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| ==Cold storage==
| | #REDIRECT [[Permeabilized muscle fibers]] |
| Small tissue samples (10 mg wet weight) should be put immediately into a pre-cooled storage medium, e.g. [[BIOPS]], and stored on ice (0 to 4 °C). Isolated mitochondria should be stored on ice in mitochondrial preservation medium.<ref name ="Gnaiger 2000 MitoInTheCold">[[Gnaiger 2000 MitoInTheCold|Gnaiger E, Kuznetsov AV, Schneeberger S, Seiler R, Brandacher G, Steurer W, Margreiter R (2000) Mitochondria in the cold. In: Life in the Cold (Heldmaier G, Klingenspor M, eds) Springer, Heidelberg, Berlin, New York: pp 431-442]].</ref>
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| ==Cold storage time==
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| Up to 12 hours of cold storage does normally not affect mitochondrial respiratory function of liver (pig: 24 h)<ref name ="Kuznetsov 2002 AnalytBiochem">[[Kuznetsov 2002 AnalytBiochem|Kuznetsov AV, Strobl D, Ruttmann E, Königsrainer A, Margreiter R, Gnaiger E (2002) Evaluation of mitochondrial respiratory function in small biopsies of liver. Analyt. Biochem. 305: 186-194]].</ref> and human muscle biopsies (skeletal muscle: 24 h<ref name ="Skladal 1994 BTK">[[Skladal 1994 BTK|Skladal D, Sperl W, Schranzhofer R, Krismer M, Gnaiger E, Margreiter R, Gellerich FN (1994) Preservation of mitochondrial functions in human skeletal muscle during storage in high energy preservation solution (HEPS). In: What is Controlling Life? (Gnaiger E, Gellerich FN, Wyss M, eds) Modern Trends in BioThermoKinetics 3. Innsbruck Univ. Press: 268-271]].</ref>; cardiac muscle: 8-12 h<ref name ="Lemieux 2011 IJBCB">[[Lemieux 2011 IJBCB|Lemieux H, Semsroth S, Antretter H, Hoefer D, Gnaiger E (2011) Mitochondrial respiratory control and early defects of oxidative phosphorylation in the failing human heart. Int. J. Biochem. Cell Biol. 43: 1729–1738]].</ref>).
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| Muscle biopsies of horses can be stored for 7 days without loss of function ([[MiPNet12.23 FibreRespiration]]).
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| Storage time without loss of function is, therefore, tissue and species dependent and should be evaluated experimentally. When a larger tissue sample is available, separate the sample into small (10 mg) pieces, and apply respirometric [[SUIT protocol]]s on subsamples in a time course. In particular, evaluate [[dyscoupling]] (''L/E'' and ''P/E'' coupling control ratios), cytochrome c release,<ref name ="Kuznetsov 2004 AJP">[[Kuznetsov 2004 AJP|Kuznetsov AV, Schneeberger S, Seiler R, Brandacher G, Mark W, Steurer W, Saks V, Usson Y, Margreiter R, Gnaiger E (2004) Mitochondrial defects and heterogeneous cytochrome ''c'' release after cardiac cold ischemia and reperfusion. Am. J. Physiol. Heart Circ. Physiol. 286: H1633–H1641]].</ref> and [[OXPHOS]] capacities with various substrate combinations.
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| ==References==
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| <references/>
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| {{#set: Scientific service =Quality Control|Permeabilized fibres }}
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| __SHOWFACTBOX__
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| {{Scientific service}}
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