At the heart of gene therapy is the process of reprogramming cells, using genetic instructions delivered by vehicles called viral vectors ... any gap in vector production could bring costly ...

Viral vectors can be used to deliver antigenic proteins or genes encoding them, eliciting protective immune responses against infectious diseases or cancer. Notable examples include the development of ...

Many viral vectors have ... As these vectors progress to the next level of phase I and phase II clinical studies, it is important to establish vector purification schemes that are both amenable ...

For all request of viral vectors, please visit the Gene Vector Core Website or send an email to [email protected] ... we will privately contact the owners and ask if we can provide other customers ...

The process of creating adenoviral vectors involves inserting the transgene into a small shuttle plasmid so that the transgene cassette can be excised with two restriction enzymes with almost unique ...

Adeno-associated viral (AAV) vectors in particular have high transduction rates and reduced toxicity concerns compared to other viral vectors. However, these delivery vehicles present some application ...

adenoviruses and other viral vectors are used in gene and cell treatments to transfer genes. As infection with the vector is not harmful and AAV cannot reproduce on its own, AAV-mediated gene ...