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“The pure enzyme is stabilized by ethylenediaminetetraacetate and phosphate ion, but is rapidly inactivated in the presence of Mg++ or mercaptoethanol.”
The Journal of biological chemistry • 1969 | View Paper
“The fronting of the ATP peak resulting from the interference of magnesium ion in the enzyme assay buffer was suppressed by the addition of sodium ethylenediaminetetraacetate to the sample solution.”