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Nonyl acridine orange *CAS 75168-11-5*

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Physical properties
Molecular weight472.5
SolventDMSO
Spectral properties
Excitation (nm)496
Emission (nm)519
Storage, safety and handling
Certificate of OriginDownload PDF
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
UNSPSC12352200

OverviewpdfSDSpdfProtocol


See also: Mitochondria
CAS
75168-11-5
Molecular weight
472.5
Excitation (nm)
496
Emission (nm)
519
10-n-Nonyl acridine orange (NAO) is a mitochondrial-specific fluorochrome. In contrast with Rh 123, NAO accumulation in the cell does not seem to be driven by the proton-motrice force but does seem to be related to specific interactions with mitochondrial membrane proteins and/or lipids. NAO uptake is independent of mitochondrial transmembrane potential. It is used to examine the changes in the mitochondrial compartment during the transfer of articular chondrocytes from cartilage to the culture conditions, where Rh 123 proves changes in mitochondrial activity and/or biogenesis. It is used for distinguishing mitochondrial activity from biogenesis. NAO and Rhodamine 123 (Rh 123) is a good pair of dyes for studying mitochondrial functions.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of Nonyl acridine orange *CAS 75168-11-5* to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM211.64 µL1.058 mL2.116 mL10.582 mL21.164 mL
5 mM42.328 µL211.64 µL423.28 µL2.116 mL4.233 mL
10 mM21.164 µL105.82 µL211.64 µL1.058 mL2.116 mL

Molarity calculator

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Spectrum


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Spectral properties

Excitation (nm)496
Emission (nm)519

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References


View all 15 references: Citation Explorer
Spectral studies of N-nonyl acridine orange in anionic, cationic and neutral surfactants
Authors: Wiosetek-Reske AM, Wysocki S.
Journal: Spectrochim Acta A Mol Biomol Spectrosc (2006): 1118
Determination of dipole moment in the ground and excited state by experimental and theoretical methods of N-nonyl acridine orange
Authors: Wiosetek-Reske AM, Wysocki S, Bak GW.
Journal: Spectrochim Acta A Mol Biomol Spectrosc (2005): 1172
Binding of 10-N-nonyl acridine orange to cardiolipin-deficient yeast cells: implications for assay of cardiolipin
Authors: Gohil VM, Gvozdenovic-Jeremic J, Schlame M, Greenberg ML.
Journal: Anal Biochem (2005): 350
Use of the fluorescent dye 10-N-nonyl acridine orange in quantitative and location assays of cardiolipin: a study on different experimental models
Authors: Garcia Fern, undefined and ez MI, Ceccarelli D, Muscatello U.
Journal: Anal Biochem (2004): 174
Intracellular distribution of the fluorescent dye nonyl acridine orange responds to the mitochondrial membrane potential: implications for assays of cardiolipin and mitochondrial mass
Authors: Jacobson J, Duchen MR, Heales SJ.
Journal: J Neurochem (2002): 224
Cardiolipin binds nonyl acridine orange by aggregating the dye at exposed hydrophobic domains on bilayer surfaces
Authors: Mileykovskaya E, Dowhan W, Birke RL, Zheng D, Lutterodt L, Haines TH.
Journal: FEBS Lett (2001): 187
Staining of mitochondrial membranes with 10-nonyl acridine orange, MitoFluor Green, and MitoTracker Green is affected by mitochondrial membrane potential altering drugs
Authors: Keij JF, Bell-Prince C, Steinkamp JA.
Journal: Cytometry (2000): 203
Visualization of phospholipid domains in Escherichia coli by using the cardiolipin-specific fluorescent dye 10-N-nonyl acridine orange
Authors: Mileykovskaya E, Dowhan W.
Journal: J Bacteriol (2000): 1172
Direct cardiolipin assay in yeast using the red fluorescence emission of 10-N-nonyl acridine orange
Authors: Gallet PF, Maftah A, Petit JM, Denis-Gay M, Julien R.
Journal: Eur J Biochem (1995): 113
10N-nonyl acridine orange interacts with cardiolipin and allows the quantification of this phospholipid in isolated mitochondria
Authors: Petit JM, Maftah A, Ratinaud MH, Julien R.
Journal: Eur J Biochem (1992): 267