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

Hypobaric hypoxia modulated structural characteristics of circulating cell-free DNA in high-altitude pulmonary edema.

American journal of physiology. Lung cellular and molecular physiology·2024
Same author

Differential methylation in EGLN1 associates with blood oxygen saturation and plasma protein levels in high-altitude pulmonary edema.

Clinical epigenetics·2022
Same author

The deleterious impact of a non-synonymous SNP on protein structure and function is apparent in hypertension.

Journal of molecular modeling·2021
Same author

Susceptibility of CTLA-4 -1661A/G polymorphism towards severity of rheumatic heart disease.

Indian heart journal·2021
Same author

High-altitude pulmonary edema is aggravated by risk loci and associated transcription factors in HIF-prolyl hydroxylases.

Human molecular genetics·2021
Same author

Vascular homeostasis at high-altitude: role of genetic variants and transcription factors.

Pulmonary circulation·2020

Related Experiment Video

Updated: May 17, 2026

Fast and Accurate Exhaled Breath Ammonia Measurement
06:27

Fast and Accurate Exhaled Breath Ammonia Measurement

Published on: June 11, 2014

A rapid method for plasma ammonia estimation using an indigenously purified enzyme.

M A Qadar Pasha1, R B Ram, M D Gupta

  • 1Centre for Biochemical Technology, Mall Road, 110007 Delhi.

Indian Journal of Clinical Biochemistry : IJCB
|October 30, 2012
PubMed
Summary

This study developed a rapid blood ammonia assay for diagnosing liver disease. The new method is stable, sensitive, and suitable for routine clinical use.

Keywords:
Ammoniadeaminase inhibitorenzymatic assayglutamate dehydrogenase

More Related Videos

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O
08:05

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O

Published on: October 7, 2020

Workflow Based on the Combination of Isotopic Tracer Experiments to Investigate Microbial Metabolism of Multiple Nutrient Sources
12:47

Workflow Based on the Combination of Isotopic Tracer Experiments to Investigate Microbial Metabolism of Multiple Nutrient Sources

Published on: January 22, 2018

Related Experiment Videos

Last Updated: May 17, 2026

Fast and Accurate Exhaled Breath Ammonia Measurement
06:27

Fast and Accurate Exhaled Breath Ammonia Measurement

Published on: June 11, 2014

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O
08:05

Measurement of the Potential Rates of Dissimilatory Nitrate Reduction to Ammonium Based on 14NH4+/15NH4+ Analyses via Sequential Conversion to N2O

Published on: October 7, 2020

Workflow Based on the Combination of Isotopic Tracer Experiments to Investigate Microbial Metabolism of Multiple Nutrient Sources
12:47

Workflow Based on the Combination of Isotopic Tracer Experiments to Investigate Microbial Metabolism of Multiple Nutrient Sources

Published on: January 22, 2018

Area of Science:

  • Clinical Chemistry
  • Biochemical Diagnostics
  • Enzymology

Background:

  • Accurate determination of blood ammonia levels is crucial for diagnosing hepatic disorders.
  • Existing methods may require optimization for clinical settings.

Purpose of the Study:

  • To standardize and validate a novel enzymatic assay for blood ammonia determination.
  • To assess the assay's performance characteristics and suitability for routine clinical use.

Main Methods:

  • Utilized an indigenously purified enzyme for assay standardization.
  • Employed a two-reagent system with a 5-minute reaction time at 25-27°C.
  • Conducted performance evaluations including linearity, imprecision, functional sensitivity, and interference studies.

Main Results:

  • The assay demonstrated stability for at least one year with lyophilized reagents.
  • Plasma ammonia levels were significantly higher in patients with hepatic disorders (69.1±32.4 μMol/L) compared to controls (13.7±7.3 μMol/L).
  • Functional sensitivity ranged from 2-1000 μMol/L with low coefficients of variation (1.1-3.7%).

Conclusions:

  • The developed enzymatic assay is reliable, sensitive, and stable for quantifying blood ammonia.
  • The assay's rapid turnaround time and broad measurement range make it ideal for routine clinical diagnostics of hepatic disorders.