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Preparative/Process Chromatography

Business & Education Sample Preparation

Protein measurements with the Zetasizer µV

| Sponsored by Malvern Panalytical

This application note describes a selection of measurements made on a GE AKTA basic system.

Techniques & Tools Sample Preparation

Performance of Polymer Solutions for Enhanced Oil Recovery

| Sponsored by Malvern Panalytical

In this article we take an introductory look at work carried out by TU Clausthal to develop an improved understanding of the mechanisms of enhanced oil recovery (EOR) by polymer flooding, and the relevance of fluid rheology. Example data illustrates the insight that rheology provides and its application in optimizing fluid performance.

Business & Education Sample Preparation

Why should I upgrade to multi-detection GPC?

| 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.

Business & Education Sensors

Case studies: Ink formulation's analytical strategies

| Sponsored by Malvern Panalytical

This white paper offers practical guidance on using a range of analytical techniques, including rheology, particle size and zeta potential measurement to assist in the formulation of Inkjet inks.

Techniques & Tools Sample Preparation

Solvent Enhanced Light Scattering of Fluoro-Polyester

| Sponsored by Malvern Panalytical

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.

Business & Education Sample Preparation

Detection and quantification of large protein aggregates

| Sponsored by Malvern Panalytical

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.

Business & Education Sample Preparation

Intrinsic viscosity measurements on sRAGE protein

| Sponsored by Malvern Panalytical

In this application note, intrinsic viscosity measurements were performed on the sRAGE protein to establish whether the detector was able to detect and characterize the conformational change induced by the presence of calcium. Light scattering molecular weight measurements were also performed. Data are also presented showing that the conformation of sRAGE changes in the presence and absence of calcium.

Techniques & Tools Sample Preparation

The Benefits of Multi-Detector SEC for Protein Analysis'

| Sponsored by Malvern Panalytical

This article explores how multiple detectors, particularly light scattering detectors, may be used for size-exclusion chromatography (SEC) in protein analysis. Using a light scattering detector as part of a multi-detector Size Exclusion Chromatography system provides the accurate molecular weight (MW) data needed to assess the activity, safety and clinical efficacy of therapeutic proteins.

Techniques & Tools Sample Preparation

Optimizing Food Additive Choice: Exploring the Value of Recent Advances in SEC Technology

| Sponsored by Malvern Panalytical

The latest advances in the widely used technique of size exclusion chromatography (SEC) break new ground in terms of accuracy and sensitivity. This article assesses the information provided by multi-detector SEC and the potential benefits of recent innovations for polymeric food additive characterization.

Techniques & Tools Sample Preparation

Protein Applications for Advanced Multi-Detector Size-Exclusion Chromatography

| Sponsored by Malvern Panalytical

In this application note, a mixture of four proteins was characterized in a single SEC measurement using multiple detectors. The generally consistent response to the RI to proteins makes it a useful total protein concentration detector, while the UV detector can be used to measure the concentration of individual proteins when the extinction coefficient is known. This is particularly useful for proteins that elute in the solvent peak making RI measurements unreliable. Finally, light scattering measurements allow each peak to be identified by its molecular weight.

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