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Quality Segment
manufacturer/tradename
Chemicon®, MitoLight
technique(s)
flow cytometry: suitable
detection method
fluorometric
shipped in
dry ice
General description
MitoLight partitions differently in healthy cells than in apoptotic cells. Therefore, it has been possible to use a fluorescence ratioing technique to study mitochondrial membrane potentials. In healthy cells, the dye accumulates and aggregates in the mitochondria, giving off a bright red fluorescence (λem = 585-590 nm). In apoptotic cells with altered mitochondrial membrane potential, the dye in its monomeric form stays in the cytoplasm, fluorescing green (λem = 527-530 nm), providing a ready discrimination between apoptotic and nonapoptotic cells. The fluorescence can be observed by fluorescence microscopy using a band-pass filter (detects FITC and rhodamine) or analyzed by flow cytometry using FITC channel for green monomers (Ex/Em = 488/530) and PI channel for red aggregates (Ex/Em = 488/585).
For research use only; Not for use in diagnostic procedures
Application
Apoptosis & Cancer
Preparation Note
PROTECT REAGENTS FROM LIGHT.
Other Notes
10X Incubation Buffer (Part No. 71614): 20 mL.
Legal Information
Disclaimer
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