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Organelle isolation: functional mitochondria from mouse liver, muscle and cultured fibroblasts.

Nature protocols (2007-04-05)
Christian Frezza, Sara Cipolat, Luca Scorrano
ZUSAMMENFASSUNG

Mitochondria participate in key metabolic reactions of the cell and regulate crucial signaling pathways including apoptosis. Although several approaches are available to study mitochondrial function in situ are available, investigating functional mitochondria that have been isolated from different tissues and from cultured cells offers still more unmatched advantages. This protocol illustrates a step-by-step procedure to obtain functional mitochondria with high yield from cells grown in culture, liver and muscle. The isolation procedures described here require 1-2 hours, depending on the source of the organelles. The polarographic analysis can be completed in 1 hour.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Magnesiumchlorid Hexahydrat, ACS reagent, 99.0-102.0%
Sigma-Aldrich
MOPS, ≥99.5% (titration)
Sigma-Aldrich
Antimycin A aus Streptomyces sp.
Sigma-Aldrich
Carbonylcyanid-4-(trifluormethoxy)phenylhydrazon, ≥98% (HPLC), powder
Sigma-Aldrich
Rotenon, ≥95%
Sigma-Aldrich
Ethylendiamintetraessigsäure Dinatriumsalz Dihydrat, reagent grade, 98.5-101.5% (titration)
Sigma-Aldrich
L-(−)-Maleinsäure, ≥95% (titration)
Sigma-Aldrich
Bernsteinsäure, BioXtra, BioRenewable, ≥99.0%