
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Dnmt3a CRISPR Activation Plasmid (m) | sc-420035-ACT | 20 µg | $397.00 |
Mouse Dnmt3a encodes a de novo DNA methyltransferase that establishes CpG methylation patterns during development and cell fate commitment, shaping chromatin accessibility and long-term transcriptional programs. DNMT3A cooperates with DNMT3B and DNMT1 to maintain epigenetic memory, linking DNA methylation to histone modification networks and transcriptional repression. Its activity influences differentiation, genomic imprinting, and transposon silencing, and dysregulation of DNMT3A-dependent methylation is associated with altered lineage specification and epigenetic instability in disease models. Dnmt3a is therefore widely studied in pathways governing stem cell biology, hematopoietic regulation, and methylation-dependent control of gene expression.
Dnmt3a CRISPR Activation Plasmid (m) provides a targeted, non-destructive approach to upregulating endogenous Dnmt3a expression without altering the underlying DNA sequence.
Dnmt3a CRISPR Activation Plasmid (m) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the Dnmt3a 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 Dnmt3a transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Dnmt3a expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native Dnmt3a locus and enabling the study of Dnmt3a-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Dnmt3a pathway restoration in tumor cells with silenced or reduced Dnmt3a expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.