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Resources

Explore our media section to discover insightful videos, informative podcasts, and engaging articles showcasing the innovative applications and advancements in cell testing technology.

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Game changing RNA delivery platform for next generation therapy : FlashRNA® (ESGCT 2023)
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Game changing RNA delivery platform for next generation therapy : FlashRNA® (ESGCT 2023)
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Gene editing on primary & stem cells using LentiFlash (FlashRNA®) RNA delivery approach (ASGCT 2022)
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NK cells engineering using advanced Lentiviral Vectors quality and design (EBMT 2023)
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GMP platform for lentiviral vector production with 9000 batches produced (Advanced Therapies 2023)
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Lentivirus Manufacturing : successful & reproducible continuum process from research batches to clinical application (ISCT 2023)
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Next Generation Therapy : RNA delivery by LentiFlash (FlashRNA®) for an efficient CRISPR/Cas9-mediated gene knockout in Human iPS (EBMT 2023)
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Efficient & safe delivery of multiple mRNA using non-integrative bacteriophage-chimeric retrovirus-like particles for in vivo application (ASGCT 2022)
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All-in-one delivery using LentiFlash (FlashRNA®) for clinical application (ESGCT 2019)
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All-in-one Delivery Using LentiFlash® technology, a MS2-chimeric RNA Delivery Tool Designed for Clinical Applications (ASGCT 2019)
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Primary cells and in vivo immunomodulation using LentiFlash®, a chimeric RNA delivery technology designed for clinical applications
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All-in-one delivery of gene-editing system into primary cells and in vivo using LentiFlash® (FlashRNA®), a new tool fo knock-in & knock-out applications

FAQ

Explore our media section to discover insightful videos, informative podcasts, and engaging articles showcasing the innovative applications and advancements in cell testing technology.

How do Flash BioSolutions lentiviral vectors differ to those from other providers?

Flash BioSolutions has developed a proprietary purification & concentration process for lentiviral vectors production. Purification levels are tailored to your application.

Flash BioSolutions generates high titer and highly pure lentiviral particles that guarantee cell viability and phenotype. Our technical experts are dedicated to the success of your project, from cassette design to transduction protocols.

What are the differences between AAV and Lentiviral vectors?

Each method has both advantages and drawbacks for specific applications, depending on its technical characteristics. For example, the use of AAVs for the transfer of genetic material is limited by the length of the sequence of interest and by the pseudotype; non-viral methods can be problematic for the study of gene expression in primary cells because of cell toxicity and/or lower efficiency.

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