FlavAc
FlavAc is a fluorescent dye (with an excitation wavelength of 980 nm) for real-time in vivo imaging of lipid metabolism disorders, including early fatty liver disease and atherosclerotic plaques. FlavAc specifically integrates into endogenous lipoproteins, primarily low-density lipoprotein (LDL), and shows no brightness enhancement when bound to albumin. FlavAc forms aggregates in aqueous solutions, leading to fluorescence quenching; however, when integrated into lipoproteins, such aggregation decreases, forming stable fluorescent complexes with enhanced brightness. FlavAc can selectively illuminate LDL upon laser irradiation.
For research use only. We do not sell to patients.
- Formula: C73H64BF4N3O9S
- Molecular Weight:1246.17
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
FlavAc (1‑50 μM) binds to lipoproteins in serum, reaching binding equilibrium within 6 h at 37 °C; it also induces significant NIR‑II fluorescence enhancement in serum, plasma and lipoprotein samples, while no notable fluorescence enhancement is observed in albumin solution or PBS[1].
FlavAc shows NIR‑II fluorescence that colocalizes with lipoprotein bands in agarose gel electrophoresis[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Below is our recommended experimental protocol, which serves only as a guide and needs to be adjusted according to your specific requirements.
1. Stock Solution Preparation
1.1 Solvent: DMSO.
1.2 Recommended concentration: 1 mM.
2. Working Solution Preparation
2.3 Diluents: Mouse serum, albumin solution, HDL solution, LDL solution, fetal bovine serum, phosphate-buffered saline (PBS).
2.2 Working concentrations: 1 μM, 5 μM, 10 μM, 50 μM.
2.3 Notes: Adjust the working solution concentration as needed; prepare fresh before use.
3. Staining Procedures
3.1 Sample types[1]:
3.1.1 In vivo animal samples: Mice.
3.1.2 Ex vivo tissue samples: Isolated mouse aorta, harvested major organs.
3.2 Incubation conditions:
3.2.1 In vivo imaging: Administer intravenously at a dose of 0.6 μmol/kg or 2 mg/kg.
4. Control Setup
4.1 Negative controls: Mice fed a normal diet for fatty liver disease imaging; C57BL/6J mice for atherosclerotic plaque imaging.
4.2 Reference control: Dye solution in DMSO is used for fluorescence retention rate calculation.
4.3 Positive controls are used to validate the experimental system; blank controls are used to eliminate reagent fluorescence interference.
5. Detection and Analysis
5.1 Instruments:
5.1.1 NIR-II fluorescence imaging system with an excitation wavelength of 980 nm.
5.2 Result analysis:
5.2.1 Fluorescence localization: Accumulates in the liver, aortic arch plaques and hindlimb blood vessels of mice.
5.2.2 Color change: NIR-II fluorescence shows cyan/red signals in imaging.
5.2.3 Experimental results: In the fatty liver model, fluorescence intensity increased with increasing duration of high-fat diet; this probe enabled NIR-II imaging of atherosclerotic plaques in ApoE⁻/⁻ mice, with significantly higher fluorescence signals in the plaque region compared to normal vascular tissue.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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Molecular Weight 1246.17
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Formula C73H64BF4N3O9S
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SMILES
COC1=CC=CC(OC)=C1C2=[O+]C3=C(C(/C=C/C(CCC/4)=C(SCC(C(O)=O)NC(C)=O)C4=C\C=C5C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6OC(C9=C(OC)C=CC=C9OC)=C\5)=C2)C=CC(N(C%10=CC=CC=C%10)C%11=CC=CC=C%11)=C3.F[B-](F)(F)F
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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)