
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
connexin 37 CRISPR Activation Plasmid (m) | sc-420559-ACT | 20 µg | $397.00 | |||
connexin 37 CRISPR Activation Plasmid (m2) | sc-420559-ACT-2 | 20 µg | $397.00 |
Mouse Gja4 encodes connexin 37 (Cx37), a gap junction channel subunit that assembles into connexons to mediate direct intercellular communication via ions and small metabolites. Cx37-dependent coupling helps coordinate endothelial function, vascular tone, and smooth muscle–endothelial signaling, influencing processes such as shear stress responses, cell-cycle control, and tissue homeostasis. In the vasculature and lymphatic system, altered connexin-mediated signaling has been linked to dysregulated angiogenesis, inflammation, and vascular remodeling, making Gja4 a useful locus for studying mechanisms underlying cardiovascular and lymphatic phenotypes. Because gap junction composition shapes signal propagation between neighboring cells, Gja4 modulation is also relevant to investigations of barrier integrity and microenvironmental control of cell behavior.
connexin 37 CRISPR Activation Plasmid (m) provides a targeted, non-destructive approach to upregulating endogenous Gja4 expression without altering the underlying DNA sequence.
connexin 37 CRISPR Activation Plasmid (m) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the Gja4 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 Gja4 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous connexin 37 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native Gja4 locus and enabling the study of connexin 37-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of connexin 37 pathway restoration in tumor cells with silenced or reduced Gja4 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.