
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Lefty-A CRISPR Activation Plasmid (h) | sc-403932-ACT | 20 µg | $397.00 |
Human LEFTY2 encodes Lefty-A, a secreted TGF-β superfamily antagonist that modulates NODAL/Activin signaling through competitive interactions with receptor complexes and related extracellular regulators. By constraining SMAD2/3 pathway activity, Lefty-A contributes to feedback control of mesendoderm specification, left–right axis patterning, and broader developmental signaling homeostasis. Dysregulated LEFTY2 expression has been associated with aberrant morphogen gradients and altered cellular differentiation programs, and it is frequently examined in contexts involving epithelial–mesenchymal transitions and tumor-associated signaling rewiring. As a result, LEFTY2 serves as a useful node for dissecting TGF-β–related pathway dynamics and transcriptional network states in human model systems.
Lefty-A CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous LEFTY2 expression without altering the underlying DNA sequence.
Lefty-A CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the LEFTY2 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 LEFTY2 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Lefty-A expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native LEFTY2 locus and enabling the study of Lefty-A-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Lefty-A pathway restoration in tumor cells with silenced or reduced LEFTY2 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.