Solution
Intracellular delivery nanobiochip
The Unique product line leverages patented technology to precisely control interactions between nanoscale probe arrays and cells, delivering genetic material directly into cells. This enables gene modification or editing without damaging the cells, providing a powerful new toolkit for cellular engineering. The technology significantly enhances transfection efficiency, particularly for hard-to-transfect cells, and holds broad potential for applications in cell therapies, including CAR-T and iPSC manufacturing.
Solution list
Efficient delivery of genetic material into cells enables high transfection across a variety of mammalian cell types, including hard-to-transfect cells. In certain cell types, transfection efficiency is increased up to tenfold compared to liposome-based methods.
Overcoming challenges such as low cellular uptake and high off-target editing, our technology enables the non-disruptive delivery of Cas9 protein and sgRNA, supporting gene knockout, base editing, and epigenetic regulation. It provides a highly efficient, precise, and stable solution for demanding gene editing applications.
Addressing the low efficiency and high toxicity of traditional transfection methods, this technology is designed for efficient and precise siRNA delivery and gene knockout, providing a one-stop gene silencing solution for research and drug development.
Significantly enhances the intracellular delivery efficiency of viral particles, including lentivirus, AAV, and adenovirus, reducing viral usage by over 50% while maintaining normal transduction efficiency at low viral doses, thereby lowering overall viral costs.