Authors
Creative Bioarray
Summary
Gene therapy is a technique in which a functioning gene is inserted into a human cell to correct a genetic error or to introduce a new function to the cell. Genetic material is administered to modify or manipulate the expression of a gene product, either RNA or protein, or to alter the biological characteristics of living cells for therapeutic use.
Introduction
Gene therapy has the potential to provide long-term therapeutic efficacy, but their development is both risky and cost-intensive. A better understanding of the specific structural properties of vector proteins that influence clinical delivery and outcomes is critical to advancing both individual candidates and the platforms on which they are based. Strategic application of advanced analytical techniques can help improve the selection of candidates and guide development decisions, leading to more safer and more efficacious gene therapies successfully completing development and entering the market. Creative Bioarray is here to help you get safe and effective treatments for those who need them. From development to manufacturing and QC, our platform provides automation and scalability for rapid and accurate characterization with low-volume sample analysis to help preserve your precious samples. Whether you’re developing viral vector-based therapy, such as adeno-associated virus (AAV) or lentivirus (lenti) product, or applying gene editing technologies such as CRISPR/cas9, you’ll benefit from the deep knowledge and experience of our expert team.
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