SEMA3E Lentiviral Activation Particles (h): sc-404797-LAC
- Target species: human
- 200 µl of transduction-ready, high-titer CRISPR/dCas9 Lentiviral Activation Particles
- SEMA3E Lentiviral Activation Particles (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically and efficiently upregulate gene expression via lentiviral transduction of cells
- SEMA3E Lentiviral Activation Particles (h) contain the following SAM Activation elements: a deactivated Cas9 (dCas9) nuclease (D10A and N863A) fused to the transactivation domain VP64, an MS2-p65-HSF1 fusion protein and a target-specific 20 nt guide RNA. They also contain the blasticidin, hygromycin and puromycin resistance genes
- Upon transduction, the SAM complex binds to a site-specific region approximately 200-250 nt upstream of the transcriptional start site and provides robust recruitment of transcription factors for highly efficient gene activation
- gRNAs encoded by SEMA3E Lentiviral Activation Plasmid (h) and SEMA3E Lentiviral Activation Plasmid (h2) target distinct regulatory regions of the SEMA3E promoter. One or both designs may be available
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
SEMA3E Lentiviral Activation Particles (h) | sc-404797-LAC | 200 µl | $455.00 |
SEMA3E encodes semaphorin-3E, a secreted guidance cue that signals primarily through plexin receptors to regulate cytoskeletal remodeling, directional cell migration, and cell–cell interactions. In human cells, SEMA3E influences axon guidance, vascular patterning, and epithelial organization by modulating Rho family GTPase signaling and downstream pathways that control adhesion and motility. Dysregulated SEMA3E signaling has been linked to altered angiogenic responses and invasive phenotypes in multiple cancer contexts, and it is also studied in neurodevelopmental and inflammatory processes. These properties make SEMA3E a useful target for dissecting mechanisms of microenvironmental signaling, migration circuits, and receptor-mediated guidance programs.
SEMA3E Lentiviral Activation Particles (h) address this need by packaging the complete synergistic activation mediator (SAM) transcriptional activation system into transduction-ready, high-titer lentiviral particles, enabling efficient SEMA3E upregulation across a broader range of human cell types.
SEMA3E Lentiviral Activation Particles (h) deliver all functional components of the synergistic activation mediator (SAM) system via lentiviral transduction. The system comprises three particle preparations co-transduced into target cells: one encoding catalytically inactive dCas9 (D10A and N863A mutations) fused to the VP64 transactivation domain with a blasticidin resistance gene; one encoding the MS2-p65-HSF1 fusion protein with a hygromycin resistance gene; and one encoding a target-specific 20 nt sgRNA fused to two MS2 RNA aptamers with a puromycin resistance gene. Following lentiviral transduction and genomic integration of the expression cassettes, the SAM components are stably expressed and assemble at the target locus within the proximal promoter region upstream of the SEMA3E transcriptional start site, where VP64, p65, and HSF1 act cooperatively to recruit endogenous transcriptional machinery and drive sustained upregulation of endogenous SEMA3E expression. The use of nuclease-inactive dCas9 avoids the introduction of double-strand DNA breaks and preserves the native SEMA3E genomic locus and regulatory architecture.
The lentiviral format offers several practical advantages: stable genomic integration supports heritable activation across cell divisions; high-titer particle preparations eliminate the need for in-house viral production; and compatibility with primary, non-dividing, and transfection-resistant cell types expands experimental accessibility. Successful transduction can be confirmed and enriched through triple antibiotic selection using puromycin, hygromycin, and blasticidin.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.