Fluorimetric coupled enzyme assay for lysoplasmalogenase activity in liver.

We developed a continuous spectrofluorimetric assay of lysoplasmalogenase activity with the use of horse liver alcohol dehydrogenase as a coupling enzyme. In this method the disappearance of NADH is measured spectrofluorimetrically. The excitation and emission monochromators were set at 340 and 460...

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Bibliographic Details
Main Authors: Hirashima, Y, Farooqui, A A, Horrocks, L A
Format: Artigo
Language:Inglês
Published: 1989
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1138713/
https://ncbi.nlm.nih.gov/pubmed/2764893
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