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Buy Sartorius Gene Therapy
Linkit® AX by Sartorius
Precise aliquoting solutions for cell and gene therapy
Uniform liquid distribution and full traceability
Optimise your aliquoting processes with the Linkit® AX solution, which offers fast filling performance, automation and standard-compliant batch protocols. Simplify liquid splitting and ensure full traceability according to FDA guidelines and EU requirements with this compact and user-friendly solution.
CellGenix® Growth Factors and Cytokines by Sartorius
Recombinant growth factors without animal products
Optimised cell culture for T cells and MSCs in gene therapy
Ensure consistent and reproducible results in cell and gene therapy research using these advanced raw and ancillary materials that are a staple in regenerative medicine.
Recombumin® Elite by Sartorius
ICHQ7 cGMP-compliant albumin for biotechnological applications
Increase consistency and safety for gene therapies and vaccines
Elevate your cell therapies, gene therapies, vaccines, and more with Recombumin® Elite - the secure, consistent, and regulatory-aligned solution for your medical advancements.
HEK Media by Sartorius
Serum-free cell culture media for HEK cells
Optimised for HEK293 cells and viral vector production, ISO 9001 certified
Experience our animal component-free HEK media suitable for various human cell lines, supporting stable growth and superior performance in suspension culture - backed by ISO 9001 QMS standards.
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Topic world Gene therapy
Genetic diseases once considered untreatable are now at the center of innovative therapeutic approaches. Research and development of gene therapies in biotech and pharma aim to directly correct or replace defective or missing genes to combat disease at the molecular level. This revolutionary approach promises not only to treat symptoms, but to eliminate the cause of the disease itself.
Topic world Gene therapy
Genetic diseases once considered untreatable are now at the center of innovative therapeutic approaches. Research and development of gene therapies in biotech and pharma aim to directly correct or replace defective or missing genes to combat disease at the molecular level. This revolutionary approach promises not only to treat symptoms, but to eliminate the cause of the disease itself.
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