
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
LGR6 CRISPR Activation Plasmid (h) | sc-401443-ACT | 20 µg | $397.00 |
Human LGR6 encodes a leucine-rich repeat–containing G protein-coupled receptor that functions as a high-affinity receptor for R-spondins and potentiates canonical Wnt/β-catenin signaling. By enhancing Wnt-driven transcriptional programs, LGR6 contributes to regulation of epithelial stem/progenitor cell maintenance, tissue homeostasis, and differentiation dynamics. LGR6 activity intersects with pathways governing cell cycle control, migration, and regenerative responses, making it a useful node for studying signaling crosstalk in development and remodeling. Dysregulated LGR6–R-spondin–Wnt axis signaling has been associated with oncogenic pathway activation and altered stem-like states, supporting investigation of LGR6 in cancer biology and related signaling phenotypes.
LGR6 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous LGR6 expression without altering the underlying DNA sequence.
LGR6 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the LGR6 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 LGR6 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous LGR6 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native LGR6 locus and enabling the study of LGR6-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of LGR6 pathway restoration in tumor cells with silenced or reduced LGR6 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.