Sensitive Microtiter Assays for NAD, NADP and Protein Quantification in Human Lymphocytes

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Intracellular levels of NAD are of renewed interest in clinical and basic science research due to the new discovery of enzymes which utilize NAD as a substrate. Microtiter assays for the determination of NAD, NADP and protein were developed as modifications of previously published methods. The resulting assays are simple, cost effective and sensitive. An improved method of isolating lymphocytes was also developed. The resultant procedure requires one hour and removes greater than 99.9% of the platelets. Lymphocyte pools were stabilized with the addition of ADP-ribosyltransferase inhibitors and a modified extraction procedure. These studies have led to the development of … continued below

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viii, 93, [1] leaves : ill.

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Johnson, James, 1964- May 1990.

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  • Johnson, James, 1964-

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Intracellular levels of NAD are of renewed interest in clinical and basic science research due to the new discovery of enzymes which utilize NAD as a substrate. Microtiter assays for the determination of NAD, NADP and protein were developed as modifications of previously published methods. The resulting assays are simple, cost effective and sensitive. An improved method of isolating lymphocytes was also developed. The resultant procedure requires one hour and removes greater than 99.9% of the platelets. Lymphocyte pools were stabilized with the addition of ADP-ribosyltransferase inhibitors and a modified extraction procedure. These studies have led to the development of a method for evaluation of NAD in human lymphocytes that is sensitive, selective and suitable for automation.

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viii, 93, [1] leaves : ill.

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  • May 1990

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  • March 9, 2015, 8:15 a.m.

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  • Oct. 23, 2017, 3:21 p.m.

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Johnson, James, 1964-. Sensitive Microtiter Assays for NAD, NADP and Protein Quantification in Human Lymphocytes, thesis, May 1990; Denton, Texas. (https://digital.library.unt.edu/ark:/67531/metadc501179/: accessed May 28, 2024), University of North Texas Libraries, UNT Digital Library, https://digital.library.unt.edu; .

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