The Alexa Fluor family of fluorescent dyes is a series of dyes invented by Molecular Probes, now a part of Thermo Fisher Scientific, and sold under the Invitrogen brand name. Alexa Fluor dyes are frequently used as cell and tissue labels in fluorescence microscopy and cell biology.^[1] Alexa Fluor dyes can be conjugated directly to primary antibodies or to secondary antibodies to amplify signal and sensitivity^[2] or other biomolecules.^{[citation needed]}

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The excitation and emission spectra of the Alexa Fluor series cover the visible spectrum and extend into the infrared.^[3] The individual members of the family are numbered according roughly to their excitation maxima in nanometers.

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Richard and Rosaria Haugland, the founders of Molecular Probes, are well known in biology and chemistry for their research into fluorescent dyes useful in biological research applications.^{[according to whom?]} At the time that Molecular Probes was founded,^[when?] such products were largely unavailable commercially.^{[citation needed]} A number of fluorescent dyes that are now widely used were discovered and developed in the laboratories of Molecular Probes.^{[citation needed]}—dyes such as Texas Red, Cascade Blue, Oregon Green, Marina Blue, and the Alexa Fluor family.^{[citation needed]} The most famous of these, the Alexa Fluor family of dyes,^{[according to whom?]} were designed to improve upon properties of previously developed biological fluorescent dye families, and solve some of the issues that they possessed.^{[citation needed]} The Alexa Fluor dyes were named after Alex Haugland, son of Richard and Rosaria Haugland.^{[citation needed]}

Molecular Probes was acquired in 2003 by Invitrogen,^[4] who worked to further expand the Alexa Fluor family by the addition of new dyes to fill gaps not covered in the emission spectrum.^{[citation needed]} In 2008, Invitrogen and the Alexa Fluor product line became a part of the Life Technologies, after the Invitrogen merger with Applied Biosystems.^{[citation needed]} In 2014, Life Technologies was acquired by Thermo Fisher Scientific, who revitalized the Invitrogen name and brand, bringing the Alexa Fluor product line back under it.^{[citation needed]}

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The Alexa Fluor dyes were chemically synthesized through sulfonation and additional chemical modifications made to the well known families of coumarin, rhodamine, and cyanine dyes, and to the xanthene family (of which the fluorescein, an industry-standard, is a part).^{[citation needed]} Sulfonation made the product Alexa Fluor dyes negatively charged and thus more hydrophilic and soluble than their parent dyes;^{[citation needed]} the additional modifications were aimed to improve dye performance in other areas.^{[citation needed]} For example, Alexa Fluor 488, a sulfonated and otherwise chemically modified^{[clarification needed]} form of fluorescein, was designed to solve the well known issues of rapid photobleaching and pH-dependent fluorescent intensity characteristic of the dye fluorescein isothiocyanate.^{[citation needed]}

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The Alexa Fluor series dyes are less pH-sensitive and more photostable than the original dyes (fluorescein, rhodamine, etc.) from which they were synthesized.^{[citation needed]} While extinction coefficients of each member of this line of dyes are known (see table), quantum yields^{[clarification needed]} and life times ^{[clarification needed]} are not.^{[citation needed]} Brightness comparisons are also generally favorable.^{[clarification needed][citation needed]}

Other commercial product lines provide alternatives to individual members of the line of Alexa Fluor Dyes.^{[citation needed]} Comparisons with other dyes are less consistent,^{[clarification needed]} and also even more "delicate",^{[clarification needed]} depending on the conditions and techniques used.^{[editorializing][citation needed]} Such comparisons should be considered, depending on the conditions and techniques used, and the dye performance (signal, background, stability) needed.^{[editorializing][citation needed]}

• NCBI Staff (2013). Molecular Imaging and Contrast Agent Database (MICAD), 2004-2013. Bethesda, MD. PMID 20641179. Retrieved 1 March 2020.{{cite book}}: CS1 maint: location missing publisher (link) Database entries written by independent experts, on Alexa Fluor product numbers 488, 647, 680, 700, and 750, as well as other conjugated forms.
• Hullin-Matsuda F.; Murate M.; Kobayashi T. (25 September 2018). "Protein Probes to Visualize Sphingomyelin and Ceramide Phosphoethanolamine". Chem. Phys. Lipids. 216: 132–141. doi:10.1016/j.chemphyslip.2018.09.002. PMID 30194925. S2CID 52179117. Review of a lipid visualization application of the Alexa Fluors.
• Kozma, E.; Jayasekara, P.S.; Squarcialupi, L.; Paoletta, S.; Moro, S.; Federico, S.; Spalluto, G.; Jacobson, K.A. (1 January 2013). "Fluorescent Ligands for Adenosine Receptors". Bioorg. Med. Chem. Lett. 23 (1): 26–36. doi:10.1016/j.bmcl.2012.10.112. PMC 3557833. PMID 23200243. Review of a set of fluors based on Alexa Fluor (AF) 488, for receptor binding studies. Article presents structures of AF488 and AF532, as well as a large set of other standard flurophores Cy5, Texas Red, EVOBlue, FITC, NBD, Dansyl, 1-Pyrene, and various Bodipy complexes.