Lauridsen 2019 Mitochondrion: Difference between revisions
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<small>Copyright ยฉ 2019. Published by Elsevier B.V.</small> | <small>Copyright ยฉ 2019. Published by Elsevier B.V.</small> | ||
|keywords=Bioenergetics, Cryopreservation, Immuno-detection, Oxidative phosphorylation | |keywords=Bioenergetics, Cryopreservation, Immuno-detection, Oxidative phosphorylation, 143B Human bone osteosarcoma cells | ||
|editor=[[Plangger M]], | |editor=[[Plangger M]], | ||
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|area=Respiration, Instruments;methods | |area=Respiration, Instruments;methods | ||
|injuries=Cryopreservation | |injuries=Cryopreservation | ||
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|additional= | |tissues=Other cell lines | ||
|preparations=Intact cells | |||
|enzymes=Complex I, Complex IV;cytochrome c oxidase | |||
|couplingstates=LEAK, ROUTINE, ET | |||
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Revision as of 11:54, 22 May 2019
Lauridsen PE, Rasmussen LJ, Desler C (2019) Mitochondrial oxidative phosphorylation capacity of cryopreserved cells. Mitochondrion [Epub ahead of print]. |
Lauridsen PE, Rasmussen LJ, Desler C (2019) Mitochondrion
Abstract: Defects in mitochondrial oxidative phosphorylation are a feature of many human diseases. To date, determination of oxidative phosphorylation has required fresh and live sample material and therefore also access to specialized equipment and trained personnel. Cryopreservation of samples is an attractive alternative, where samples can be collected and stored in an economic and practical fashion for later bulk assays. Here, we present an accurate, reliable method for estimating mitochondrial oxidative phosphorylation capacity of cryopreserved human cells. Broad adoption of this method will allow uncomplicated collection of samples and measurements of oxidative phosphorylation.
Copyright ยฉ 2019. Published by Elsevier B.V. โข Keywords: Bioenergetics, Cryopreservation, Immuno-detection, Oxidative phosphorylation, 143B Human bone osteosarcoma cells โข Bioblast editor: Plangger M
Labels: MiParea: Respiration, Instruments;methods
Stress:Cryopreservation Organism: Human Tissue;cell: Other cell lines Preparation: Intact cells Enzyme: Complex I, Complex IV;cytochrome c oxidase
Coupling state: LEAK, ROUTINE, ET Pathway: ROX
2019-05