
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
KIAA0947 CRISPR Activation Plasmid (h) | sc-411728-ACT | 20 µg | $397.00 |
Human ICE1 (also known as KIAA0947) encodes a nuclear regulatory protein implicated in transcriptional control and cellular stress-responsive programs. ICE1-associated activity has been linked to chromatin-dependent regulation of gene expression and coordination of signaling outputs that influence cell-cycle progression and differentiation state. Altered expression or network connectivity of ICE1/KIAA0947 has been observed across multiple disease-relevant contexts, supporting its use as a node for probing dysregulated transcriptional circuitry in complex phenotypes. As a research target, ICE1/KIAA0947 is useful for dissecting pathway-level effects of endogenous gene upregulation on downstream transcriptomes.
KIAA0947 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous ICE1 expression without altering the underlying DNA sequence.
KIAA0947 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the ICE1 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 ICE1 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous KIAA0947 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native ICE1 locus and enabling the study of KIAA0947-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of KIAA0947 pathway restoration in tumor cells with silenced or reduced ICE1 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.