MitoAIE1
MitoAIE1 is a Fluorescent probe for mitochondrial viscosity detection. MitoAIE1 contains a pyridinium structural unit, which endows it with mitochondria-targeting specificity. The detection mechanism of this probe is based on aggregation-induced emission (AIE): in low-viscosity media such as PBS buffer, intramolecular rotation leads to non-radiative energy dissipation, resulting in only weak fluorescence; however, in high-viscosity environments such as the mitochondrial matrix or the vicinity of the inner mitochondrial membrane, such intramolecular motion is restricted, thereby significantly enhancing its fluorescent signal; in addition, this probe is not interfered by changes in microenvironment polarity and pH. Its emission wavelength is 625 nm, with absorption peaks at 325 nm and 450 nm; when transferred from low-viscosity PBS to high-viscosity 99% glycerol, its fluorescence intensity at 625 nm can be increased by 38-fold. It can be used to monitor changes in mitochondrial viscosity during processes such as Stauroporine (HY-15141)-induced apoptosis and starvation-induced mitophagy in live cells, and has good biocompatibility.
For research use only. We do not sell to patients.
- CAS No.: 2246946-49-4
- Formula: C42H36I2N2O2
- Molecular Weight:854.56
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Guidelines (The following is a recommended experimental protocol for guidance only, and adjustments are required based on your specific needs)[1].
1. Stock Solution Preparation
1.2 Concentration recommendation: 40 μM.
2. Staining Procedure
2.1 Sample type: Adherent cells (HeLa cells)
2.1.1 Adherent cells: No trypsinization step is specified for staining.
2.2 Incubation conditions: Incubate with 40 μM MitoAIE1.
2.3 Washing step: No washing step is specified.
3. Detection and Analysis
3.1 Instrument: Confocal fluorescence microscope.
3.1.1 Excitation/emission wavelength: The emission wavelength is 625 nm.
3.2 Result analysis:
3.2.1 Changes in fluorescence intensity: The fluorescence is weak in low-viscosity medium (PBS); the fluorescence intensity increases 38-fold in high-viscosity medium (99% glycerol). The fluorescence intensity increases during staurosporine-induced apoptosis and starvation-induced mitophagy.
3.2.2 Fluorescence localization: It specifically accumulates in mitochondria, with the fluorescence signal overlapping with that of Mito-Tracker green (Pearson correlation coefficient = 0.93).
5.2.3 Color change: Red fluorescence.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 2246946-49-4
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Molecular Weight 854.56
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Formula C42H36I2N2O2
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SMILES
C[N+]1=CC=C(C=C1)/C=C/C2=CC=C(/C(C3=CC=C(O)C=C3)=C(C4=CC=C(O)C=C4)\C5=CC=C(/C=C/C6=CC=[N+](C=C6)C)C=C5)C=C2.[I-].[I-]
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
- MitoAIE1
- 2246946-49-4
- MitoAIE 1
- MitoAIE-1
- Fluorescent Dye
- Mitochondrial Metabolism
- HeLa cells
- mitochondrial matrix
- confocal fluorescence microscope
- stauroporine-induced apoptosis
- mitochondrial viscosity
- inner mitochondrial membrane
- Mito-Tracker green
- pyridium moiety
- aggregation-induced emission
- starvation-induced mitophagy
- Inhibitor
- inhibitor
- inhibit