|
|
||||||||
Clinical Chemistry, Vol 25, 269-272, Copyright © 1979 by American Association for Clinical Chemistry
BF Howell, S McCune and R Schaffer
The pyruvate-to-lactate assay for determining lactate dehydrogenase (EC 1.1.1.27) can now yield linearity equal to or better than that obtained by the lactate-to-pyruvate assay. In addition, there are significant advantages to the pyruvate-to-lactate reaction: (a) a greater change in absorbance per unit time, which allows more accurate spectrophotometric readout; (b) lower reactant concentrations are required, which substantially reduces the cost per assay; (c) solid reagents are used to prepare the assay solution; and (d) reagent solutions are more stable. However, impurities present in commercial NADH preparations may substantially affect measured lactated dehydrogenase activities; therefore, a Standard Reference Material for NADH is being developed for issuance by the National Bureau of Standards.
The following articles in journals at HighWire Press have cited this article:
![]() |
W. Beil, M. L. Enss, S. Müller, B. Obst, K.-F. Sewing, and S. Wagner Role of vacA and cagA in Helicobacter pylori Inhibition of Mucin Synthesis in Gastric Mucous Cells J. Clin. Microbiol., June 1, 2000; 38(6): 2215 - 2218. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |