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diseases. G-CSF is crucial for recovering white blood cell counts after chemotherapy. IFNs like interferon-beta have<br />

antiviral and anti-inflammatory applications. Animal-free versions cater to applications where the absence of<br />

animal-derived components is critical, ensuring ethical and controlled use. This distinguishes them from cGMPproduced<br />

cytokines. Reach out to us for specific details tailored to meet your research needs.<br />

TR-FRET<br />

Time-Resolved Fluorescence Resonance Energy Transfer<br />

(TR-FRET) is a powerful and versatile molecular assay<br />

technique used in biological research and drug discovery.<br />

TR-FRET allows scientists to study molecular interactions<br />

and events within cells or biochemical reactions with high<br />

sensitivity and precision. It is particularly valuable for<br />

measuring protein-protein interactions, receptor-ligand<br />

binding, and various other biomolecular processes.<br />

TR-FRET relies on the principles of fluorescence resonance<br />

energy transfer (FRET), in which energy is transferred from<br />

one fluorophore (the donor) to another (the acceptor)<br />

when they are in close proximity, typically within 10-100<br />

angstroms. The key distinction in TR-FRET is the measurement of the time delay between excitation and emission, which<br />

eliminates short-lived background fluorescence and significantly enhances signal-to-noise ratios.<br />

To perform TR-FRET assays, researchers require specific reagents:<br />

• Donor and Acceptor Fluorophores: These are the fluorescent molecules that emit light when excited by an energy<br />

source. The donor fluorophore, typically a lanthanide chelate (e.g., Europium or Terbium), is excited by a pulsed<br />

light source, and its emission is transferred to the acceptor fluorophore (e.g., XL665 or APC), resulting in a FRET<br />

signal.<br />

• Target Molecules: These are the biological components under investigation, such as proteins, nucleic acids, or<br />

small molecules, labeled with the donor or acceptor fluorophores. The choice of labeling strategy depends on the<br />

specific experiment and the accessibility of the target sites.<br />

• Buffer Solutions: Appropriate buffer solutions are used to maintain physiological conditions and optimize the<br />

stability of the labeled molecules.<br />

• Time-Resolved Detection System: This includes a fluorescence plate reader or a dedicated TR-FRET reader<br />

equipped with the capability to measure the time delay between excitation and emission of the fluorophores.<br />

TR-FRET has revolutionized the field of molecular biology and drug discovery by enabling the study of complex cellular<br />

processes in a high-throughput and sensitive manner. Researchers can use TR-FRET to assess biomolecular interactions,<br />

screen for potential drug candidates, and gain insights into cellular pathways and mechanisms with exceptional accuracy<br />

and efficiency.<br />

Europium chelates<br />

Europium chelates are a class of luminescent compounds widely used in various applications, particularly in the field of<br />

fluorescence-based assays and diagnostics. These chelates consist of europium ions (Eu3+) bound to organic chelating<br />

ligands, which enhance their stability and luminescent properties. Europium ions are known for their unique photophysical<br />

properties, including a long fluorescence lifetime, narrow emission bands, and resistance to photobleaching. These features<br />

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