GMP Ready GMP Plasmids

GMP-ReadyTM/GMP Plasmids

GMP-Ready and full GMP plasmid are premanufactured, fully documented and ready-to-use. GMP production and full QC release of plasmid DNA usually needs several months. These in stock GMP-Ready and GMP plasmids will save your time and accelerate your gene and cell therapies.

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pHelper-Kan GMP-ReadyTM AAV Helper Plasmids

Vigene Biosciences is a world leader in adeno-associated virus (AAV) production. pHelper-Kan provides adenoviral helper function genes, E2A, E4, VA, and is used in AAV viral vector production utilizing the triple plasmid transfection method. To save your time and accelerate your gene and cell therapies into the clinic, Vigene pre-manufactures pHelper-Kan GMP-Ready plasmids to accelerate the GMP AAV manufacturing. The GMP-Ready plasmids are produced and released according to batch production records .
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Need Custom Plasmid Production for Your Viral Vector Manufacturing?

Vigene can help to produce Rep-Cap plasmid and your transfer vector containing the therapeutic gene. We have the full range of plasmid manufacturing services for applications ranging from preclinical research studies all the way up to clinical trials and commercial manufacturing.

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Need Custom cGMP AAV Packaging?

Vigene is a world leader in AAV manufacturing, with a 17-year GMP production track record. We have the capability and capacity to manufacture AAV viral vectors for applications ranging from preclinical to clinical, commercial settings.

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Need Custom cGMP Lentivirus Packaging?

Vigene has expertise in GMP production of lentiviral vectors in HEK293 and 293T producer cell lines (adherent or suspension cells).

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  1. pHelper-Kan GMP-Ready Helper Plasmid for AAV GMP Manufacturing
    GR-PHELPER-KAN
    Plasmid DNA
    Kanamycin
    11.6 kb

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GMP-Ready and full GMP plasmid are premanufactured, fully documented and ready-to-use. GMP production and full QC release of plasmid DNA usually needs several months. These in stock GMP-Ready and GMP plasmids will save your time and accelerate your gene and cell therapies.