Bioprocessing Application Notes & Case Studies
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Fast And Scalable Fc Quantitation In Supernatants
3/24/2025
In biopharmaceutical development, the Fc PAIA Titer assay offers a fast, cost-effective, and automatable solution for high-throughput Fc quantification to enhance efficiency, support research, and accelerate production advancements.
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Evaluating Compound Toxicity Effects On Healthy Intestinal Organoids
3/24/2025
3D organoids enhance drug toxicity prediction and are crucial for anti-cancer drug development. Examine a method using 3D mouse intestinal organoids that aims to provide vital data on intestinal toxicity.
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Cell Culture Automation Of The 3D Cancer Spheroid Assay
3/24/2025
Discover how automated 3D cell culture methods enhance efficiency and consistency in high-throughput drug screening to accelerate the discovery of new anti-cancer therapies.
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Studying The Spatial Architecture Of Glioblastoma
3/24/2025
Explore how intra-tumor heterogeneity (ITH) impacts cancer progression and therapy resistance with advanced imaging platforms and custom antibody panels to reveal the spatial architecture of glioblastoma (GBM).
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Multiplex Imaging
3/24/2025
Explore recombinant antibody reagents that support the imaging of key targets within the TME and offer flexible solutions across various platforms to improve patient outcomes.
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Enhanced Validation Data Anti-EGFRvIII Recombinant Antibody
3/24/2025
Select the right antibody clone by exploring enhanced validation data for top recombinant antibody clones that offer comprehensive specificity and sensitivity insights tailored to your project's unique requirements.
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Catalent's Journey Of Continuous Improvement For CSV Excellence
3/19/2025
Discover how organizations like Catalent must continuously reassess validation processes and digital tools to ensure compliance, enhance efficiency, and support global scalability amidst evolving regulatory expectations.
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MilliporeSigma's 97-Day Implementation Success Story
3/19/2025
Discover how MilliporeSigma transformed validation processes with a digital validation system to achieve efficiency and compliance in just 97 days as well as learn key takeaways from their swift transition to digital validation.
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Single-Use Assembly Capabilities To Keep Pace With Biopharma Dynamics
3/17/2025
Discover how a vendor-independent partner assists global life science companies and CDMOs with innovative single-use technologies to mitigate risks and ensure uninterrupted manufacturing.
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Assessment Of Compound Toxicity Effects With High-Content Imaging
3/17/2025
3D cellular models and bioprinting enhance drug safety predictions and offer precise spatial control. Explore an automated method for generating liver models to improve reproducibility and reliability in toxicity testing.