Date published: 2026-7-13

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ETBR Lentiviral Activation Particles (m): sc-420112-LAC

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Datasheets
  • Target species: mouse
  • 200 µl of transduction-ready, high-titer CRISPR/dCas9 Lentiviral Activation Particles
  • ETBR Lentiviral Activation Particles (m) is a synergistic activation mediator (SAM) transcription activation system designed to specifically and efficiently upregulate gene expression via lentiviral transduction of cells
  • ETBR Lentiviral Activation Particles (m) 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 ETBR Lentiviral Activation Plasmid (m) and ETBR Lentiviral Activation Plasmid (m2) target distinct regulatory regions of the Ednrb promoter. One or both designs may be available
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    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    ETBR Lentiviral Activation Particles (m)

    sc-420112-LAC
    200 µl
    $455.00

    Mouse Ednrb encodes endothelin receptor type B (ETBR), a class A GPCR that binds endothelin peptides to regulate vasomotor signaling, neural crest–derived lineage development, and melanocyte and enteric nervous system maturation. ETBR couples primarily to G proteins that engage PLC/IP3–Ca2+ signaling, MAPK cascades, and nitric oxide–related pathways, shaping cell migration, proliferation, and differentiation in a context-dependent manner. Ednrb activity is tightly linked to patterning processes and pigment cell biology, and disruption of endothelin signaling through ETBR is associated with defects in enteric innervation and melanocyte function. As a result, Ednrb is widely used as a mechanistic node to study GPCR signaling dynamics, neural crest development, and cell-type–specific transcriptional programs in mouse models.

    ETBR Lentiviral Activation Particles (m) address this need by packaging the complete synergistic activation mediator (SAM) transcriptional activation system into transduction-ready, high-titer lentiviral particles, enabling efficient Ednrb upregulation across a broader range of human cell types.

    ETBR Lentiviral Activation Particles (m) 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 Ednrb transcriptional start site, where VP64, p65, and HSF1 act cooperatively to recruit endogenous transcriptional machinery and drive sustained upregulation of endogenous ETBR expression. The use of nuclease-inactive dCas9 avoids the introduction of double-strand DNA breaks and preserves the native Ednrb 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.