Literature DB >> 2917470

Cyanine dye labeling reagents containing isothiocyanate groups.

R B Mujumdar1, L A Ernst, S R Mujumdar, A S Waggoner.   

Abstract

New isothiocyanate derivatives of cyanine dyes were synthesized as fluorescent covalent labeling reagents for proteins and other biomolecules. These dyes have maximum absorbance in the red and near infrared regions of the spectrum, have high extinction coefficients and have adequate quantum yields. Incorporating two alkyl sulfonate groups in the dye structures increases their water solubility, which is beneficial for labeling biological molecules in aqueous solution. Reactivities of proteins with these new cyanines are similar to their reactivities with fluorescein isothiocyanate. These new labeling reagents are complementary to the fluorescein and rhodamine reagents, expanding the possibilities of multicolor analyses. Sheep anti-mouse-IgG antibody was labeled with a pentamethine cyanine dye (CY5.8-ITC) and used with a fluoresceinated antibody as a second reagent for detecting human T-cell subsets by flow cytometry.

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Year:  1989        PMID: 2917470     DOI: 10.1002/cyto.990100104

Source DB:  PubMed          Journal:  Cytometry        ISSN: 0196-4763


  28 in total

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2.  Iterative data analysis is the key for exhaustive analysis of peptide mass fingerprints from proteins separated by two-dimensional electrophoresis.

Authors:  Frank Schmidt; Monika Schmid; Peter R Jungblut; Jens Mattow; Axel Facius; Klaus Peter Pleissner
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3.  Improved speciation characteristics of PEGylated indocyanine green-labeled Panitumumab: revisiting the solution and spectroscopic properties of a near-infrared emitting anti-HER1 antibody for optical imaging of cancer.

Authors:  Aaron Joseph L Villaraza; Diane E Milenic; Martin W Brechbiel
Journal:  Bioconjug Chem       Date:  2010-11-12       Impact factor: 4.774

4.  Novel, monomeric cyanine dyes as reporters for DNA helicase activity.

Authors:  Cuiling Xu; Mykhaylo Yu Losytskyy; Vladyslava B Kovalska; Dmytro V Kryvorotenko; Sergiy M Yarmoluk; Sarah McClelland; Piero R Bianco
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5.  New method for covalent fluorescent biomolecule labeling with hemicyanine dye.

Authors:  Olexander M Kostenko; Vladyslava B Kovalska; Kateryna D Volkova; Pavel Shaytanov; Igor O Kocheshev; Yuriy L Slominskiy; Irina V Pisareva; Sergiy M Yarmoluk
Journal:  J Fluoresc       Date:  2006-06-15       Impact factor: 2.217

6.  New fluorescent dyes in the red region for biodiagnostics.

Authors:  M Sauer; K T Han; R Müller; S Nord; A Schulz; S Seeger; J Wolfrum; J Arden-Jacob; G Deltau; N J Marx; C Zander; K H Drexhage
Journal:  J Fluoresc       Date:  1995-09       Impact factor: 2.217

Review 7.  The challenges of sequencing by synthesis.

Authors:  Carl W Fuller; Lyle R Middendorf; Steven A Benner; George M Church; Timothy Harris; Xiaohua Huang; Stevan B Jovanovich; John R Nelson; Jeffery A Schloss; David C Schwartz; Dmitri V Vezenov
Journal:  Nat Biotechnol       Date:  2009-11-06       Impact factor: 54.908

Review 8.  Cytochemical detection systems for in situ hybridization, and the combination with immunocytochemistry, 'who is still afraid of red, green and blue?'.

Authors:  E J Speel; F C Ramaekers; A H Hopman
Journal:  Histochem J       Date:  1995-11

9.  When one plus one does not equal two: fluorescence anisotropy in aggregates and multiply labeled proteins.

Authors:  Zahra Zolmajd-Haghighi; Quentin S Hanley
Journal:  Biophys J       Date:  2014-04-01       Impact factor: 4.033

10.  Twisted cyanines: a non-planar fluorogenic dye with superior photostability and its use in a protein-based fluoromodule.

Authors:  Nathaniel I Shank; Ha H Pham; Alan S Waggoner; Bruce A Armitage
Journal:  J Am Chem Soc       Date:  2012-12-20       Impact factor: 15.419

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