You Searched For: Electrophoresis Buffers

Final fill for mAbs Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO Cla...

Laboratory Quality Manager Your Role Your Challenge Our Services Portfolio Resources About Us Contact Us However many factors challenge this process. Workloads vary and demand can spike at any time leading to mistakes or delays in the lab if caugh...

Nucleic Acid decontamination with DNA Exitus Plus Technology DNA-Exitus Plus™ is a novel patented reagent for the removal of nucleic acid contamination from laboratory surfaces and equipment. Instructions for use: The optimal incubation time for s...

Avantor Flowmor™ Packaging System improves free-flowability of hygroscopic salts What are hygroscopic materials? Examples are calcium chloride sodium chloride potassium phosphate and variety of buffer salts. Flowmor is a unique packaging system wh...

Advancing next gen biologic manufacturing by implementing continuous downstream processing platform Webinar On demand Replay An integrated downstream process is needed to efficiently support ever increasing pipeline and demand of mAbs in clinical ...

Innovation supporting the Korean biopharmaceutical market Avantor Suwon South Korea Innovation & Technology Center The Avantor Suwon South Korea Innovation & Technology Center focuses on optimizing biopharmaceutical purification processes for cust...

J.T.Baker® BAKERBOND® PROchievA™ recombinant protein A chromatography columns and resins Enhance your separation power and increase product purity with the J.T.Baker® BAKERBOND® PROchievA™ protein A derived affinity chromatography resin. The BAKER...

Avantor® Biopharma Educational Material Learn all you need to know on biopharma its R&D and manufacturing processes and technologies advancing patient treatments and therapies. What Is Buffer Management Uncover the significance of effective buffer...

Aurora Manufacturing Facility Our 65000 sq. ft. manufacturing facility in Aurora OH USA includes a 12000 sq. ft. excipient processing center 3000 sq. ft. for repackaging 35000 sq. ft. warehouse 8000 sq. ft. office 8000 sq. ft. manufacturing area a...

Adopting novel technologies to improve monoclonal antibody processes Webinar On demand Replay Over last 20+ year there has been significant grown in monoclonal antibody drug pipeline as well as diversity of monoclonal antibody molecules. For examp...

Final fill for vaccines Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO...

Production The challenges of production include the scaling up of laboratory processes processing and production management personal and product safety. VWR are able to provide support in this environment from raw materials to hygiene control. We ...

Chemicals Chemicals Titration and Karl Fischer Titration – Advance your daily titration process and learn from experts Bettina Straub-Jubb Risk Assessment for Carcinogenic Substances in the Lab Dr Birgit Stöffler Ensuring Consumer Safety with Cert...

Advancing next gen biologic manufacturing by implementing continuous downstream processing platform Webinar On demand Replay An integrated downstream process is needed to efficiently support ever increasing pipeline and demand of mAbs in clinical ...

Upstream processing for mAbs Developing and manufacturing mAbs has moved away from a dependency on raw materials of animal origin. Our biochemical components and supplements are animal component-free to meet the needs of these applications. Produc...

Final fill for gene therapy Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an...