Pre-packed columns, cartridges, and guard columns for separation of biomolecules and organic/inorganic analytes; includes normal/reversed phase HPLC, UHPLC, LC-MS, HILIC, mixed-mode, ion exchange, ligand exchange, and affinity column formats.
Les produits de certains de nos fournisseurs ne s'affichent pas dans les résultats de la recherche filtrée. Veuillez
supprimer tous les filtres
pour voir ces produits.
Ascentis™ Express 90 Å Biphenyl columns can be used for basic, acidic, or neutral compounds with alternate selectivity from C18 and is especially useful for separating peaks that elute early on C18 and other phenyl phases.
Kits include one cartridge, a stand-alone holder, a piece of tubing, and 2 nuts and ferrules. Guard cartridges require holders that are sold separately. The 2.1 and 4 mm I.D. cartridges use 21150AST or 59660-U (both stand-alone) or 504254 or 55205 (both integral). The 10 mm I.D. cartridges use 567499-U. The 21.2 mm I.D. cartridges use 581392-U.
Like their 5 micron siblings, 3 micron Zenix™ SEC columns feature a hydrophilic surface layer to prevent the sample from interacting with the underlying silica.
Used for the analyis or small scale purification of negatively charged biopolymers, such as glycoprotein isoforms, pegylated proteins and oligonucleotide.
SUPELCOSIL™ LC-ABZ phase has a unique deactivation technology which provides excellent reversed-phase performance for basic compounds, as well as those that are acidic, polar neutral, and non-polar.
This proficiency testing sample is produced in accordance with ISO/IEC 17043:2010. All information regarding the use of this material can be found in the reporting packet supplied for each sample.
The LC-SCX cation-exchange columns have strongly acidic propylsulfonic acid groups and are used for separating cations. Adjust pH, ionic strength, and organic modifier concentration to control retention and selectivity.
The bonded phase in Zenix™-C SEC columns is more polar than the hydrophilic phase used in Zenix™ columns, making Zenix™-C columns better suited for the gel filtration analysis of more hydrophobic bioopolymers such as membrane proteins and pegylated antibodies.
Due to a mixed retention mechanism, selectivity differences for polar groups are more pronounced than on C8 and C18 columns. C1 columns require 20-30% less organic modifier to provide retention similar to C18 columns.