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Features
- We validate our primary conjugates in functional applications, ensuring accurate and reliable results. Our flow cytometry conjugates undergo additional ICC/IF testing to confirm signal localization.
- Our validated fluorescent-conjugated antibodies eliminate the need for time-consuming in-house validation, enhancing efficiency in your research workflow. This enables you to dedicate more time to advance your research and achieve your objectives.
- Our fluorescence-conjugated primary antibodies ensure high specificity and accuracy in your results. They minimize the risk of false positives by eliminating the need for a secondary antibody, delivering more reliable outcomes.
- Fluorescently conjugated primary antibodies labeled using our Lightning-Link® technology provide a simple, efficient, and loss-free solution for generating high-quality reagents, ensuring consistent and reproducible staining in fluorescence-based applications.
Applications
- Our Alexa Fluor dyes provide brilliant and photostable signals, ideal for immunofluorescence (ICC/IF), immunohistochemistry (IHC), and flow cytometry.
- Our Phycoerythrin (R-PE) offers unmatched brightness, ensuring exceptional sensitivity in flow cytometry.
- Our FITC (fluorescein isothiocyanate) is a versatile and cost-effective choice for ICC/IF, IHC, and flow cytometry.
- APC (Allophycocyanin) delivers deep, rich fluorescence, ensuring superior performance in flow cytometry.
What are fluorophore-conjugated antibodies?
Fluorophore-conjugated antibodies are antibodies linked to fluorescent molecules, allowing researchers to detect and visualize specific targets in biological samples using fluorescence-based techniques such as flow cytometry, immunofluorescence, and immunohistochemistry. These antibodies provide high sensitivity and specificity by emitting fluorescence when exposed to a specific wavelength of light, allowing researchers to analyze protein expression, protein localization, cell populations, and biomolecular interactions.
How are fluorescently labeled antibodies produced?
Fluorescently labeled antibodies are produced by chemically conjugating a fluorophore to an antibody through covalent bonding, typically using reactive groups such as amine, thiol, or carboxyl linkages. This process ensures stable fluorescence emission while preserving the antibody’s specificity and binding affinity, enabling accurate detection of target antigens in various fluorescence-based applications.
What factors should be considered when choosing a fluorophore?
When choosing a fluorophore, key factors include its excitation and emission wavelengths, brightness, photostability, and compatibility with the detection instrument. Factors such as spectral overlap, quenching effects, and the specific application (eg, flow cytometry, immunofluorescence, or multiplexing) also play a crucial role in the selection of the optimal fluorophore for accurate and reliable results.
How are fluorescently labeled antibodies stored?
Follow the specific storage instructions provided on the datasheet for your antibody. If no specific guidance is available, store the antibody according to the general recommendations provided here. Fluorescently labeled antibodies should be stored at -20°C, as there is no significant advantage to storing them at -80°C, with aliquots frozen and thawed only once, and any remaining antibody kept at 4°C. For short-term storage of one to two weeks, 4°C is acceptable, but it is important to follow the datasheet recommendations and use aliquots no smaller than 10 μL to minimize concentration changes due to evaporation and adsorption. Before aliquoting, mix the antibody well to ensure homogeneity and maintain performance.