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Advancing AAV purification strategies
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Polishing is more than a final cleanup step in AAV purification. In this article, explore how capture conditions, AEX buffer chemistry, load conditioning, and elution strategy can work together to help improve full capsid enrichment and support scalable, reproducible manufacturing. Review practical considerations for translating optimized workflows from development to GMP scale using Thermo Scientific™ POROS™ resins and prepacked column formats, helping inform more confident AAV process design decisions. Read the article.
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By BioPhorum
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Here's a holistic approach to developing a comprehensive particulate control strategy for cell therapies, focusing on particle characterization, detection, and manufacturing controls.
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Optimizing Cell Culture Media Selection For High-Titer AAV
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Application Note | By Leah Hirsh, Katharyne Bostin, Cameron Wilcox, et al., Lonza
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To maximize the results of viral titer and full capsids, it's necessary to undertake systematic process development and optimization of AAV production. The choice of cell culture medium is foundational.
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A Simple, Effective Method For Cell Growth Media Preparation
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Poster | By Stijn De Backer, Mustapha Hohoud, Valeria Mastrullo, and Sabrina Cencig, Cytiva
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Explore how powder media and sterile fluid handling can reduce contamination risk and improve efficiency in viral vector production, especially for HEK293-based AAV workflows.
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Webinar: Annex 1 in Practice: Turning CCS Into Cleanroom Design
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How can facility design help prevent contamination before it threatens product quality? This AES webinar explores how EU GMP Annex 1 and a proactive Contamination Control Strategy (CCS) can shape cleanroom design, airflow, barrier technology, personnel and material flow, and aseptic processes. Learn how embedding contamination control from concept through operation can reduce regulatory risk and support inspection-ready manufacturing facilities. Click here to learn more.
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| Connect With Cell & Gene: |
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