Optical properties and application of a reactive and bioreducible thiol-containing tetramethylrhodamine dimer

Bioconjugate Chemistry

Volumn 20, Issue 3, 2009, Pages 476-480

  Christie, R James ^a   Tadiello, Constantino J ^a   Chamberlain, Lisa M ^a   Grainger, David W ^a,b  

^a Department of Environmental and Radiological Health Sciences   (United States)

^b UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FLUORESCENCE; MONOMERS; OPTICAL PROPERTIES; OXIDATION; PHOSPHORUS COMPOUNDS; SULFUR COMPOUNDS;

ABSORBANCE INTENSITY; CYSTAMINE; DIMER FORMATION; HYPSOCHROMIC SHIFTS; INTENSITY RATIO; MONOMER SPECIES; NONCOVALENT; OPTICAL APPLICATIONS; SPECTRAL PROPERTIES; SYNTHESISED;

DIMERS;

DIMER; FLUORESCENT DYE; MERCAPTAMINE; PHOSPHATE BUFFERED SALINE; POLYMER; POLY[N (2 HYDROXYPROPYL)METHACRYLAMIDE]; TETRAMETHYLRHODAMINE; THIOL; TRIS(2 CARBOXYETHYL)PHOSPHINE; RHODAMINE; THIOL DERIVATIVE;

ARTICLE; CELL LYSATE; CHEMICAL STRUCTURE; CONJUGATION; DISULFIDE BOND; ENDOCYTOSIS; FLUORESCENCE; FLUORESCENCE RESONANCE ENERGY TRANSFER; GEL PERMEATION CHROMATOGRAPHY; HALF LIFE TIME; MACROPHAGE; OXIDATION; QUANTUM YIELD; REDUCTION; SPECTROSCOPY; SYNTHESIS; ANIMAL; CELL LINE; CHEMISTRY; DIMERIZATION; OXIDATION REDUCTION REACTION; SPECTROFLUOROMETRY;

ANIMALS; CELL LINE; DIMERIZATION; FLUORESCENT DYES; OXIDATION-REDUCTION; RHODAMINES; SPECTROMETRY, FLUORESCENCE; SULFHYDRYL COMPOUNDS;

EID: 63749128028     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc800367e     Document Type: Article

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