ライフサイエンスコーパス: cyanine dye

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

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

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

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

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

6 and higher emission rates than commonly used cyanine dyes.

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

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

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

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

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

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

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

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

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

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

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

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

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

20 Unsymmetrical cyanine dyes are widely used in biomolecular detection d

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

48 Cyanine dyes have been shown to undergo reversible photo

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

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

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

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

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

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

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

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

57 Although cyanine dye loading is often accompanied by fluorescence

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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