BRE Reporter Lentivirus

SKU:BHV19400070
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    Overview
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    The BRE Reporter Lentivirus provides a stable fluorescent or luminescent readout of BMP signaling pathway activity through BMP response elements bound by the SMAD1/5/8-SMAD4 complex. Purified by PEG precipitation and sucrose gradient centrifugation, it efficiently transduces primary and thawed cells to establish reporter cell lines for studying BMP signaling in development, stem cell differentiation, and tissue homeostasis.
    Species Human, Mouse
    Pathway Target BMP
    Reporter d2GFP, EGFP, Firefly Luc (+4 more)
    Selection Blasticidin, Puromycin
    Promoter EF1a
    Titer 3×10⁸ VP/mL
    Format 3rd Gen, VSV-G Pseudotyped
    Available Options

    Select the lentiviral variant that best fits your experiment. Availability and lead time may vary by option.

    • Options:
      • Promoter+Reporter: Selection-Puromycin; Selection: Puromycin; Amount (TU): 5x10^6 — BRE Reporter Lentivirus: Selection-Puromycin format with Puromycin selection; supplied as 5x10^6 TU.
      • Promoter+Reporter: Selection-Blasticidin; Selection: Blasticidin; Amount (TU): 5x10^6 — BRE Reporter Lentivirus: Selection-Blasticidin format with Blasticidin selection; supplied as 5x10^6 TU.
      • Promoter+Reporter: Selection-Puromycin; Selection: Puromycin; Amount (TU): 2x10^6 — BRE Reporter Lentivirus: Selection-Puromycin format with Puromycin selection; supplied as 2x10^6 TU.
      • Promoter+Reporter: Selection-Blasticidin; Selection: Blasticidin; Amount (TU): 2x10^6 — BRE Reporter Lentivirus: Selection-Blasticidin format with Blasticidin selection; supplied as 2x10^6 TU.
    • Lead time: typically ships in ~7 business days; timing may vary by selected option.
    • Storage: store at -80°C
    • Shipping: Ships on dry ice
    • Upon receipt: follow the product datasheet storage instructions.
    • Sales terms and conditions: Please review prior to ordering.
    Options selector
    Catalog no. Reporter Selection Amount (TU)
    LTV-0075-1S GFP
    LTV-0075-2S RFP
    LTV-0075-3S Firefly Luc
    Field Specification
    Product Type
    • Lentiviral Vector
    • TF Reporter Lentivirus
    Promoter EF1a
    Reporter d2GFP, EGFP, Firefly Luc, GFP, mCherry, RFP, β-Galactosidase
    Selection Marker Blasticidin, Puromycin
    Shipping Ships on dry ice; store at -80°C
    Species Human, Mouse

    Background

    Bone morphogenetic proteins (BMPs) are members of the TGF-β superfamily that signal through type I and type II serine/threonine kinase receptors. Ligand binding activates the receptor-regulated SMADs (SMAD1, SMAD5, and SMAD8), which form a complex with the common mediator SMAD4 and accumulate in the nucleus, where they bind BMP response elements (BRE) to regulate target gene transcription. BMP signaling controls embryogenesis, skeletal and organ development, stem cell fate, and adult tissue homeostasis. Dysregulated BMP signaling is associated with skeletal disorders, fibrosis, and cancer, making BRE-driven reporters useful tools for studying this pathway.

    Product Description & Applications

    The BRE Reporter Lentivirus is a transcription factor reporter system that provides a sensitive fluorescent or luminescent readout of BMP signaling pathway activity in mammalian cells. The construct contains inverted repeats of BMP response elements from the Id2 promoter plus a SMAD4 DNA-binding motif; upon BMP pathway activation, the SMAD1/5/8-SMAD4 complex binds the BRE and drives reporter expression. Stable lentiviral integration enables generation of polyclonal reporter cell lines for analysis by fluorescence microscopy, flow cytometry, luminometry, or β-galactosidase assay. The system is applied to study BMP signaling in development, stem cell differentiation, and tissue homeostasis. Particles are purified by PEG precipitation and sucrose gradient centrifugation, supporting efficient transduction of difficult-to-transfect cells, including primary and cryopreserved cultures.

    About This Product

    This reporter lentivirus places a d2GFP, EGFP, Firefly Luc, GFP, mCherry, RFP, β-Galactosidase reporter gene under the control of tandem consensus response elements specific for the BMP Signaling Pathway transcription factor, coupled to a minimal TATA-box promoter and a proprietary upstream enhancer that maximizes signal-to-noise. The constitutively expressed selection marker (Blasticidin, Puromycin) and/or secondary reporter enables stable polyclonal cell line generation and flexible readout by fluorescence microscopy, flow cytometry, or luminometry.

    Stable integration via the lentiviral backbone ensures consistent, clonally representative reporter expression in dividing and post-mitotic target cells — including primary T cells, macrophages, organoids, and cryopreserved material — eliminating the variability inherent to transient transfection. The self-inactivating LTR design and third-generation packaging minimize insertional mutagenesis risk and ensure biosafety classification at BSL-2.

    How does this reporter lentivirus work?
    What reporter and selection marker options are available?
    How do I establish a stable reporter cell line?
    What positive controls are recommended to validate the reporter cell line?
    Can this reporter lentivirus be used in primary cells or non-adherent cells?

    Can't find the lentiviral construct you need, or want to adjust key design elements? Contact us to discuss custom LV design and optional add-ons.

    Common customization requests

    • Insert / payload: replace the gene/sequence, swap to a different isoform, add mutations, or optimize cloning features.
    • Expression design: change promoter (e.g., CMV/EF1α/PGK), add enhancers, or adjust regulatory elements.
    • Reporters: add/swap GFP/RFP/mCherry/luciferase (single or dual reporters where applicable).
    • Selection markers: add/swap puromycin/blasticidin/neomycin or fluorescent selection options.
    • Vector format: switch between OE, shRNA, CRISPR (sgRNA/Cas systems), or control vectors (where supported).

    Add-ons you can request

    • Control viruses: empty vector, non-targeting shRNA, reporter-only controls, or matched backbone controls.
    • Packaging / format: concentration options, aliquoting, or custom fill volume for screening workflows.
    • Documentation: construct map/sequence confirmation package (as available) and batch documentation.

    What to include in your request

    • Target cell type/model (cell line or primary cells) and intended readout (reporter, knockdown, OE, etc.)
    • Insert sequence (FASTA) or reference ID, plus any required tags/mutations
    • Promoter, reporter, and selection marker preferences
    • Desired scale and preferred format (aliquots / concentration requests)

    Email us at support@biohippo.com or use the Talk to a Scientist request form.

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