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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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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. |
format | Online Article Text |
id | pubmed-4707181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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