
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
BORIS CRISPR Activation Plasmid (h) | sc-403313-ACT | 20 µg | $397.00 |
CTCFL encodes BORIS (Brother of the Regulator of Imprinted Sites), a cancer-testis DNA-binding protein related to CTCF that recognizes insulator-like sequences and reshapes chromatin architecture. BORIS participates in epigenetic regulation of transcription through modulation of promoter/enhancer activity, DNA methylation states, and higher-order genome organization, influencing processes such as germline gene expression, cell fate programs, and chromatin accessibility. Aberrant BORIS expression is linked to transcriptional reprogramming and dysregulated expression of normally silenced germline and oncogenic networks, making it a useful target for studying epigenetic plasticity and transcriptional control mechanisms in human cells.
BORIS CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous CTCFL expression without altering the underlying DNA sequence.
BORIS CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the CTCFL 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 CTCFL transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous BORIS expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native CTCFL locus and enabling the study of BORIS-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of BORIS pathway restoration in tumor cells with silenced or reduced CTCFL expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.