
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
γ1 Tubulin CRISPR Activation Plasmid (h) | sc-400327-ACT | 20 µg | $397.00 |
TUBG1 encodes human γ1 tubulin, a core component of the γ-tubulin ring complex that nucleates microtubules at centrosomes and other microtubule-organizing centers. By supporting mitotic spindle assembly, centrosome integrity, and cell-cycle progression, γ1 tubulin helps coordinate chromosome segregation and faithful cell division. TUBG1-dependent microtubule dynamics intersect with pathways governing cytoskeletal organization, intracellular trafficking, and neurodevelopmental processes requiring precise centrosome function. Dysregulation of microtubule nucleation and spindle mechanics is relevant to genomic instability and proliferative phenotypes, making TUBG1 a useful node for studying cell-division–linked disease biology.
γ1 Tubulin CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous TUBG1 expression without altering the underlying DNA sequence.
γ1 Tubulin CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the TUBG1 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 TUBG1 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous γ1 Tubulin expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native TUBG1 locus and enabling the study of γ1 Tubulin-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of γ1 Tubulin pathway restoration in tumor cells with silenced or reduced TUBG1 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.