Ensuring effective delivery of your genes of interest (GOI) is the critical mission of virus packaging. GENEWIZ Genomics Services from Azenta Life Sciences brings over 20 years of genomics experience to your research project, providing both the Ph.D. consultation and wet lab expertise to give you fast and reliable delivery of viral plasmids and particles. Our project managers customize and scale your projects to meet the most rigorous technical requirements with the utmost quality.
Learn how partnering with GENEWIZ can help your AAV, lentivirus, or baculovirus research succeed in making the world a healthier place for people everywhere.
With low immunogenicity limiting the risk of integration into the host genome, adeno-associated viruses (AAVs) have emerged as promising vehicles to deliver both cell and gene therapies. These viruses, however do pose major challenges in both synthesis and packaging to obtain high titer and efficacy.
Learn how our proprietary AAV solutions overcome technical challenges to deliver reliable cell transfection and confident research results.
Lentiviral vectors are research tools used to introduce gene products into in vitro systems, animal models, or human patients via gene therapy. Lentiviruses have a broad range of applications and are commonly used in clinical gene therapy as well as in CAR-T cell engineering.
Learn how our gene-to-lentivirus solutions, combined with our sample management services, can help you streamline your laboratory operations and accelerate your research.
Baculovirus has been widely used to produce recombinant proteins on both insect and mammalian cells. The virus is an ideal tool for gene delivery and gene therapy due to its large gene capacity, which allows expression of proteins with large molecular weight, high safety through strict species specificity, high expression efficiency, and ease of amplification.
Explore our expanded gene-to-baculovirus synthesis and expression offering to find your preferred solution.