Literature DB >> 12510000

Analysis of human alpha-thrombin by hydrophobic interaction high-performance liquid chromatography.

Göran Karlsson1.   

Abstract

The major active form of human thrombin, alpha-thrombin, was analyzed by hydrophobic interaction high-performance liquid chromatography (HIC-HPLC). The chromatographic system included a polymeric phenyl column and elution was performed by a gradient, 2-0M sodium chloride (5-20 min). Total analysis time was 30 min per injection. By this method, a good resolution between alpha-thrombin and the proteolytically modified thrombin forms, beta- and gamma-thrombin, was obtained. In addition, the thrombin preforms, prothrombin, prethrombin 1, and prethrombin 2, were also resolved from alpha-thrombin in the system. The results from the HIC method were compared to those obtained from non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis. By this high-resolution chromatographic method, the rapid analysis of purified alpha-thrombin is possible.

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Year:  2003        PMID: 12510000     DOI: 10.1016/s1046-5928(02)00596-x

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  1 in total

1.  Separation of proteins from human plasma by sample displacement chromatography in hydrophobic interaction mode.

Authors:  Djuro Josic; Lucas Breen; James Clifton; Martina Srajer Gajdosik; Dajana Gaso-Sokac; Marijana Rucevic; Egbert Müller
Journal:  Electrophoresis       Date:  2012-07       Impact factor: 3.535

  1 in total

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