitotic spindle assembly, chromosome segregation, and ciliogenesis. Disruption of PCNT-dependent centrosomal architecture perturbs cell-cycle control and genomic stability, processes frequently implicated in developmental disorders and cancer-associated aneuploidy. Because centrosome integrity influences signaling outputs from the primary cilium, PCNT is also relevant to studies of cilia-linked signaling pathways and cellular polarity.
Pericentrin 2 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous PCNT expression without altering the underlying DNA sequence.
Pericentrin 2 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the PCNT locus in human cell lines. The system is built around a catalytically inactive Cas9 (dCas9) carrying two inactivating mutations (D10A and N863A) that eliminate nuclease activity while preserving DNA binding. This dCas9 is fused to VP64, a potent transcriptional activator, and is co-expressed with a blasticidin resistance gene for selection. The second plasmid encodes the MS2-p65-HSF1 fusion protein, a secondary activator complex that works in concert with dCas9-VP64, alongside a hygromycin resistance gene. The third plasmid encodes a target-specific 20 nt sgRNA fused to two MS2 RNA aptamers that recruit the MS2-p65-HSF1 complex to the activation site, accompanied by a puromycin resistance gene. The three plasmids are delivered at a 1:1:1 mass ratio for balanced expression of all system components.
Once assembled at the target locus, the SAM complex binds within approximately 200 bp upstream of the PCNT transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Pericentrin 2 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native PCNT locus and enabling the study of Pericentrin 2-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Pericentrin 2 pathway restoration in tumor cells with silenced or reduced PCNT expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.