ALMS1 CRISPR Activation Plasmid (h): sc-407355-ACT
- Target species: human
- 20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
- ALMS1 CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
- ALMS1 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 ALMS1 CRISPR Activation Plasmid (h) and ALMS1 CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the ALMS1 transcriptional start site. One or both designs may be available
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
ALMS1 CRISPR Activation Plasmid (h) | sc-407355-ACT | 20 µg | $397.00 |
ALMS1 encodes a large centrosomal and basal body–associated protein that localizes to primary cilia and is required for ciliogenesis, ciliary trafficking, and maintenance of microtubule organization. Through its role in cilia-dependent signaling, ALMS1 influences pathways such as Hedgehog and other sensory transduction programs that coordinate cell-cycle control, polarity, and tissue homeostasis. Disruption of ALMS1 function is linked to ciliopathy phenotypes, including Alström syndrome, and is widely studied in the context of metabolic dysregulation, retinal degeneration, cardiomyopathy, and renal dysfunction. Modulating ALMS1 expression is therefore useful for dissecting ciliary biology, intracellular transport, and signaling networks underlying multisystem disease mechanisms.
ALMS1 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous ALMS1 expression without altering the underlying DNA sequence.
ALMS1 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the ALMS1 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 ALMS1 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous ALMS1 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native ALMS1 locus and enabling the study of ALMS1-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of ALMS1 pathway restoration in tumor cells with silenced or reduced ALMS1 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.