Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
IP3R-III CRISPR Activation Plasmid (h): sc-402138-ACT
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- IP3R-III CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- IP3R-III CRISPR Activation Plasmid (h) consists of three plasmids at a 1:1:1 mass ratio: a plasmid encoding the deactivated Cas9 (dCas9) nuclease (D10A and N863A) fused to the transactivation domain VP64, and a blasticidin resistance gene; a plasmid encoding the MS2-p65-HSF1 fusion protein, and a hygromycin resistance gene; a plasmid encoding a target-specific 20 nt guide RNA fused to two MS2 RNA aptamers, and a puromycin resistance gene
- The resulting SAM complex binds to a site-specific region approximately 200-250 nt upstream of the transcriptional start site and provides robust recruitment of transcription factors for highly efficient gene activation
- gRNAs encoded by IP3R-III CRISPR Activation Plasmid (h) and IP3R-III CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the ITPR3 transcriptional start site. One or both designs may be available
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
IP3R-III CRISPR Activation Plasmid (h) | sc-402138-ACT | 20 µg | $397.00 |
ITPR3 encodes inositol 1,4,5-trisphosphate receptor type 3 (IP3R-III), an endoplasmic reticulum Ca²⁺ release channel that opens in response to IP3 generated downstream of phospholipase C signaling. By shaping intracellular Ca²⁺ oscillations and microdomain signaling, IP3R-III regulates secretion, epithelial polarity, mitochondrial metabolism, and Ca²⁺-dependent transcriptional programs. IP3R-III function intersects with GPCR and receptor tyrosine kinase pathways, coupling extracellular cues to ER Ca²⁺ dynamics and downstream effectors such as calmodulin-dependent kinases and NFAT signaling. Altered ITPR3 expression or Ca²⁺ homeostasis has been associated with dysregulated proliferation, stress responses, and epithelial remodeling in multiple disease-relevant contexts, supporting mechanistic studies of Ca²⁺ signaling networks.
IP3R-III CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous ITPR3 expression without altering the underlying DNA sequence.
IP3R-III CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the ITPR3 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 ITPR3 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous IP3R-III expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native ITPR3 locus and enabling the study of IP3R-III-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of IP3R-III pathway restoration in tumor cells with silenced or reduced ITPR3 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.