
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
ST5 CRISPR Activation Plasmid (h) | sc-411020-ACT | 20 µg | $397.00 |
Human ST5 (suppression of tumorigenicity 5) encodes a multi-domain adaptor protein that modulates intracellular signal transduction and cytoskeletal-associated processes. ST5 has been reported to interact with components of RAS/MAPK signaling and other growth factor–responsive pathways, influencing cellular proliferation, differentiation, and stress responses in a context-dependent manner. Altered ST5 expression or pathway coupling has been observed in several cancer-related and neurobiological research settings, linking it to dysregulated mitogenic signaling and cellular homeostasis. As a result, ST5 is frequently studied for its role in signal integration, pathway cross-talk, and phenotype modulation in human cell models.
ST5 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous ST5 expression without altering the underlying DNA sequence.
ST5 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the ST5 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 ST5 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous ST5 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native ST5 locus and enabling the study of ST5-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of ST5 pathway restoration in tumor cells with silenced or reduced ST5 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.