Join us to celebrate the achievements of the 60 impactful analytical scientists featured in the 2024 Power List.
09/16/2016 | Rich Whitworth
Rich proposes a toast to friendship and mentorship within the analytical science community
09/06/2016 | Sponsored by Malvern Panalytical
10 reasons for polymer characterization scientists. Gel-permeation chromatography (GPC) is an essential tool for the characterization of polymers. It allows polymer scientists to tailor a polymer’s properties to its end use requirements by controlling its molecular properties, since the two are inextricably linked.
08/16/2016 | Kevin Schug, Luigi Mondello, Nicholas Snow
Three experts share their views on gas chromatography-vacuum ultraviolet (VUV) detection
08/15/2016 | Rich Whitworth, Joanna Cummings
Whether testing tomatoes or assessing wine spoilage, analytical science is key to consumers.
08/15/2016
We speak with scientists using analytical techniques to solve some of the art world's mysteries
08/15/2016 | Rich Whitworth, Marcus Lippold
Products, partnerships, investments - what’s going on in the analytical science business world.
08/12/2016 | Kyle D’Silva
Hear from Kyle D’Silva as he discusses new developments in GC-MS technology for Extractables and Leachables testing
08/03/2016 | Sponsored by Malvern Panalytical
This whitepaper reviews the methods available for measuring the key characteristics of polymers focusing on the benefits and value of gel permeation / size exclusion chromatography (GPC/SEC). Much of the paper talks exclusively about polymers, however many of the principles discussed are equally applicable to proteins or protein conjugate materials.
Traditionally in GPC, the sample dissolution solvent and the mobile phase are one and the same. However, a closer look at the demands of sample solvent and mobile phase suggests that this should not always be the case.
The complementarities of two techniques, dynamic light scattering (DLS) and static light scattering detector coupled with a size exclusion chromatography system (SEC-LS), are illustrated by studying a number of samples where a thermally denatured and aggregated protein sample were dosed at different levels into a non-denatured protein sample.
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