
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Med28 CRISPR Activation Plasmid (h) | sc-407371-ACT | 20 µg | $397.00 |
Human MED28 encodes Med28, a Mediator complex subunit that contributes to RNA polymerase II–dependent transcription and coordinates signal-responsive gene expression programs. Med28 has been linked to regulation of cell adhesion and cytoskeletal dynamics through interactions that connect transcriptional control with pathways such as MAPK/ERK and integrin-associated signaling. Altered MED28 expression has been reported across multiple cancer-related datasets and is studied for its relationship to proliferation, migration, and stress-adaptive transcriptional states. As a transcriptional co-regulator, Med28 provides a useful entry point for dissecting Mediator-dependent control of gene networks in development and disease models.
Med28 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous MED28 expression without altering the underlying DNA sequence.
Med28 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the MED28 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 MED28 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Med28 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native MED28 locus and enabling the study of Med28-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Med28 pathway restoration in tumor cells with silenced or reduced MED28 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.