ST CRISPR Activation Plasmid (h): sc-400733-ACT
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- ST CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- ST 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 ST CRISPR Activation Plasmid (h) and ST CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the SLC6A4 transcriptional start site. One or both designs may be available
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
ST CRISPR Activation Plasmid (h) | sc-400733-ACT | 20 µg | $397.00 |
SLC6A4 encodes the sodium- and chloride-dependent serotonin transporter (ST, also known as SERT), a plasma membrane symporter that terminates serotonergic signaling by reuptake of 5-hydroxytryptamine from the extracellular space. By regulating serotonin availability, ST shapes neurotransmission, synaptic plasticity, and downstream signaling networks linked to cAMP/PKA and MAPK-dependent transcriptional responses. In addition to neuronal cells, SLC6A4 activity influences peripheral serotonergic processes in platelets and gastrointestinal tissues that intersect with neuroimmune and stress-response pathways. Altered SLC6A4 expression or function is associated with susceptibility to neuropsychiatric and behavioral phenotypes, making it a relevant target for mechanistic studies of serotonergic circuit regulation.
ST CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous SLC6A4 expression without altering the underlying DNA sequence.
ST CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the SLC6A4 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 SLC6A4 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous ST expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native SLC6A4 locus and enabling the study of ST-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of ST pathway restoration in tumor cells with silenced or reduced SLC6A4 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.