TSKgel^® Ether-5PW HPLC Column

32110501

Both hydrophobic interaction chromatography (HIC) and reversed-phase liquid chromatography separate on the basis of protein hydrophobicity and allow selective binding and desorption of proteins. However, HIC operates at significantly lower binding energy and uses aqueous mobile phases. These characteristics provide a gentle technique that is less likely to disturb protein conformation. As a result, HIC generally provides better activity recovery.
Three resin-based TSKgel HIC columns provide a range of hydrophobicities for chromatographic optimization. TSKgel Phenyl-5PW columns are most hydrophobic, followed by Ether-5PW, while the surface of Butyl-NPR columns is most polar or least hydrophobic. Ammonium sulfate concentration can be minimized by using a more hydrophobic packing such as Phenyl-5PW. We recommend the more polar Ether-5PW column for purifying more hydrophobic proteins. Ether-5PW and Phenyl-5PW packings are based on TSKgel G5000PW resin - 10 micron particles with 1000  pores. Butyl-NPR packing is prepared from 2.5 micron nonporous particles, allowing for rapid analyses and semi-micropreparative applications. All three column types can be cleaned with 0.2 M NaOH. Scale-up can be performed by using corresponding Toyopearl bulk resins.
Among the TSKgel HIC columns, TSKgel Ether-5PW has intermediate hydrophobity. It is an excellent choice for separating hydrophobic molecules such as membrane proteins or monoclonal antibodies such as IgG or IgM. Featuring a 1000 A pore size in a polymethacrylate base material, the Ether-5PW column is stable in either acid or caustic cleaning regimens and provides excellent access to larger molecules with low diffusion coefficients.

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TSKgel is a registered trademark of Tosoh Corporation

stainless steel hardware

TSKgel^®

Tosoh 18760

≤4 M salt concentration
≤50% organic solvent
0.12 mL/min flow rate
10-50 ℃ temperature
6 bar max. pressure

HPLC: suitable

7.5 cm × 2 mm

polymer particle platform

ether phase

10 μm

1000 Å

2 - 12

hydrophobic interaction (HIC)