Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Novel reference method for precise determination of tryptophanase activity.

Biology methods & protocols·2026
Same author

Sensitive and specific fluorometric assay for assessment of glyoxalase II enzymatic activity in microbial samples and biological tissue.

Enzyme and microbial technology·2025
Same author

Enhanced protocol for measuring glutathione peroxidase activity using a new glutathione peroxidase-Tiron assay.

Biology methods & protocols·2025
Same author

Simplified and economic measurement of glyoxalase I activity using 2,4-dinitrophenylhydrazine: A valuable tool for researchers.

Biology methods & protocols·2025
Same author

An improved method for measuring catalase activity in biological samples.

Biology methods & protocols·2024
Same author

Fluorometric Protocol for Estimating Peroxiredoxin Activity in Biological Tissues.

Journal of fluorescence·2022

Related Experiment Video

Updated: Jun 11, 2025

Bergmeyer Glucose Quantification for Microbiological Samples
07:23

Bergmeyer Glucose Quantification for Microbiological Samples

Published on: January 17, 2025

416

A new method for quantifying glyoxalase II activity in biological samples.

Mohammed Alaa Kadhum1, Mahmoud Hussein Hadwan1

  • 1Department of Chemistry, College of Science, University of Babylon, Hillah City 51002, Iraq.

Biology Methods & Protocols
|October 1, 2024
PubMed
Summary

A new 2,4-dinitrophenylhydrazine (2,4-DNPH) assay accurately measures Glyoxalase II (Glo II) activity. This simple, cost-effective method offers a reliable alternative for Glo II enzyme research and diagnostics.

Keywords:
Bland–Altman plotDNPH methodglyoxalase systemmedical applicationmethylglyoxal

More Related Videos

Author Spotlight: Innovating Thiol Quantification and Biomarker Detection for Oxidative Stress Research
03:35

Author Spotlight: Innovating Thiol Quantification and Biomarker Detection for Oxidative Stress Research

Published on: June 28, 2024

1.2K
Synthesis of Indoxyl-glycosides for Detection of Glycosidase Activities
09:10

Synthesis of Indoxyl-glycosides for Detection of Glycosidase Activities

Published on: May 27, 2015

6.6K

Related Experiment Videos

Last Updated: Jun 11, 2025

Bergmeyer Glucose Quantification for Microbiological Samples
07:23

Bergmeyer Glucose Quantification for Microbiological Samples

Published on: January 17, 2025

416
Author Spotlight: Innovating Thiol Quantification and Biomarker Detection for Oxidative Stress Research
03:35

Author Spotlight: Innovating Thiol Quantification and Biomarker Detection for Oxidative Stress Research

Published on: June 28, 2024

1.2K
Synthesis of Indoxyl-glycosides for Detection of Glycosidase Activities
09:10

Synthesis of Indoxyl-glycosides for Detection of Glycosidase Activities

Published on: May 27, 2015

6.6K

Area of Science:

  • Biochemistry
  • Enzymology

Background:

  • Glyoxalase II (Glo II) is essential for detoxifying harmful metabolites and maintaining cellular redox balance.
  • Dysregulation of Glo II is implicated in diseases like cancer and diabetes.

Purpose of the Study:

  • To develop and validate a novel, cost-effective method for measuring Glyoxalase II activity using 2,4-dinitrophenylhydrazine (2,4-DNPH).

Main Methods:

  • The assay utilizes the reaction between 2,4-DNPH and pyruvate, a product of the Glo II-catalyzed reaction, to form a colored hydrazone complex.
  • Absorbance is measured at 430 nm to quantify Glo II activity.
  • The method was validated for stability, sensitivity, linearity, and interference resistance.

Main Results:

  • The 2,4-DNPH method demonstrated high stability, sensitivity, and linearity.
  • It showed strong correlation with the existing UV method for Glo II activity measurement.
  • The assay proved resistant to interference from various biochemical substances.

Conclusions:

  • The 2,4-DNPH assay provides a simple, accurate, and cost-effective means to measure Glo II activity.
  • This novel method is suitable for diverse laboratory settings, including research and clinical diagnostics.
  • It holds potential for advancing research and applications in diseases linked to Glo II dysregulation.