ライフサイエンスコーパス: cyanine dye

1 s conjugated to Cy5.5, a near-infrared (NIR) cyanine dye.

2 um, including a near-infrared (NIR)-emitting cyanine dye.

3 ine kinase c-Met conjugated to a fluorescent cyanine dye.

4 d to adjust the extent of aggregation of the cyanine dye.

5 model the trans-cis isomerization of a model cyanine dye.

6 plays an induction period unlike that of the cyanine dye.

7 PAINT) based on fluorogenic dimers of bright cyanine dyes.

8 t form covalent bonds with chloro-containing cyanine dyes.

9 and higher emission rates than commonly used cyanine dyes.

10 ic ligands, were prepared using red-emitting cyanine dyes.

11 d by PCR, and the products were labeled with cyanine dyes.

12 -helix DNA-binding motifs with intercalating cyanine dyes.

13 Herein we utilize cyanine dye 3,3'-diethyl-9-methyl-thiacarbocyanine iodid

14 tact and were detected using the symmetrical cyanine dye 3,3'-diethylthiadicarbocyanine iodide (DiSC2

15 erated photobleaching of the light-sensitive cyanine dye, 3,3'-diethylthiacarbocyanine iodide (DiSC(2

16 n-CsPb(Cl(0.7)Br(0.3))(3) nanocrystals and a cyanine dye (4,5-benzoindotricarbocyanine) show the part

17 engineering strategies designed to red-shift cyanine dye absorptions and emissions further into the n

18 ansferred through an acetylene bridge to the cyanine dye acceptor, which emits light at approximately

19 tion of densely packed, discrete clusters of cyanine dye aggregates with tunable absorption spectra a

20 Among those heptamethine cyanine dyes analyzed, 13 compounds within the nontoxic

21 tilized coupling between a tetrazine-derived cyanine dye and a trans-cyclooctene-modified bisphosphon

22 Pyrvinium is a quinoline-derived cyanine dye and an approved anti-helminthic drug reporte

23 ormation of an encounter complex between the cyanine dye and ionized thiol prior to their conjugation

24 to study the interaction between a cationic cyanine dye and peptide nucleic acid (PNA)-DNA duplexes.

25 e-shell nanoparticles that encapsulated with cyanine dyes and applied the dye-doped nanoparticles as

26 experiments compared a shielded heptamethine cyanine dye (and several peptide and antibody bioconjuga

27 re examined: Rhodamine 6G, crystal violet, a cyanine dye, and a cationic donor-acceptor substituted s

28 enching of a conjugated polyelectrolyte by a cyanine dye are investigated by femtosecond fluorescence

29 Cyanine dyes are a class of organic, usually cationic mo

30 Cyanine dyes are exceptionally useful probes for a range

31 Polymethine cyanine dyes are fascinating molecular wires because up

32 ocavities containing two spatially separated cyanine dyes are presented here, where simultaneous stro

33 Cyanine dyes are widely used fluorophores with a range o

34 Cyanine dyes are widely used in bioimaging, sensing, opt

35 Unsymmetrical cyanine dyes are widely used in biomolecular detection d

36 his is the first demonstration of an encoded cyanine dye as a ncAA in a eukaryotic expression system

37 at combines a rhodium metalloinsertor with a cyanine dye as the fluorescent reporter.

38 ntum dot-quantum rods (QD-QRs) as donors and cyanine dyes as acceptors, which are conjugated to QD-QR

39 terature survey indicated no previous use of cyanine dyes as contrast agents for in vivo optical dete

40 ed for the site-specific genetic encoding of cyanine dyes as non-canonical amino acids (Cy-ncAAs) int

41 Previous studies have utilized cyanine dyes as Tau aggregation inhibitors in vitro.

42 -to-high-yielding synthesis of unsymmetrical cyanine dyes bearing -COOH substituents for functionaliz

43 phile that initiates chain shortening of the cyanine dyes by attack on their polymethine backbones.

44 tion of a newly designed series of cationic, cyanine dyes by cucurbit[7]uril (CB7) can be used to alt

45 ble-walled nanotubes (DWNTs) formed from the cyanine dye C8S3 provide a robust, self-assembled system

46 esting nanotubes derived from an amphiphilic cyanine dye (C8S3-Cl).

47 Overall, a cyanine dye can dissociate aggregated Tau in an ex vivo

48 ation of albumin mutants and clinically-used cyanine dyes can help widen the clinical application pro

49 Five new cyanine dye cassettes were created by covalently attachi

50 d with increasing DS (of CMA), rendering the cyanine dye/CMA complex a more rigid (a high fluorescenc

51 Solution and solid-phase syntheses of a cyanine dye conjugated to polystyrene beads (desired for

52 , monofunctional, water-soluble heptamethine cyanine dyes containing a robust C-C bond at the central

53 dure to the synthesis of otherwise difficult cyanine dyes containing multiple heteroatoms in the indo

54 The cyanine dye Cy3 is a popular fluorophore used to probe t

55 or, for popular alkyl-thiols, are limited to cyanine dye Cy3 protection.

56 We report that the cyanine dye Cy5 and several of its structural relatives

57 BLM, deglycoBLM, and BLM disaccharide to the cyanine dye Cy5**.

58 assay, and in vivo optical imaging using the cyanine dye Cy5.5 conjugate.

59 n allowed the conjugation with a fluorescent cyanine dye (Cy5) and biotin, resulting in binding K(i)

60 blueing" reaction, in which the heptamethine cyanine dye Cy7 (IUPAC: 1,3,3-trimethyl-2-((1E,3E,5E)-7-

61 probe (TRAP) consisting of a monosubstituted cyanine dye derivatized with arsenic (i.e., TRAP_Cy3) to

62 lipid-specific since inclusion of a cationic cyanine dye, DiIC18(3), to impart positive charge in pla

63 layed library for binding to the fluorogenic cyanine dye Dimethyl Indole Red (DIR).

64 amer selected for binding to the fluorogenic cyanine dye, dimethylindole red (DIR), also binds and ac

65 Similar cyanine dyes (DiSC(3)(3), DiSC(4)(3), DiSC(5)(3), and Di

66 a rational approach to develop colorimetric cyanine dye-displacement assays that can be broadly appl

67 Other cyanine dyes (e.g., Cy3, Alexa 555) were not significant

68 data that show susceptibility of a class of cyanine dyes (e.g., Cy5, Alexa 647) to ozone levels as l

69 Heptamethine cyanine dyes enable deep tissue fluorescence imaging in

70 We have used a cyanine dye family as a paradigm and high-resolution cap

71 ry oligonucleotides were conjugated with the cyanine dye fluorophores Cy3 and Cy5 to quantify the mel

72 utility of the fluorous soluble pentamethine cyanine dye for tracking the localization of perfluoroca

73 evelop near-infrared fluorescent polymethine cyanine dyes for biological imaging and sensing.

74 library of near-infrared (NIR) heptamethine cyanine dyes for biomedical application as photoacoustic

75 ans of Stark effect in planar heterojunction cyanine dye/fullerene organic solar cells enables one to

76 A new asymmetric, squarylium cyanine dye functionalized by boronic acid ("SQ-BA") was

77 -infrared window of fluorescent heptamethine cyanine dyes greatly facilitates biological imaging beca

78 d the photophysics of the series and monomer cyanine dye have been studied in solution.

79 Cyanine dyes have been shown to undergo reversible photo

80 Polymethine cyanine dyes have been widely recognized as promising ch

81 lass of NIR fluorescent dyes, pyrrolopyrrole cyanine dyes, have exceptionally long FLTs ranging from

82 and MeHg(+) -responsive near-infrared (NIR) cyanine dye (hCy7) for MeHg(+) detection within living s

83 spectroscopy, and DFT modeling on a range of cyanine dyes, herein we show that photoinduced electron

84 -rotaxane supramolecular assembly with a Cy7 cyanine dye (hexamethylindotricarbocyanine) threaded alo

85 all the dyes studied relative to a benchmark cyanine dye (ICG) during photoexcitation with exceptiona

86 ons from PbS QDs by adsorbed J-aggregates of cyanine dye in aqueous dispersions.

87 is observed from J-aggregates of the achiral cyanine dye in association with a random coil CMA, sugge

88 l trimethine, pentamethine, and heptamethine cyanine dyes in near-quantitative yields.

89 el doubly strapped zwitterionic heptamethine cyanine dyes, including a structural analogue of ZW800-1

90 ing long-standing challenges associated with cyanine dyes, including undesired cis-trans photoisomeri

91 nding of structure-property relationships in cyanine dyes is critical for their design and applicatio

92 oping structure-aggregation relationships of cyanine dyes is crucial for controlling their optical pr

93 The benzothiazole cyanine dye K21 forms dye aggregates on double-stranded

94 irect the formation of dye aggregates with a cyanine dye, K21, into discrete branched photonic comple

95 Here, we show that, when cyanine-dye labeled 2'-deoxy and 2'-O-methyl oligonucleo

96 Receptor-bound, cyanine dye-labeled ligands, [Cy]ligands, were discrimin

97 s employed using an "always-ON" heptamethine cyanine dye (lambda(ex) = 785 nm) and the pH-responsive

98 Although cyanine dye loading is often accompanied by fluorescence

99 Polymethine bridges in cyanine dyes may be constrained by setting them into edg

100 's complexity: cylinders self-assembled from cyanine-dye molecules.

101 are resolved by employing a NIR heptamethine cyanine dye named s775z whose chemical structure is very

102 spectral properties of a series of dianionic cyanine dyes of the rare A(1)-n-A-n-A(1) type, with the

103 ese studies demonstrate that the red-shifted cyanine dyes offer spectral flexibility in multiplexed i

104 scission by a single photon ever observed in cyanine dyes or at wavelengths exceeding 800 nm.

105 estigated for polyelectrolytes consisting of cyanine dye pendant polylysines ranging in number of pol

106 Cyanine dyes play an indispensable and central role in m

107 The influence of the DNA target and probe cyanine dye position on oligo-DNA duplex formation behav

108 The binding interactions between two cyanine dyes, pseudoisocyanine (PIC) and pinacyanol (PIN

109 were obtained for host-guest films using two cyanine dyes, reaching 27%.

110 water solubility by modifying rhodamine and cyanine dye scaffolds with multiple sulfonate groups.

111 we have introduced the bis-quinoline (BisQ) cyanine dye that emits light in the red region (605-610

112 YTOX Green stain is a cationic unsymmetrical cyanine dye that is excluded from live cells but can rea

113 We have developed a new unsymmetrical cyanine dye that overcomes this problem.

114 Here, we introduce fluorous cyanine dyes that represent the most red-shifted fluorou

115 the corresponding electronic potential makes cyanine dyes the compounds to which simple free-electron

116 g is first visualized through conjugation of cyanine dyes, then biological utility is highlighted by

117 The cyanine dye thiazole orange (TO) is a well-known fluorog

118 s efficient energy transfer from the central cyanine dye to the surrounding zinc porphyrin nanoring.

119 le fragment antibody protein and a family of cyanine dyes to create new protein-dye fluoromodules tha

120 beling methodology that uses platinum-linked cyanine dyes to directly chemically label mRNA from as l

121 nsfers the pH sensitivity of photolabile NIR cyanine dyes to highly emissive and long-lifetime pH-ins

122 y attaching cyanine 7 (Cy7), a near-infrared cyanine dye, to tilmanocept, a radiopharmaceutical that

123 the direct transformation of Zincke salts to cyanine dyes under mild conditions, accompanied by the i

124 amplified quenching of PPESO3 by a series of cyanine dyes via singlet-singlet energy transfer.

125 A symmetrical cyanine dye was previously shown to bind as a cofacial d

126 phenyl-, and phenyl-substituted heptamethine cyanine dyes were prepared by a modified Suzuki--Miyaura

127 is study, four novel pentamethine indolizine cyanine dyes were synthesized with N,N-dimethylaniline-b

128 Therefore, the heptamethine cyanine dye will be an attractive scaffold to create a s

129 sensor 790 combines a near-infrared emitting cyanine dye with a sulfur-rich receptor to provide a sel

130 on between DNA and a benzothiazole-quinoline cyanine dye with a trimethine bridge (TO-PRO-3) results

131 marin, fluorescein, BODIPY, rhodamine B, and cyanine dyes with a photochemically active aryl azide gr

132 h high affinity to several other fluorogenic cyanine dyes with emission wavelengths covering most of

133 In recent work to develop cyanine dyes with especially large Stokes shifts, we enc

134 In water, cyanine dyes with extended conjugation are known to cros

135 ssisted synthesis of asymmetric pentamethine cyanine dyes with various functional groups was develope

136 ionships are explored for the six indolizine-cyanine dyes with varying cyanine bridge length and indo

137 labeling method using ISEL combined with the cyanine dye YOYO-1 that binds to DNA.