Literature DB >> 3496810

Enzymatic fluorometric assay for myo-inositol trisphosphate.

J A Shayman, A R Morrison, O H Lowry.   

Abstract

The determination of myo-inositol trisphosphate by an enzymatic fluorometric assay is presented. The method involves the acid extraction of water-soluble inositol polyphosphates followed by separation by anion-exchange chromatography. Samples are subsequently neutralized by passage over a Dowex Cl- resin and elution with lithium chloride. Samples are then desalted with ethanol. Following dephosphorylation with alkaline phosphatase, free myo-inositol is measured enzymatically via the NAD-dependent oxidation to scyllo-inosose with myo-inositol dehydrogenase. The efficiency of recovery, assay specificity, and an application to the measurement of inositol polyphosphates in hormone-stimulated tissue are discussed.

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Year:  1987        PMID: 3496810     DOI: 10.1016/0003-2697(87)90434-9

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  4 in total

1.  Growth hormone activates phospholipase C in proximal tubular basolateral membranes from canine kidney.

Authors:  S A Rogers; M R Hammerman
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

2.  Measurement of picomole amounts of any inositol phosphate isomer separable by h.p.l.c. by means of a bioluminescence assay.

Authors:  S A Prestwich; T B Bolton
Journal:  Biochem J       Date:  1991-03-15       Impact factor: 3.857

3.  Insulin-like growth factor II stimulates production of inositol trisphosphate in proximal tubular basolateral membranes from canine kidney.

Authors:  S A Rogers; M R Hammerman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

4.  Inositol trisphosphate has no direct effect on the contractile apparatus of skinned cardiac muscles.

Authors:  T M Nosek; P D Clein; R E Godt
Journal:  Pflugers Arch       Date:  1990-12       Impact factor: 3.657

  4 in total

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