Ski CRISPR Activation Plasmid (m): sc-422964-ACT
- Target species: mouse
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- Ski CRISPR Activation Plasmid (m) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- Ski CRISPR Activation Plasmid (m) 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 Ski CRISPR Activation Plasmid (m) and Ski CRISPR Activation Plasmid (m2) target distinct regulatory regions upstream of the Ski 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: Ski Antibody (G8): sc-33693
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Ski CRISPR Activation Plasmid (m) | sc-422964-ACT | 20 µg | $397.00 | |||
Ski CRISPR Activation Plasmid (m2) | sc-422964-ACT-2 | 20 µg | $397.00 |
Mouse Ski (Sloan-Kettering viral oncogene homolog) encodes a nuclear transcriptional regulator that modulates gene expression programs controlling proliferation, differentiation, and lineage commitment. SKI is best known as a negative regulator of TGF-β/SMAD signaling, where it can repress SMAD-dependent transcription and influence epithelial–mesenchymal transition, extracellular matrix remodeling, and immune-related transcriptional outputs. Through crosstalk with pathways such as BMP signaling and chromatin-associated co-regulators, SKI impacts developmental patterning and tissue homeostasis. Altered SKI expression or activity has been implicated in phenotypes relevant to fibrosis, cancer biology, and craniofacial or skeletal development, making it a useful node for mechanistic pathway studies.
Ski CRISPR Activation Plasmid (m) provides a targeted, non-destructive approach to upregulating endogenous Ski expression without altering the underlying DNA sequence.
Ski CRISPR Activation Plasmid (m) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the Ski 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 Ski transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Ski expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native Ski locus and enabling the study of Ski-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Ski pathway restoration in tumor cells with silenced or reduced Ski expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.