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Data supporting the spectrophotometric method for the estimation of catalase activity

Here we provide raw and processed data and methods for the estimation of catalase activities. The method for presenting a simple and accurate colorimetric assay for catalase activities is described. This method is based on the reaction of undecomposed hydrogen peroxide with ammonium molybdate to pro...

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Detalles Bibliográficos
Autores principales: Hadwan, Mahmoud Hussein, Abed, Hussein Najm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707181/
https://www.ncbi.nlm.nih.gov/pubmed/26862558
http://dx.doi.org/10.1016/j.dib.2015.12.012
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author Hadwan, Mahmoud Hussein
Abed, Hussein Najm
author_facet Hadwan, Mahmoud Hussein
Abed, Hussein Najm
author_sort Hadwan, Mahmoud Hussein
collection PubMed
description Here we provide raw and processed data and methods for the estimation of catalase activities. The method for presenting a simple and accurate colorimetric assay for catalase activities is described. This method is based on the reaction of undecomposed hydrogen peroxide with ammonium molybdate to produce a yellowish color, which has a maximum absorbance at 374 nm. The method is characterized by adding a correction factor to exclude the interference that arises from the presence of amino acids and proteins in serum. The assay acts to keep out the interferences that arose from measurement of absorbance at unsuitable wavelengths.
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spelling pubmed-47071812016-02-09 Data supporting the spectrophotometric method for the estimation of catalase activity Hadwan, Mahmoud Hussein Abed, Hussein Najm Data Brief Data Article Here we provide raw and processed data and methods for the estimation of catalase activities. The method for presenting a simple and accurate colorimetric assay for catalase activities is described. This method is based on the reaction of undecomposed hydrogen peroxide with ammonium molybdate to produce a yellowish color, which has a maximum absorbance at 374 nm. The method is characterized by adding a correction factor to exclude the interference that arises from the presence of amino acids and proteins in serum. The assay acts to keep out the interferences that arose from measurement of absorbance at unsuitable wavelengths. Elsevier 2015-12-17 /pmc/articles/PMC4707181/ /pubmed/26862558 http://dx.doi.org/10.1016/j.dib.2015.12.012 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Hadwan, Mahmoud Hussein
Abed, Hussein Najm
Data supporting the spectrophotometric method for the estimation of catalase activity
title Data supporting the spectrophotometric method for the estimation of catalase activity
title_full Data supporting the spectrophotometric method for the estimation of catalase activity
title_fullStr Data supporting the spectrophotometric method for the estimation of catalase activity
title_full_unstemmed Data supporting the spectrophotometric method for the estimation of catalase activity
title_short Data supporting the spectrophotometric method for the estimation of catalase activity
title_sort data supporting the spectrophotometric method for the estimation of catalase activity
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707181/
https://www.ncbi.nlm.nih.gov/pubmed/26862558
http://dx.doi.org/10.1016/j.dib.2015.12.012
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