TransMega™ Lentiviral & Adenoviral Transduction Reagent (XS-1225-HM1)

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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.

TransMega™ Lentiviral & Adenoviral Transduction Reagent is an innovative chemical formulation designed to enhance lentiviral and adenoviral transduction efficiency in activated T cells. When used in combination with specific proteins, it significantly boosts gene delivery. It promotes T cell expansion while maintaining higher cell survival rates. Additionally, this product is safe for T cells and eliminates the need to replace the media after infection.

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Specifications

  • Applications
  • T cell transduction; T cell expansion; Process development and scale-up; Cell and gene therapy research
  • Storage
  • Store at -20° C
  • Shelf Life
  • 24 months
  • Features
  • User-Friendly: Direct addition to culture media for streamlined workflow.
    Biocompatible: Safe for T cells; no need to replace media after infection.
    Universal: Effective with all packaged lentivirus types.
    Expansion-Compatible: Preserves T-cell proliferation and viability.
    Adaptable: Enhances transduction efficiency across different T-cell activation methods.
  • Protocol
  • Protocol 1
    Step 1: Thaw cells (Pan-T cells or PBMCs)
    Step 2: Activate cells in 1x10e6/ml using anti-CD3 antibody, magnetic beads, or transduction enhancement reagent.
    Step 3:
    1. Coat the plate with extracellular matrix protein and incubate for 2 hours at room temperature.
    2. Block the coated plate with an appropriate volume of sterile 2% BSA in PBS for 30 minutes, then remove the blocking buffer and rinse with PBS to keep the wells moist.
    3. Remove the activation reagent and prepare T cells at 1 × 10⁶/mL.
    4. Add the appropriate MOI of lentivirus or retrovirus and this product (1000×) to the T cells.
    5. Transfer T cells with virus and this product to coated wells.
    Step 4: Analyze transduction efficiency by flow cytometry.
    (Total cycle time: approximately 7 days)

    Protocol 2
    Step 1: Thaw and activate Pan-T cells or PBMCs at 1.5 × 10⁶/mL using anti-CD3 antibody, magnetic beads, or transduction enhancement reagent.
    Step 2:
    1. Coat the plate with extracellular matrix protein and incubate for 2 hours at room temperature.
    2. Block the coated plate by adding an appropriate volume of sterile 2% BSA in PBS for 30 minutes. Remove the blocking buffer and rinse with PBS to keep the wells moist.
    3. Add the appropriate MOI of lentivirus (or retrovirus) and this product (1000×) to the T cell mixture (0.5-1 × 10⁶/mL) with activation reagent.
    4. Transfer the T cell, virus, and reagent mixture to the coated wells.
    Step 3: Centrifuge to change the medium.
    Step 4: Analyze transduction efficiency by flow cytometry.
    (Total cycle time: approximately 6 days)
  • Shelf Life
  • 24 months

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For research use only. Not intended for any clinical use. No products from Creative Biolabs may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative Biolabs.

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