Media & reagents
GMP manufactured products designed for cell and gene therapy to support your transition from discovery through clinical and commercial manufacturing.
Gibco Cell Therapy Systems (CTS)Products designed to enable clinical and commercial cell and gene therapy manufacturing |
As you scale your cell and gene therapies beyond research, products designed to enable clinical and commercial manufacturing are essential to your success.
The Gibco CTS portfolio of cell and gene therapy products are GMP manufactured, safety tested and backed by regulatory documentation to support your transition from discovery through clinical and commercial manufacturing. Through our CTS solutions, we are committed to helping customers streamline therapeutic development, minimize risk, and ease the burden on their quality systems.
GMP manufactured products designed for cell and gene therapy to support your transition from discovery through clinical and commercial manufacturing.
Cell therapy instruments, supporting consumables and software products enable CGMP compliant, closed system manufacturing and allow for physical and digital integration.
Cost-effective, scalable solutions designed to transition your gene therapy workflow from discovery to commercial manufacturing.
Whether you're developing an induced pluripotent stem cell therapy, specialized immunotherapy, or a gene therapy, our Gibco CTS portfolio offers cell-type and viral vector specific applications that can be leveraged to advance your research to the clinic and beyond.
Specialized Cell Therapy Systems products to isolate, activate, expand, and genetically modify T cells, dendritic cells, or other immune cell types.
Explore cell therapy systems products for expansion, processing, and gene editing of human natural killer (hNK) cells for cell therapy development.
Learn more about our solutions across the pluripotent stem cell workflow, from reprogramming to culture.
Specialized cell therapy products for stem cell– and tissue-derived neural cell cultures.
We offer complete, optimized systems for scalable, cost-effective adeno-associated virus (AAV) and lentivirus (LV) vector production.
Providing quality for our customers drives everything we do. In addition to our comprehensive CTS portfolio of products, we offer regulatory documentation to support your transition from research through to commercialization. Experienced cell and gene therapy professionals, technical support teams, and highly specialized scientific teams are available to answer your questions, provide detailed product and protocol consultation, as well as customization services.
The Gibco CTS AAV-MAX Helper Free AAV Production System enables a smooth transition from discovery through manufacturing, offering one optimized, scalable platform with CGMP manufactured reagent options.
Learn more
Gibco CTS NK-Xpander Medium is designed to proliferate a high yield of functional human NK cells to address the needs of translational and clinical cell therapy researchers with or without the use of feeder cells.
Learn more
The CTS DynaCellect Magnetic Separation System is a closed, automated isolation, activation, and bead removal system for cell therapy development and manufacturing.
Learn more
We are committed to delivering products that serve the research needs of our customers, while striving to develop them in a way that minimizes our use of natural resources and our impact on the environment.
Packaging must protect the product inside—but that doesn’t have to mean sacrificing sustainability. GlutaMAX-I Media Supplement ships at ambient temperature. By “going ambient” for the GlutaMAX Supplement, we help divert an annual total of nearly 2,000 kg (2,700 ft3) of EPS from landfills and incinerators, and reduce the total carbon footprint by over 100 tons annually.
For Research Use or Manufacturing of Cell, Gene, or Tissue- Based Products. CAUTION: Not intended for direct administration into humans or animals.
* CTS products are designed to meet USP <1043>, ancillary material responsibilities for cell, gene, and tissue-engineered products, under a robust Quality Management System certified to ISO 9001 or 13485. All aspects of USP <1043> are the responsibility of the end user to assess. We are dedicated to supporting our customers clinical translation. For regulatory documentation support please contact us.