
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
MOB2 CRISPR Activation Plasmid (h) | sc-413424-ACT | 20 µg | $397.00 |
Human MOB2 (MOB kinase activator 2) encodes a conserved adaptor protein that binds NDR1/2 (STK38/STK38L) family kinases and helps regulate their activation state within Hippo-related signaling networks. Through these interactions, MOB2 contributes to control of cell cycle progression, cytoskeletal organization, polarity, and stress-responsive signaling that collectively influence proliferation and migration. Dysregulation of NDR/Hippo axis components is frequently associated with altered growth control and genomic stability, making MOB2 a relevant node for studying pathway wiring in cancer biology and other disorders of tissue homeostasis. MOB2 also provides a mechanistic entry point to investigate kinase-dependent transcriptional programs and phospho-signaling dynamics in human cell models.
MOB2 CRISPR Activation Plasmid (h) provides a targeted, non-destructive approach to upregulating endogenous MOB2 expression without altering the underlying DNA sequence.
MOB2 CRISPR Activation Plasmid (h) is a three-plasmid synergistic activation mediator (SAM) system engineered for highly efficient, site-specific transcriptional upregulation of the MOB2 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 MOB2 transcriptional start site, where VP64, p65, and HSF1 act in concert to recruit transcriptional machinery and drive upregulation of endogenous MOB2 expression. Unlike nuclease-active Cas9, dCas9 does not introduce double-strand breaks or modify the genomic sequence, preserving the native MOB2 locus and enabling the study of MOB2-dependent transcriptional responses at the endogenous locus, making it a valuable tool for functional studies, target gene identification, and the modeling of MOB2 pathway restoration in tumor cells with silenced or reduced MOB2 expression.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.