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.
VGAT CRISPR Activation Plasmid (h): sc-401850-ACT
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- VGAT CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- VGAT 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 VGAT CRISPR Activation Plasmid (h) and VGAT CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the SLC32A1 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: VGAT Antibody (F-2): sc-393373
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
VGAT CRISPR Activation Plasmid (h) | sc-401850-ACT | 20 µg | $397.00 |
SLC32A1 encodes vesicular GABA transporter (VGAT), a synaptic vesicle membrane protein that loads GABA and glycine into secretory vesicles to enable inhibitory neurotransmission. By controlling vesicular uptake and quantal size, VGAT regulates excitation–inhibition balance, synaptic plasticity, and neuronal network oscillations across the central nervous system. Altered inhibitory signaling linked to dysregulated SLC32A1/VGAT activity is relevant to studies of epilepsy, anxiety-related phenotypes, neurodevelopmental disorders, and movement disorders, where circuit-level inhibition is perturbed. As a vesicular transporter, VGAT function intersects with synaptic vesicle cycling, neurotransmitter metabolism, and ion-gradient–dependent transport processes that shape inhibitory synapse efficacy.
VGAT CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous SLC32A1 expression without altering the underlying DNA sequence.
VGAT CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the SLC32A1 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 SLC32A1 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous VGAT expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native SLC32A1 locus and enabling the study of VGAT-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of VGAT pathway restoration in tumor cells with silenced or reduced SLC32A1 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.