
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
NEDL2 Lentiviral Activation Particles (h) | sc-410607-LAC | 200 µl | $455.00 |
Human HECW2 encodes NEDL2, a HECT-type E3 ubiquitin-protein ligase that regulates proteostasis by catalyzing ubiquitin transfer to specific substrates, thereby influencing their stability, localization, and signaling output. NEDL2 is implicated in control of neuronal development and synaptic function through ubiquitin-dependent modulation of pathways governing protein turnover, cytoskeletal dynamics, and transcriptional programs. Perturbation of HECW2/NEDL2 has been linked to neurodevelopmental phenotypes, making it a relevant node for studying how ubiquitination shapes cellular signaling networks. In biomedical research, HECW2 provides a mechanistic entry point to interrogate ubiquitin-mediated regulation in neuronal and other cell contexts, including downstream effects on gene expression and stress-response circuitry.
NEDL2 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 HECW2 upregulation across a broader range of human cell types.
NEDL2 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 HECW2 transcriptional start site, where VP64, p65, and HSF1 act cooperatively to recruit endogenous transcriptional machinery and drive sustained upregulation of endogenous NEDL2 expression. The use of nuclease-inactive dCas9 avoids the introduction of double-strand DNA breaks and preserves the native HECW2 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.