mRNA-based therapeutics have demonstrated immense potential to revolutionize disease treatment. However, the broad application of genetic medicines remains limited by the challenges of current delivery technologies. At Nanoportal Biotech, our mission is to leverage natural biological mechanisms to develop the next generation of gene delivery systems. We have successfully invented the world's first coacervate-based nucleic acid delivery platform based on mammalian endogenous protein, offering a novel solution for efficient gene delivery.
ABOUT USEfficient Transfection of Hard-to-Transfect Cells
Efficient Transfection of Primary Cells
Efficient Transfection of Mouse Primary Immunocytes
For gene editing in Hard-to-Transfect Cell Lines
For gene knockout in Primary Cells and Hard-to-Transfect Cell Lines
For gene knockout in mouse primary immune cells
ProteanFect breaks through the problem of transfection of primary T cells in mice, and West Lake University launches the world's first ...
2022.11.23ProteanFect breaks through the problem of transfection of primary T cells in mice, and West Lake University launches the world's first ...
2022.11.23ProteanFect breaks through the problem of transfection of primary T cells in mice, and West Lake University launches the world's first ...
2022.11.23