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Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue
OPA1 is a dynamin-related GTPase that modulates various mitochondrial functions and is involved in mitochondrial morphology. There are eight different isoforms of OPA1 in humans and five different isoforms in mice that are expressed as short or long-form isoforms. These isoforms contribute to OPA1’s...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245902/ https://www.ncbi.nlm.nih.gov/pubmed/37292669 http://dx.doi.org/10.1101/2023.05.20.541601 |
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author | Stephens, Dominique C. Mungai, Margaret Crabtree, Amber Beasley, Heather K. Garza-Lopez, Edgar Neikirk, Kit Bacevac, Serif Vang, Larry Vue, Zer Vue, Neng Marshall, Andrea G. Turner, Kyrin Shao, Jianqiang Murray, Sandra Gaddy, Jennifer A. Wanjalla, Celestine Davis, Jamaine Damo, Steven Hinton, Antentor O. |
author_facet | Stephens, Dominique C. Mungai, Margaret Crabtree, Amber Beasley, Heather K. Garza-Lopez, Edgar Neikirk, Kit Bacevac, Serif Vang, Larry Vue, Zer Vue, Neng Marshall, Andrea G. Turner, Kyrin Shao, Jianqiang Murray, Sandra Gaddy, Jennifer A. Wanjalla, Celestine Davis, Jamaine Damo, Steven Hinton, Antentor O. |
author_sort | Stephens, Dominique C. |
collection | PubMed |
description | OPA1 is a dynamin-related GTPase that modulates various mitochondrial functions and is involved in mitochondrial morphology. There are eight different isoforms of OPA1 in humans and five different isoforms in mice that are expressed as short or long-form isoforms. These isoforms contribute to OPA1’s ability to control mitochondrial functions. However, isolating OPA1 all long and short isoforms through western blot has been a difficult task. To address this issue, we outline an optimized western blot protocol to isolate 5 different isoforms of OPA1 on the basis of different antibodies. This protocol can be used to study changes in mitochondrial structure and function. |
format | Online Article Text |
id | pubmed-10245902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-102459022023-06-08 Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue Stephens, Dominique C. Mungai, Margaret Crabtree, Amber Beasley, Heather K. Garza-Lopez, Edgar Neikirk, Kit Bacevac, Serif Vang, Larry Vue, Zer Vue, Neng Marshall, Andrea G. Turner, Kyrin Shao, Jianqiang Murray, Sandra Gaddy, Jennifer A. Wanjalla, Celestine Davis, Jamaine Damo, Steven Hinton, Antentor O. bioRxiv Article OPA1 is a dynamin-related GTPase that modulates various mitochondrial functions and is involved in mitochondrial morphology. There are eight different isoforms of OPA1 in humans and five different isoforms in mice that are expressed as short or long-form isoforms. These isoforms contribute to OPA1’s ability to control mitochondrial functions. However, isolating OPA1 all long and short isoforms through western blot has been a difficult task. To address this issue, we outline an optimized western blot protocol to isolate 5 different isoforms of OPA1 on the basis of different antibodies. This protocol can be used to study changes in mitochondrial structure and function. Cold Spring Harbor Laboratory 2023-08-19 /pmc/articles/PMC10245902/ /pubmed/37292669 http://dx.doi.org/10.1101/2023.05.20.541601 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Stephens, Dominique C. Mungai, Margaret Crabtree, Amber Beasley, Heather K. Garza-Lopez, Edgar Neikirk, Kit Bacevac, Serif Vang, Larry Vue, Zer Vue, Neng Marshall, Andrea G. Turner, Kyrin Shao, Jianqiang Murray, Sandra Gaddy, Jennifer A. Wanjalla, Celestine Davis, Jamaine Damo, Steven Hinton, Antentor O. Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue |
title | Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue |
title_full | Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue |
title_fullStr | Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue |
title_full_unstemmed | Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue |
title_short | Creating Optimal Conditions for OPA1 Isoforms by Western Blot in Skeletal Muscle Cells and Tissue |
title_sort | creating optimal conditions for opa1 isoforms by western blot in skeletal muscle cells and tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245902/ https://www.ncbi.nlm.nih.gov/pubmed/37292669 http://dx.doi.org/10.1101/2023.05.20.541601 |
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