GORE AME-Clamps enable convenient flow metering or precise flow closure within tubing systems for bioprocessing operations. These lightweight single-use clamps are easy to install over tubing, and the locking screw is fully adjustable using just one hand.

GORE Protein Capture Devices with Protein A are intended for the affinity purification of monoclonal antibodies and other proteins containing an Fc region derived from clarified cell culture harvests in process development to initial GMP clinical applications.

Discover how rapid cycle Protein A membrane chromatography can boost your antibody purification process productivity by trying the new GORE? Productivity Calculator.

A few quick inputs and you will see the difference high flow, high binding membranes can make. Please fill out form below to request the document.

A discussion on how new updates to quality standards encourage medical device manufacturers to expect more from their upstream component suppliers.

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This application note provides data demonstrating high productivity, extended cycling durability performance of membrane-based GORE Protein Capture Devices with Protein A across two rapid Clean-in-Place methods bracketing caustic contact time and concentration. These data were then combined with results from a manufacturing-scale demonstration to extrapolate protein capture capabilities at a 2000 L batch bioreactor size across CIP methods.

Custom-configured GORE Molded Assemblies with the GORE Aseptic Sampling Valve offer bioprocess operators a way to streamline the collection of multiple aseptic samples from stainless steel vessels.

An intensified and fully single use downstream operation was demonstrated to process a monoclonal antibody cell culture harvest at a manufacturing scale.  The results of the study were combined with previously published data to show the potential for high productivity affinity capture sufficient up to 10 g/L titers at the 2000 L scale.

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This application note demonstrates the scalability across multiple GORE Protein Capture Device sizes through dynamic binding capacity, CHO cell harvest, and purification experiments as demonstrated with a partially purified monoclonal antibody.

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