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Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel
The epithelial Na(+) channel (ENaC) is traditionally composed of three subunits, although non‐canonical expression has been found in various tissues including the vasculature, brain, lung, and dendritic cells of the immune system. Studies of ENaC structure and function have largely relied on heterol...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837423/ https://www.ncbi.nlm.nih.gov/pubmed/36636010 http://dx.doi.org/10.14814/phy2.15554 |
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author | Mutchler, Stephanie M. Shi, Shujie Whelan, Sarah Christine M. Kleyman, Thomas R. |
author_facet | Mutchler, Stephanie M. Shi, Shujie Whelan, Sarah Christine M. Kleyman, Thomas R. |
author_sort | Mutchler, Stephanie M. |
collection | PubMed |
description | The epithelial Na(+) channel (ENaC) is traditionally composed of three subunits, although non‐canonical expression has been found in various tissues including the vasculature, brain, lung, and dendritic cells of the immune system. Studies of ENaC structure and function have largely relied on heterologous expression systems, often with epitope‐tagged channel subunits. Relevant in vivo physiological studies have used ENaC inhibitors, mice with global or tissue specific knockout of subunits, and anti‐ENaC subunit antibodies generated by investigators or by commercial sources. Availability of well‐characterized, specific antibodies is imperative as we move forward in understanding the role of ENaC in non‐epithelial tissues where expression, subunit organization, and electrophysiological characteristics may differ from epithelial tissues. We report that a commonly used commercial anti‐α subunit antibody recognizes an intense non‐specific band on mouse whole kidney and lung immunoblots, which migrates adjacent to a less intense, aldosterone‐induced full length α‐subunit. This antibody localizes to the basolateral membrane of aquaporin 2 negative cells in kidney medulla. We validated antibodies against the β‐ and γ‐subunits from the same commercial source. Our work illustrates the importance of validation studies when using popular, commercially available anti‐ENaC antibodies. |
format | Online Article Text |
id | pubmed-9837423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98374232023-01-18 Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel Mutchler, Stephanie M. Shi, Shujie Whelan, Sarah Christine M. Kleyman, Thomas R. Physiol Rep Original Articles The epithelial Na(+) channel (ENaC) is traditionally composed of three subunits, although non‐canonical expression has been found in various tissues including the vasculature, brain, lung, and dendritic cells of the immune system. Studies of ENaC structure and function have largely relied on heterologous expression systems, often with epitope‐tagged channel subunits. Relevant in vivo physiological studies have used ENaC inhibitors, mice with global or tissue specific knockout of subunits, and anti‐ENaC subunit antibodies generated by investigators or by commercial sources. Availability of well‐characterized, specific antibodies is imperative as we move forward in understanding the role of ENaC in non‐epithelial tissues where expression, subunit organization, and electrophysiological characteristics may differ from epithelial tissues. We report that a commonly used commercial anti‐α subunit antibody recognizes an intense non‐specific band on mouse whole kidney and lung immunoblots, which migrates adjacent to a less intense, aldosterone‐induced full length α‐subunit. This antibody localizes to the basolateral membrane of aquaporin 2 negative cells in kidney medulla. We validated antibodies against the β‐ and γ‐subunits from the same commercial source. Our work illustrates the importance of validation studies when using popular, commercially available anti‐ENaC antibodies. John Wiley and Sons Inc. 2023-01-12 /pmc/articles/PMC9837423/ /pubmed/36636010 http://dx.doi.org/10.14814/phy2.15554 Text en © 2023 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Mutchler, Stephanie M. Shi, Shujie Whelan, Sarah Christine M. Kleyman, Thomas R. Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel |
title | Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel |
title_full | Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel |
title_fullStr | Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel |
title_full_unstemmed | Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel |
title_short | Validation of commercially available antibodies directed against subunits of the epithelial Na(+) channel |
title_sort | validation of commercially available antibodies directed against subunits of the epithelial na(+) channel |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9837423/ https://www.ncbi.nlm.nih.gov/pubmed/36636010 http://dx.doi.org/10.14814/phy2.15554 |
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