CRISPR and Genome Editing – Multimedia

It is expected that within four to five years, biologics will comprise over half of the 100 top selling drugs on the market. However, the high cost and complexity of biotherapeutic development, as well as a dynamic regulatory landscape, still poses challenges to drug developers.

Electroporation has transformed the way in which scientists work, allowing the delivery of genetic material, proteins and drugs. Download this guide to discover tips on preparing your samples and selecting your parameters.

This eBook highlights ways that you can level up your vaccine research with selected bioreactor tools to fit your vaccine development workflow.

This poster highlights several methods by which the downstream purification of viral vectors can be improved using chromatography methods to analyse and purify multiple AAV serotypes.

The gene editing technology CRISPR is one of the most talked about scientific discoveries of recent years. Before it was discovered, researchers were limited to far more complex, expensive and time-consuming gene editing technologies.

Hear from three Simple Western users on why they use our next-generation, automated, western blot systems for cell and gene therapy workflows. Simple Western is a gel-free, blot-free, hands-free capillary western blot analysis.

In this informative video, you will discover the latest technologies and workflows used in the field of cell and gene therapy.

This infographic features solutions that can help to optimize this journey.

Adeno-associated viruses (AAVs) are considered one of the most effective and safe ways to deliver therapeutic genes for the treatment of a wide range of genetic conditions.

Whether your key vector strategy is based on adenoviruses (AV), adeno-associated viruses (AAV) or lentiviruses (LV), the development of these genetic analysis tools is enabling researchers to develop safer gene therapies – with greater speed.