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H-FluNox is a selective fluorescent probe designed to detect labile heme by triggering fluorescence through a biomimetic deoxygenation reaction with nitrogen oxides. Its selectivity for labile heme is over 100 times higher than for Fe(II), enabling it to distinguish labile heme from the unstable Fe(II) pool in live cells. H-FluNox is sensitive enough to detect subcellular labile heme. (λex=490 nm, λem=535 nm)

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | H-FluNox is a selective fluorescent probe designed to detect labile heme by triggering fluorescence through a biomimetic deoxygenation reaction with nitrogen oxides. Its selectivity for labile heme is over 100 times higher than for Fe(II), enabling it to distinguish labile heme from the unstable Fe(II) pool in live cells. H-FluNox is sensitive enough to detect subcellular labile heme. (λex=490 nm, λem=535 nm) |
| Molecular Weight | 451.42 |
| Formula | C25H19F2NO5 |
| Cas No. | 2897614-59-2 |
| Smiles | O=C1OC2(C3=CC=C(O)C=C3OC4=CC(=CC=C42)N5(=O)CCC(F)(F)CC5)C=6C=CC=CC16 |
| Storage | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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