Gene transfer | Cytiva

Efficient gene transfer

When preparing genetically engineered cells, including T cells, efficiency is an important factor. Whether you are starting from scratch or moving to the next phase, an automated and closed process that does not require additional chemicals offers a clear advantage.

General cell processing workflow with gene transfer highlighted

Closed and automated viral transduction

Transduction using viral vectors is a popular method for generating genetically engineered cells such as CAR T. Combine SpinOculation C-Pro protocol with the Sepax C-Pro instrument and a single-use kit for a rapid and functionally closed T cell transduction process that preserves cell viability and virus stability.

Generic Sepax C-Pro + software + kit illustration

Vector manufacturing

Obtain the quantity and quality of vectors needed for your gene transfer work. Our portfolio offers technologies for making your own, plus process development and contract manufacturing services. Supports cell therapy and gene therapy viral vectors including adeno-associated virus and lentivirus vector. Photo credit: CCRM

VECTOR PD, CMO, AND EQUIPMENT

Contract Manufacturing for cell and gene therapy

Manage risk and protect cell quality with automated and functionally closed systems. Use with rigorously tested density gradient media or magnetic beads.

Maximize cell density and maintain quality by combining high-quality media and reagents with automated and functionally closed systems.

Simplify workflows by automatically sequencing multiple steps. Functionally closed processing helps you manage contamination risk.

Preserve cell viability and function with automated dry freezers and thawers. Connect units across sites and monitor remotely using platform software.