
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Gfi-1B CRISPR Activation Plasmid (h) | sc-403883-ACT | 20 µg | $397.00 |
GFI1B encodes the transcriptional repressor Gfi-1B, a zinc-finger protein that is essential for hematopoietic development and lineage specification, particularly within erythroid and megakaryocytic programs. Through interactions with chromatin-modifying complexes such as LSD1/RCOR/HDAC, Gfi-1B shapes transcriptional networks that govern progenitor proliferation, differentiation, and maturation. Its activity integrates with core hematopoietic regulators to control gene expression programs involved in platelet formation and red blood cell development. Dysregulated GFI1B expression or function has been associated with inherited platelet disorders and broader perturbations of hematopoietic homeostasis relevant to blood cell malignancy research.
Gfi-1B CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous GFI1B expression without altering the underlying DNA sequence.
Gfi-1B CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the GFI1B 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 GFI1B transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Gfi-1B expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native GFI1B locus and enabling the study of Gfi-1B-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Gfi-1B pathway restoration in tumor cells with silenced or reduced GFI1B expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.