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Pyrene Probes

Cat# Name Structure M.W. Purity Pricing
AP129291-Ethynyl pyrene226.27≥ (95%) and 13C, TLC Pricing
AP106601-Pyrenecarboxylic Acid246.26≥95% Pricing
AP12935Pyrenebutyric acid288.34≥ (95%) Pricing
AP12932Pyrene hydrazide338.83≥ (95%) Pricing
AP10657N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)pyrene-1-carboxamide368.39≥95% Pricing
AP10579Propargyl-PEG2 Pyrene371.43≥95% Pricing
AP12936Pyrenebutyric acid NHS ester385.41≥ (95%) Pricing
AP10619N-Bicyclo[2.2.1]hept-5-en-2-ylmethyl-4-pyren-1-yl-butanamide393.52≥95% Pricing
AP12930Pyrene azide 1402.45≥ (95%) Pricing
AP10659N-(2-(bicyclo[2.2.1]hept-5-ene-2-carboxamido)ethyl)pyrene-1-carboxamide408.50≥95% Pricing
AP12933Pyrene maleimide410.47≥ (95%) Pricing
AP10578Propargyl-PEG3 Pyrene415.48≥95% Pricing
AP12931Pyrene azide 2416.47≥ (95%) Pricing
AP13822Pyrene-PEG3-azide448.5≥98% Pricing
AP13824Pyrene-PEG5-alcohol465.6≥98% Pricing
AP13472Pyrene-PEG4-acid495.6≥98% Pricing
AP13823Pyrene-PEG5-propargyl503.6≥98% Pricing
AP12937PEP azide544.64≥ (95%) Pricing
AP14243Pyrenebutyricamide-PEG5-amine, TFA salt550.70≥95% Pricing
AP10581Norbornene-PEG6 Pyrene714.90≥95% Pricing
AP13611Pyrene-PEG5-biotin690.856≥97% Pricing
AP15276Pyrene-PEG6-biotin734.9≥97% Pricing
AP10582Norbornene PEG7 Pyrene758.95≥95% Pricing
AP14244Pyrene Azide Plus802.70≥95% Pricing
AP12934Pyrene phosphoramidite dU955.04≥ (95%), 31P, Pricing

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    Pyrene in Bioconjugation: Features, Applications, and Quenching Experiments

    Pyrene is a polycyclic aromatic hydrocarbon with a distinct four-ring structure, widely used in bioconjugation for labeling biomolecules due to its strong blue fluorescence and unique quenching properties. Its hydrophobic nature and high quantum yield make it an ideal tool for studying molecular interactions, especially in environments of varying polarity.

    Key Features of Pyrene in Bioconjugation:

    • Pyrene Structure: Pyrene has a planar, aromatic structure with four fused benzene rings, which contributes to its strong fluorescence and ability to participate in non-covalent interactions.
    • Fluorescence Quenching and Polarity Sensitivity: Pyrene’s fluorescence is highly sensitive to its environment, particularly polarity. Quenching experiments with pyrene can reveal information about the local environment around the dye, such as changes in polarity or the presence of quenchers like oxygen or other molecules.
    • Excimer Formation: Pyrene can form excimers (excited state dimers) when two pyrene molecules are close, resulting in a red-shifted emission. This property is used to study the proximity of labeled biomolecules.
    • High Photostability: Pyrene resists photobleaching, making it ideal for long-term imaging and detection.

    Applications of Pyrene in Bioconjugation:

    • Fluorescent Probes: Pyrene-labeled probes are used to study molecular interactions, protein folding, and structural changes in biomolecules.
    • Quenching Experiments: Pyrene quenching experiments help investigate molecular environments, detect polarity changes, and study binding interactions. Quenching by specific quenchers, like nitroxides, or changes in solvent polarity, can provide insights into the local chemical environment.
    • Membrane Studies: Pyrene’s hydrophobic structure makes it useful for examining membrane fluidity, protein-lipid interactions, and microdomain organization.
    • Biochemical Assays: Pyrene conjugates detect proteins, nucleic acids, and other biomolecules with high sensitivity, leveraging excimer formation for dynamic interaction studies.

    Pyrene’s distinct structure, polarity-sensitive fluorescence, and quenching capabilities make it a powerful tool in bioconjugation, allowing researchers to explore complex biological environments and interactions with high precision and sensitivity.