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.
Rictor CRISPR Activation Plasmid (h): sc-400710-ACT
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- Rictor CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- Rictor 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 Rictor CRISPR Activation Plasmid (h) and Rictor CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the RICTOR transcriptional start site. One or both designs may be available
- Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: Rictor Antibody (H-11): sc-271081
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Rictor CRISPR Activation Plasmid (h) | sc-400710-ACT | 20 µg | $397.00 | |||
Rictor CRISPR Activation Plasmid (h2) | sc-400710-ACT-2 | 20 µg | $397.00 |
RICTOR encodes Rictor, an essential scaffold component of mTOR complex 2 (mTORC2) that coordinates kinase signaling to regulate cell survival, proliferation, metabolism, and cytoskeletal organization. Through mTORC2-dependent phosphorylation of AGC family kinases, including AKT (Ser473), SGK, and PKC isoforms, Rictor contributes to PI3K–AKT pathway tuning, insulin signaling, and actin dynamics. Altered RICTOR expression or mTORC2 activity is frequently associated with dysregulated growth factor signaling and metabolic reprogramming observed across diverse cancer and metabolic disease contexts. As a central node in nutrient and growth factor sensing, Rictor is widely studied in mechanisms of drug resistance, migration, and lineage-specific differentiation.
Rictor CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous RICTOR expression without altering the underlying DNA sequence.
Rictor CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the RICTOR 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 RICTOR transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Rictor expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native RICTOR locus and enabling the study of Rictor-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Rictor pathway restoration in tumor cells with silenced or reduced RICTOR expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.