Welcome to our pioneering Stem Cell, Genomic Sequencing, Cell Cure, and Gene Therapy laboratory, a hub of biomedical innovation leading the way in transforming healthcare. This facility is committed to leveraging the power of advanced genetic technologies like CRISPR/Cas-9, as well as cell-based treatments, to revolutionize the medical landscape.
Our spacious, state-of-the-art laboratory features a collection of cutting-edge clean rooms specifically designed to carry out intricate research on human stem cells, gene-modified cells, and for the development of curative cellular treatments. The labs are equipped with the latest instruments such as next-generation sequencing platforms for whole-genome sequencing, bioinformatics workstations for genomic data analysis, high-tech cell culture facilities, and advanced flow cytometers for detailed cell analysis.
Our CRISPR/Cas-9 suite is where we apply the transformative power of gene editing. This technology allows us to modify DNA sequences and gene function with extraordinary precision, enabling us to explore the genetic underpinnings of diseases and potentially devise therapies that could treat, or even cure, these conditions.
The genomic sequencing wing of our laboratory focuses on unraveling the complex code of life to understand and combat disease. Our high-throughput sequencing platforms enable us to rapidly and accurately sequence entire genomes, providing insights into the genetic basis of disease and facilitating the development of personalized therapies.
Our cell cure section concentrates on the development and application of innovative cellular treatments, including regenerative therapies and immune cell therapies like CAR-T cells. These cutting-edge therapies leverage the body’s own cells to repair, replace, or restore biological function lost due to disease or injury.
Our gene therapy unit focuses on devising novel therapies for genetic disorders. By utilizing viral and non-viral vectors to deliver therapeutic genes into cells, we’re able to correct or compensate for defective genes or induce the production of beneficial proteins.
Our commitment to safety and ethical practices is uncompromising. We adhere to stringent regulations and guidelines, ensuring the responsible and ethical use of these powerful technologies. Our facilities meet the highest biosafety and biosecurity standards.
The synergy among our multidisciplinary team of geneticists, molecular biologists, bioengineers, clinicians, and bioinformaticians fosters a dynamic environment that accelerates scientific discoveries and brings us closer to our primary goal – providing transformative therapies for patients globally.
We warmly welcome interested collaborators, students, and researchers to join us in our mission to push the boundaries of medicine through our groundbreaking work.