AGC Biologics signed a licensing agreement to use Asimov’s lentiviral packaging system, enabling production from a single-plasmid transfection.

First commercially available cell culture solution for HEK293 cells and perfusion -– optimized for high cell density (HCD), intensified processes and perfusion cultures Additional capabilities for ...

Article subjects are automatically applied from the ACS Subject Taxonomy and describe the scientific concepts and themes of the article. The advent of mRNA-based therapeutics has transformed ...

This research investigates how to optimize mRNA transfection in human T-cells utilizing the jetMESSENGER ® transfection reagent. By using advanced bioanalytical instruments like the Incucyte ® ...

Transfection is a crucial non-viral technique for introducing DNA or RNA into cells, yet achieving high efficiency and consistency can be challenging, particularly with difficult cell types.

School of Natural Sciences, University of Kent, Canterbury, United Kingdom Delivery of DNA into nucleated eukaryotic cells is known as transfection and has been essential in establishing technologies ...

Gene Therapy Department, Research Center for Translational Medicine, Sirius University of Science and Technology, Sirius, Russia Adeno-associated virus (AAV)-based gene therapy has become one of the ...

The useful studies described here are broadly applicable to all antibody discovery subfields, even though they are not a significant improvement over published methods. The findings are incomplete ...

Cell and gene therapy (CGT) biotechnology companies Opencell Technologies and Adva Biotechnology have announced a strategic partnership that integrates platforms from both companies in support of an ...