Literature DB >> 3258151

The separation of myo-inositol phosphates by ion-pair chromatography.

J A Shayman1, D M BeMent.   

Abstract

The separation of myo-inositol phosphates by ion pair, reverse-phase high performance liquid chromatography has been investigated. The retention of the inositol phosphates is dependent on both the polarity of the hetaeron utilized and on the pH of the solvent. A method is presented which permits the isocratic separation of multiple forms of inositol phosphates including isomers of myo-inositol trisphosphate. This method appears to be superior to the anion exchange based systems currently employed because of smaller retention volumes, the low ionic strength of the solvent employed, the absence of a requirement for reequilibration, and the ability to perform separations isocratically.

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Year:  1988        PMID: 3258151     DOI: 10.1016/0006-291x(88)90566-9

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  2 in total

1.  The inositol 1,4,5-trisphosphate receptor binding sites of platelet membranes. pH-dependency, inhibition by polymeric sulphates, and the possible presence of arginine at the binding site.

Authors:  F O'Rourke; M B Feinstein
Journal:  Biochem J       Date:  1990-04-15       Impact factor: 3.857

2.  Automated isocratic high-performance liquid chromatography of inositol phosphate isomers.

Authors:  K A Wreggett; R F Irvine
Journal:  Biochem J       Date:  1989-09-15       Impact factor: 3.857

  2 in total

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