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.
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The bonded phase in SRT™-C SEC columns is more polar than the hydrophilic phase used in SRT™ columns, making SRT™-C columns better suited for the gel filtration analysis of more hydrophobic bioopolymers such as membrane proteins and pegylated antibodies.
TSKgel G5000HXL Columns are packed with rigid, porous, polymer beads. They are applied to the non-aqueous separation of polymers with molecular weights less than 4,000,000 Da.
TSKgel™ SuperHZM-H Mixed-Bed Columns are packed with rigid, porous, polymer beads each having a varying mean pore diameter. They are used for the non-aqueous separation of organic-soluble polymers with high molecular weights of less than 400,000,000 Da.
TSKgel MultiporeHxl-M Columns are packed with rigid, polymer beads that have a large pore size distribution within each particle. For the analysis of organic-soluble industrial polymers.
Resolve polar and nonpolar compounds in a single run. These columns have high pH stability (pH 1.5–10) in the separation of basic, neutral, and acidic species.
Ideal for analysis of hydroxy acids, like lactic, malic, tartaric and mandelic acids, amino acids, other amines and bi-functional racemates, like amino alcohols.
BIOshell™ Glycan HPLC Columns are specifically engineered to deliver fast, high resolution, reproducible glycan identification using HILIC chromatography.
TSKgel™ G-Oligo-PW is designed for high resolution separations of aqueous nonionic and cationic oligomers, and oligosaccharides such as hydrolyzed cyclodextrins. Because of the presence of cationic groups on the gel matrix, this column is not suited for separating anionic polymers. The PEG and PEO calibration curve is identical to that of G2500PWxl.
TSKgel™ Phenyl-5PW RP columns are filled with 10 micron porous polymethacrylate particles, the surface of which is covered with a high density of phenyl groups that causes proteins to be retained in a low salt buffer mobile phase and requiring a solvent gradient for their elution, as is the protocol in reversed phase chromatography.