This site uses cookies to provide you with a more responsive and personalized service. By using this site you agree to the Privacy Policy and Terms of Use. Please read our cookie policy for more information on the use of cookies on this website.
Gain operational efficiency, simplified workflows, and control over your lab. Tailor our comprehensive cold-chain sample management, lab automation, and multiomic solutions to support your sample lifecycle needs, from collection to end use.
Improve sample tracking, ensure sample integrity and drive process efficiency with Azenta Sample Storage Tubes. Explore the range, and select the best tube for your workflow.
Fit automation into any space from lab to clinic and keep samples and staff safe without exposing innocent samples to transient warming, while ensuring accurate chain of custody records.
Life science organizations must collect and manage large numbers of research samples to bring a new therapeutic or diagnostic to market. This is a complex process.
Comprehensive genomics sequencing, synthesis and multiomics solutions for research, discovery and clinical phase customers.
The cryo monitoring portal is built to help you track the status of all your cryo freezers and equipment in real-time from anywhere.
Azenta Life Sciences' world class service team is committed to ensuring you meet your business objectives by providing a flexible portfolio of service products designed to optimize up-time and productivity.
Azenta Life Sciences has established, documented, implemented and currently maintains a quality management system that fulfills the needs of customers.
We are Azenta Life Sciences. We provide unrivaled sample exploration and management solutions to help our customers accelerate discovery, development and delivery.
Bridging the Gap is a new webinar series focused on cell and gene therapy. Read the recap of the first session featuring Dr. Grupp, a leader in CAR T-cell therapy.
Generating recombinant adeno-associated virus (AAV) with high-fidelity DNA can be challenging. Learn the best practices for working with AAV vectors.
We discuss how lentiviruses have been engineered to deliver transgenes safely and how researchers today generate lentiviral preparations.
Artificial DNA synthesis, a fundamental tool of synthetic biology, enables scientists to create DNA molecules of virtually any sequence without a template.
Diagnosed with cancer at age five, Emily Whitehead was the first child to receive CAR T-cell therapy in 2011. Now, her family is helping other children.
Clinical trials for cell and gene therapies involve many cold chain complexities. Learn how to better manage logistics for samples and materials.
Manufacturing and distribution of cell and gene therapies relies on stable low temperatures. Explore ways to increase rigor when storing CGT materials.
For gene therapy vectors like AAV, genomic features can interfere with traditional QC methods. Learn how recent innovations overcome these challenges.
Learn about the challenges of preparing and validating plasmid DNA for AAV vectors containing ITRs and an optimized approach to these processes.