DY-635

Description

Fluorescent dye with absorbance max at 647 nm and emission max at 671 nm (measured in ethanol) from Dyomics GmbH (Jena, Germany). The DY-635 fluorescent dye is soluble in methanol, ethanol, DMF, DMSO.

The available modifications for this dye are carboxylic acid, NHS-ester, amino-derivative, maleimide, azide, phalloidin, and dUTP

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Nakamura M., Shono M., Ishimura K., Synthesis, Characterization, and Biological Applications of Multifluorescent Silica Nanoparticles, Anal. Chem., 79(2007)6507-6514.

Luschtinetz F., Dosche C., Kumke M. U., Influence of Streptavidin on the Absorption and Fluorescence Properties of Cyanine Dyes, Bioconjugate Chem., 20(2009)576-582.

Dietz L., Bosque A., Pankert P., Ohnesorge S., Merz P., Anel A., Schnölzer M., Thiers H.-J., Quantitative DY-maleimide-based proteomic 2-DE-labeling strategies using human skin proteins, PROTEOMICS, 9(2009)4298-4308

Schneider E.,  Keller M., Brennauer A., Hoefelschweiger B. K., Gross D., Wolfbeis O. S., Bernhardt G., Buschauer A., Synthesis and Characterization of the First Fluorescent Nonpeptide NPY Y1 Receptor Antagonist, ChemBioChem, 8(2007)1981-1988.

Schneider E., Mayer M., Ziemek R., Li L., Hutzler C., Bernhardt G., Buschauer A., A Simple and Powerful Flow Cytometric Method for the Simultaneous Determination of Multiple Parameters at G Protein-Coupled Receptor Subtypes, ChemBioChem, 7(2006)1400-1409

Keller M., Bernhardt G., Buschauer A., [3H]UR-MK136: A Highly Potent and Selective Radioligand for Neuropeptide Y Y1 Receptors, ChemMedChem 6(2011)1566-1571.

Pluym N.,  Baumeister P., Keller M., Bernhardt G., Buschauer A., [3H]UR-PLN196: A Selective Nonpeptide Radioligand and Insurmountable Antagonist for the Neuropeptide Y Y2 Receptor, ChemMedChem, 8(2013)587-593.

Napp J., Behnke T., Fischer L., Würth C., Wottawa M., Katschinski D. M.,  Alves F., Resch-Genger U.,  Schäferling M., Targeted Luminescent Near-Infrared Polymer-Nanoprobes for In Vivo Imaging of Tumor Hypoxia, Anal. Chem., 83(2011)9039-9046.

Szent-Gyorgyi C., Schmidt B. F., Fitzpatrick J. A. J., Bruchez M. P., Fluorogenic Dendrons with Multiple Donor Chromophores as Bright Genetically Targeted and Activated Probes, J. AM. CHEM. SOC. 132(2010)11103-11109.

Keller M., Pop N., Hutzler C., Beck-Sickinger A. G., Bernhardt G., Buschauer A., Guanidine-Acylguanidine Bioisosteric Approach in the Design of Radioligands: Synthesis of a Tritium-Labeled NG-Propionylargininamide ([3H]-UR-MK114) as a Highly Potent and Selective Neuropeptide Y Y1 Receptor Antagonist, J. Med. Chem., 51(2008)8168-8172.

Petty J. T., Fan C., Story S. P., Sengupta B., Iyer A. St. J., Prudowsky Z., Dickson R. M., DNA Encapsulation of Ten Silver Atoms Produces a Bright, Modulatable, Near Infrared-Emitting Cluster, J. Phys. Chem. Lett., 1(2010)2524-2529.

Soto C. M., Blum A. S., Vora G. J., Lebedev N., Meador C. E., Won A. P., Chatterji A., Johnson J. E., Ratna B. R., Fluorescent Signal Amplification of Carbocyanine Dyes Using Engineered Viral Nanoparticles, J. Am. Chem. Soc., 128(2006)5184-5189.

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