
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Limkain b1 CRISPR Activation Plasmid (h) | sc-411308-ACT | 20 µg | $397.00 | |||
Limkain b1 CRISPR Activation Plasmid (h2) | sc-411308-ACT-2 | 20 µg | $397.00 |
KIAA0430 encodes Limkain b1, a human protein implicated in cytoskeletal organization and actin-associated processes that shape cell morphology, adhesion, and motility. Studies of Limkain family proteins suggest links to signaling pathways that couple membrane dynamics to actin remodeling, supporting coordinated changes in cellular architecture. Altered regulation of actin-cytoskeleton networks is frequently associated with dysregulated proliferation, migration, and invasion phenotypes in cancer and with impaired neuronal connectivity in neurodevelopmental contexts. Characterizing Limkain b1 expression and function can help clarify how cytoskeletal control interfaces with broader transcriptional and signaling programs relevant to disease-associated cell-state transitions.
Limkain b1 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous KIAA0430 expression without altering the underlying DNA sequence.
Limkain b1 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the KIAA0430 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 KIAA0430 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous Limkain b1 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native KIAA0430 locus and enabling the study of Limkain b1-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of Limkain b1 pathway restoration in tumor cells with silenced or reduced KIAA0430 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.