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A system for coupled multiple-column separation of proteins
Authors:W Kopaciewicz  F E Regnier
Institution:Department of Biochemistry, Purdue University, West Lafayette, Indiana 47906
Abstract:Purification of proteins is commonly a multiple-step process involving size exclusion, ion exchange, affinity, hydrophobic, and other modes of chromatography. In an effort to circumvent the laborious process of collecting the solutes from each column and reintroducing them onto a second column, a valving system is described that directs the samples eluted from a high-performance liquid chromatographic column through a detector with a high-pressure cell into either a second column or into storage loops of a multiloop value. This multiloop value is referred to as a high-pressure fraction collector. After development of the first column is complete, a second solvent can be directed to the second column or high-pressure fraction collector to elute the solutes back through the detector and onto any other column in the system. The process of eluting a sample from a column through a single detector and directing it to the high-pressure fraction collector or any other column in the system may be repeated a number of times. Such valving systems make it possible to chromatograph a single protein component on two or three columns in a short time.
Keywords:SEC  size-exclusion chromatography  AEC  anion-exchange chromatography  CEC  cation-exchange chromatography  RPC  reverse-phase chromatography  nSEC  nonideal size-exclusion chromatography  IEC  ion-exchange chromatography  OVA  ovalbumin  BSA  bovine serum albumin
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