
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
BAZ2B CRISPR Activation Plasmid (m) | sc-436575-ACT | 20 µg | $397.00 | |||
BAZ2B CRISPR Activation Plasmid (m2) | sc-436575-ACT-2 | 20 µg | $397.00 |
Mouse Baz2b encodes BAZ2B, a bromodomain-containing chromatin regulator that interprets acetyl-lysine marks on histones and helps coordinate nucleosome remodeling and transcriptional control. Through its role in chromatin accessibility and epigenetic regulation, BAZ2B can influence developmental gene programs, cell identity maintenance, and stimulus-responsive transcriptional networks. Altered bromodomain-mediated signaling and dysregulated chromatin remodeling are broadly linked to mechanisms relevant to neurodevelopment, metabolic homeostasis, and oncogenic transcriptional states, making Baz2b a useful node for probing epigenetic pathway interactions. Experimental modulation of Baz2b expression supports studies of promoter/enhancer function, chromatin-dependent transcription, and gene network rewiring in mammalian systems.
BAZ2B CRISPR Activation Plasmid (m) provides a targeted, non-destructive approach to upregulating endogenous Baz2b expression without altering the underlying DNA sequence.
BAZ2B CRISPR Activation Plasmid (m) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the Baz2b 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 Baz2b transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous BAZ2B expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native Baz2b locus and enabling the study of BAZ2B-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of BAZ2B pathway restoration in tumor cells with silenced or reduced Baz2b expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.