The Adeno-Associated Virus (AAV) is the most promising candidate for virus-based gene therapy as it:
- Infects both dividing and non-dividing cells.
- Has low immunogenicity and pathogenicity.
- Can target a broad range of specific tissue types.
- Provides long-term expression in non-dividing cells.
Our complete library of premade AAV vectors and pre-packaged AAV particles for human, mouse, and rat genes come with a wide selection of promoters and reporters for every need. For gene knockdowns, access our AAV-siRNA vectors and viruses as well as our AAV-miRNA over-expression and inhibition tools.
더 많은 정보 보기 AAV Library
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