Monolithic columns combined with exceptional affinity ligands present an unmatched solution for affinity purification of enormous biomolecules.

The content material of our website is often available in English and partly in other languages. Pick your chosen language and We are going to demonstrate the information in that language, if out there.

Be part of our webinar to discover what will make monoliths perfect for the problems of purifying massive biomolecules.

This website page doesn't exist in the chosen language. Your preference was saved and you may be notified after a web page could be considered within your language.

Procedure growth and production can have to manage a number of resins ranging from little to huge particles, from narrow to huge distribution of particle size and from comfortable to rigid, maybe even brittle particles.

Huge array of procedures and move route configurations available to structure your own private multi-stage program.

This chromatographic process relies on the potential with the bonded Energetic substances to sort steady, specific, and reversible complexes thanks to their biological recognition of specific precise sample elements. The formation of these complexes entails the participation of common molecular forces like the Van der Waals conversation, electrostatic conversation, dipole-dipole conversation, hydrophobic conversation, as well as hydrogen bond.

A connected process is a lot more compact and less difficult to manage. In this particular webinar, we give an overview on ways to configure the Resolute® BioSC.

Immobilized Chiral Columns: The chiral selector is covalently bonded for the stationary stage, making sure security and efficiency. Immobilized chiral columns are particularly valuable for extensive-time get more info period use and sturdy separations.

Be sure to verify you click here want to to obtain advertising and promotional email messages about Thermo Fisher Scientific products and services.

HPLC columns consist of a stationary stage bonded to the aid materials, normally porous silica particles, to supply a significant surface area location. The stationary period presents The premise for separating sample factors.

Tailing peaks surface asymmetrical and also have a distorted condition. This can be brought on by degradation in the column’s stationary phase, but can be the result of other non-column connected things.

The cellular phase carries a liquid sample from the column into the detector, and compounds or analytes separate as a result of different levels of conversation Together with the stationary section.

Our columns meet large style and design requirements, thus making sure performance and scalability. DAC technologies enables reproducibility and robustness as time passes.