A groundbreaking innovative method (patent pending) for generating
LT-HSC through an ex vivo chemical signalling process.
This process also enhances cellular quiescence homeostasis in a
hematopoietic stem cell culture, facilitating the efficient delivery for gene reprogramming and gene editing for common diseases.

Our technique produces LT-HSC from the peripheral blood of patients, allowing for the generation of cells that can self-renew indefinitely for months or even years.

This process takes less than 24 hours and can be implemented in hospitals at minimal expense, making advanced therapies accessible to more patients.

Our LT-HSC generation is suitable even for elderly patients, including those over 70, expanding the range of individuals who can benefit from these therapies.



LT-HSC has never been successfully generated ex vivo by anyone else, positioning us at the forefront of hematopoietic stem cell research and therapy. Some of which will likely include the unlimited potential to augment CRISPR/cas 9 sgRNA guided in combination of AAV transduced template of HDR cDNA.
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