ライフサイエンスコーパス: nonfluorescent

1 er reduced to hydroresorufin (uncoloured and nonfluorescent).

2 self-pollination, the ddm1/ddm1 lines became nonfluorescent.

3 rescent proteins and thus render macrophages nonfluorescent.

4 idase to selectively render unesterified DHE nonfluorescent.

5 ith an aldehyde group to render the molecule nonfluorescent.

6 luorescence assay, based on the oxidation of nonfluorescent 10-acetyl-3,7-dihydroxyphenoxazine (Ample

7 rs to form upon oxidative cyclization of the nonfluorescent 2:1 lysine-HNE Michael adduct-Schiff base

8 , 151, 160 167, 188, and 210 of cTnI and the nonfluorescent acceptor 4-(dimethylamino)phenylazophenyl

9 Using a nonfluorescent acceptor eliminates the necessity to spec

10 les containing a C5-DMB-lipid are mixed with nonfluorescent acceptor vesicles.

11 h the fluorescent donor 1,5-IAEDANS, and the nonfluorescent acceptor, DAB-Mal.

12 eines were protected with the impermeant and nonfluorescent agent, methanethiosulfonate ethyltrimethy

13 de generated by pyruvate oxidase reacts with nonfluorescent Amplex Red at a 1:1 stoichiometry to form

14 Fluorescent markers and nonfluorescent analytes are initially mixed homogenously

15 ers of mobilities designed to bound those of nonfluorescent analytes of interest.

16 ytes can be used for detection of unlabeled (nonfluorescent) analytes.

17 orescence-activated cell sorting reverted to nonfluorescent and fluorescent phenotypes when placed in

18 that can be repeatedly photoswitched between nonfluorescent and fluorescent states, photobleaching li

19 Unbound dye is essentially nonfluorescent and has a large extinction coefficient (6

20 This species is nonfluorescent and has an absorbance maximum of 382 nm.

21 d were chosen so that the substrate would be nonfluorescent and the product fluorescent.

22 y blotting IEF was employed to monitor dark (nonfluorescent) and bright (fluorescent) GFP populations

23 ls, even when contaminating particles (i.e., nonfluorescent) are present.

24 d that the neutral lipid increased the total nonfluorescent area at surface pressures up to 25 mN/m b

25 the opposite effect of decreasing the total nonfluorescent area.

26 ve state, the reporter probe was essentially nonfluorescent at 700 nm due to energy resonance transfe

27 Here we describe a reversibly switchable nonfluorescent bacterial phytochrome for use in multisca

28 s a synthetic chymotrypsin substrate that is nonfluorescent before cleavage by chymotrypsin, but is i

29 These nonfluorescent benzofurazan sulfides react rapidly and s

30 resolution 3D images of both fluorescent and nonfluorescent biological specimens with a thickness of

31 eans to visualize the immobilization even of nonfluorescent biomolecules.

32 hich the tumors are first pretargeted with a nonfluorescent biotinylated monoclonal antibody [cetuxim

33 es turn into the emissive red phase from the nonfluorescent blue phase.

34 nit oxidized and the other reduced), and the nonfluorescent (both subunits reduced).

35 In aqueous solution, the probe is almost nonfluorescent but displays significant fluorescence enh

36 bution was found within the population, with nonfluorescent cells showing a much lower PCN (</=1) tha

37 two distinct subpopulations, fluorescent and nonfluorescent cells.

38 een prepared; in contrast to their virtually nonfluorescent character in most environments, the meroc

39 ed schemes can be used to indirectly measure nonfluorescent chemicals in microscopic domains.

40 Nonfluorescent chlorophyll catabolites (NCCs) were descr

41 escence, chlorophyll (Chl) is broken down to nonfluorescent chlorophyll catabolites (NCCs).

42 uorescent chlorophyll catabolites (FCCs) and nonfluorescent chlorophyll catabolites (NCCs).

43 nt to fluorescence microscopy for imaging of nonfluorescent chromophores and certain fluorophores.

44 This approach allows for the imaging of nonfluorescent chromophores and is generalizable to any

45 When the nonfluorescent chromoprotein asFP595 from Anemonia sulca

46 65 tripeptide, closely resembles that of the nonfluorescent chromoprotein Rtms5 in that the configura

47 The distinction between fluorescent and nonfluorescent colonies was exploited as a scorable phen

48 increases with increasing concentration of a nonfluorescent competitor ss DNA (d(T5-AT4AT5)) (C), ind

49 , the tetrapyrrole substrate, is a colorless nonfluorescent compound.

50 cin) and (ii) the ability to monitor cold or nonfluorescent compounds in a drug discovery setting.

51 ifferent analytes, including fluorescent and nonfluorescent compounds, with a variety of structures w

52 1 ratio between cis (fluorescent) and trans (nonfluorescent) conformations.

53 their specific interaction with Ac-Tempo, a nonfluorescent conjugate of fluorogenic acridine with pa

54 si disappeared abruptly at a transition to a nonfluorescent core continuous with the hair shaft.

55 FAs mimicked many properties of their native nonfluorescent counterparts, including uptake, distribut

56 while background cysteines are blocked with nonfluorescent covalent modifiers.

57 was prevented or reversed by addition of the nonfluorescent COX inhibitor (S)-flurbiprofen.

58 Subsequent click reactivity with nonfluorescent dansyl azide results in a 70-fold fluores

59 molecular constitution of the most abundant nonfluorescent DCC (NDCC), At-NDCC-1, was determined.

60 tion of Amplex Red, which is a colorless and nonfluorescent derivative of dihydroresorufin, produces

61 s: diazabenzoindoles, which remain virtually nonfluorescent, despite having a similar, rigid structur

62 ression of the different monolayers produced nonfluorescent domains that emerged for temperatures bet

63 nd repaired with grafts from strain-matched, nonfluorescent donors and secured in place with fibrin g

64 Continuous measurement of efflux of nonfluorescent drugs on the same cell culture in situ, o

65 ive cells and fluorescently stained by small nonfluorescent dye molecules added from outside the cell

66 We report here a novel, water-soluble, nonfluorescent dye that efficiently quenches fluorescenc

67 Specifically, a nonfluorescent dye, BCECF-AM, is able to penetrate both

68 ion in the presence of a strongly absorbing, nonfluorescent dye.

69 Dark fluorescence quenchers are nonfluorescent dyes that can modulate the fluorescence s

70 technique is extensible to a wide variety of nonfluorescent dyes.

71 een fluorescent protein from a background of nonfluorescent E. coli cells and shown that the bacteria

72 imental mixtures composed of fluorescent and nonfluorescent endocrine disruptors were analyzed.

73 mical assay format for the immobilization of nonfluorescent enzyme substrate, Leucine-GlutamicAcid-Hi

74 .8 microM) is comparable to that of cAMP and nonfluorescent Epac-selective agonist 8-(4-chlorophenylt

75 PvdP converts the nonfluorescent ferribactin, containing two iron binding

76 action within the material that converts the nonfluorescent film into a globally fluorescent material

77 ctural similarities between luciferase and a nonfluorescent flavoprotein, which is expressed in the l

78 In the second, caged (nonfluorescent) fluorescein-dextran was microinjected in

79 s article is to highlight the versatility of nonfluorescent Forster resonance energy transfer (FRET)

80 on, in which fluorescence is produced by two nonfluorescent fragments (N and C) of cyan fluorescent p

81 protein-fragment complementation, using two nonfluorescent fragments derived from fluorescent protei

82 ssay is based on the association between two nonfluorescent fragments of a fluorescent protein when t

83 Nonfluorescent fragments of the fluorescent protein Venu

84 is based on the complementation between two nonfluorescent fragments of the yellow fluorescent prote

85 ncorporation ratios (IRs=1.9 and 3.8) of the nonfluorescent FRET acceptor, K(D) values of 0.04+/-0.02

86 DNA sequencing analysis of nonfluorescent GFP clones indicated that the mutations i

87 ed on functional complementation between two nonfluorescent GFP fragments, can be used to detect the

88 extrinsic probe positions in the presence of nonfluorescent GM1.

89 Thus, formation of nonfluorescent ground-state hydrogen-bond complexes betw

90 Pc's possess a propensity to form nonfluorescent H-dimers that is utilized as the molecula

91 We prepared CHO cell lines expressing nonfluorescent halves (YN and YC) of yellow fluorescent

92 ugh a 1,2,3-triazole moiety, was essentially nonfluorescent in aqueous solutions.

93 he green fluorescent protein chromophore are nonfluorescent in solution but demonstrate a bright emis

94 pyr-1 diacetate (DA-ZP1-TPP), is essentially nonfluorescent in the metal-free state; however, exposur

95 The aldehydes are almost nonfluorescent in water, but addition of primary amines

96 ed by the activation illumination intensity; nonfluorescent inactive molecules are activated by a hig

97 he initial photochemical step, which forms a nonfluorescent intermediate absorbing at 696 nm (A696).

98 ther shows the antioxidant reactivity of the nonfluorescent intermediate semiquinone.

99 reaction, which can occur below 200 K, is a nonfluorescent intermediate with a broad absorbance band

100 e-resolved studies confirmed the presence of nonfluorescent intramolecular H-aggregates that increase

101 Nonfluorescent, ionic nanocrystals (NCs) of CdSe were co

102 Resazurin (blue and nonfluorescent) is reduced to resorufin (pink and highly

103 Determined pIC(50)s for nonfluorescent JNK-1 inhibitors were also consistent wit

104 pt study to apply SERS-based detection using nonfluorescent labels to investigate alternative gene sp

105 A four-plex detection scheme using nonfluorescent labels was demonstrated for DNA sequences

106 Nonfluorescent labels were used for an array-format mult

107 erved under most reaction conditions was the nonfluorescent lactam form of the originally fluorescent

108 itrogen atoms forces the molecule to adopt a nonfluorescent lactone form, providing a convenient meth

109 receptor-Gialpha2 fusion protein, and with a nonfluorescent ligand and receptor-GFP fusion protein.

110 saturation of the receptor binding site with nonfluorescent ligand and use of a null-reactive CCK rec

111 h either radiolabeled ligand binding assays (nonfluorescent ligands) or fluorescence intensity assays

112 Upon fusion of a nanodisc with a nonfluorescent liposome containing cognate proteins (for

113 fluorescent protein, and of fluorescent and nonfluorescent M3-M4 loops.

114 ple FRET (OS-FRET) method employing a novel, nonfluorescent methanethiosulfonate-linked acceptor that

115 Dihydroresorufin is a nonfluorescent molecule, which can be electrochemically

116 cence fluctuations, and when fluorescent and nonfluorescent molecules compete for surface binding sit

117 nsity, the concentrations of fluorescent and nonfluorescent molecules in solution, the solution diffu

118 tiate intramolecular cyclization and convert nonfluorescent molecules to highly fluorescent products.

119 iation rate constants of the fluorescent and nonfluorescent molecules, the surface site density, the

120 s can result in usefully high emission from "nonfluorescent" molecules and million-fold increases in

121 soluble peptides reacted slowly, generating nonfluorescent monooxygenated and dioxygenated products.

122 highly fluorescent photoproduct as well as a nonfluorescent monooxygenated photoproduct.

123 lyzed reaction between hydrogen peroxide and nonfluorescent N-acetyl-3,7-dihydroxyphenoxazine (Amplex

124 nd a photo-insensitive molecule (Amber) as a nonfluorescent (N) place holder: namely, NDAN, NDNA, and

125 luorescent NAD(P)H are assayed directly, and nonfluorescent NAD(P) are enzymatically reduced to their

126 The dye self-assembles to form nonfluorescent nanoparticles (Dh = 200 nm) which selecti

127 th affinity and specificity similar to their nonfluorescent natural counterparts.

128 We speculate that it is a nonfluorescent nonultraviolet active cross-link between

129 Photoactivation of nonfluorescent NQMP-caged 3-allyloxyfluorescein produces

130 he absolute binding density of the ligand on nonfluorescent nucleic acid is independent of a priori k

131 es between two different states, typically a nonfluorescent "off" state and a fluorescent "on" state

132 s present in the enzyme have been changed to nonfluorescent ones in various combinations without majo

133 have been performed because they either are nonfluorescent or lack an ionizable OH group.

134 hese amines and their imine derivatives were nonfluorescent or very weakly fluorescent.

135 tion of resazurin termed AlamarBlue from its nonfluorescent oxidized state to its fluorescent reduced

136 When the nonfluorescent peptide amphiphile component is designed

137 phile, and the second molecule is a shorter, nonfluorescent peptide amphiphile of complementary charg

138 e is hindered, and the compound remains as a nonfluorescent peptide conjugate.

139 ER delivery of a nonfluorescent peptide was demonstrated using a mAb high

140 te the NADH-driven oxidation of a colorless, nonfluorescent phenoxazine dye (Amplex Red) to a brightl

141 nedimethylimidazolinone (BDI) dye, is nearly nonfluorescent (Phif < 0.001) in common solutions at roo

142 rane organelles filled with melanin, a dark, nonfluorescent pigment.

143 FRET was diminished upon addition of nonfluorescent pre-SufI, indicating that the initial bin

144 ntails generating a fluorescent probe from a nonfluorescent precursor, 4-ethynyl-N-ethyl-1,8-naphthal

145 ifies structures labeled with fluorescent or nonfluorescent probes.

146 neous transformation of resorufin to less or nonfluorescent product(s) in the absence of hydrogen per

147 by metabolically active cells led to a final nonfluorescent product, and hence an underestimation of

148 sed on the chlorination of resorcinol to its nonfluorescent products in the presence of HOCl.

149 However, the flavin binding sites of the nonfluorescent protein are likely not representative of

150 We deduce the fraction of nonfluorescent proteins for EGFP, mRFP, and mCherry as w

151 159 and Cys171, locking the chromophore in a nonfluorescent protonated state.

152 cation and classification of fluorescent and nonfluorescent pseudomonads.

153 Here we report the use of a nonfluorescent quencher (Black Hole Quencher, BHQ) as an

154 rophore of the desired emission color, and a nonfluorescent quencher.

155 donor, and the beta-clamp was labeled with a nonfluorescent quencher.

156 Our results illustrate the potential of nonfluorescent quenchers in single-molecule correlation

157 d, 6-TAMRA) near the carboxyl terminus and a nonfluorescent quenching group (QSY-7) near the amino te

158 re and carries a 5'-fluorescent moiety, a 3'-nonfluorescent quenching moiety, and an appropriate clea

159 duct of the initial light-driven reaction, a nonfluorescent radical species, into a new intermediate

160 rface-enhanced Raman scattering (SERS) using nonfluorescent Raman labels to quantify gene expression

161 ntrolled through the surface coverage of the nonfluorescent Raman tags (RTags).

162 alently attach both DNA probing sequence and nonfluorescent Raman tags to the surface of gold nanopar

163 loyed for indirectly detecting absorbing but nonfluorescent reagents in microsamples, employing inner

164 a DMB, and (2) we monitored DMB delivery of nonfluorescent reagents into droplets preloaded with LY.

165 emission or absorption contrast, permitting nonfluorescent reporters for molecular imaging.

166 escent product resorufin at pH 7.0 or to the nonfluorescent resazurin at pH 4.0.

167 ons, and enzymatic oxidation of resorufin to nonfluorescent resazurin.

168 the beta-galactosidase-catalyzed reaction of nonfluorescent resorufin-beta-D-galactopyranoside to yie

169 -to-superficial pathway was not sensitive to nonfluorescent retrograde tracers including horseradish

170 Competitive binding experiments with nonfluorescent RNC species revealed that the nascent cha

171 ly accomplished with a long-term goal to use nonfluorescent RTags in a Raman-based DNA microarray pla

172 scherichia coli DnaB helicase to unmodified, nonfluorescent single-stranded nucleic acids where the i

173 For the DMPC/DSPC we found that the nonfluorescent solid regions gradually disappear in the

174 achieve separation and indirect detection of nonfluorescent species using fluorescent mobility marker

175 ethylrhodamines (AnMR) maintain a colorless, nonfluorescent spirocyclic structure at high pH.

176 ly high concentrations of Zn(ClO(4))(2), the nonfluorescent spirolactam component of 4 is transformed

177 d below the focal plane are transferred to a nonfluorescent state at each scanning step.

178 y between the half-fluorescent state and the nonfluorescent state.

179 reversibly converted between fluorescent and nonfluorescent states have proven to be a catalyst for i

180 n both the fluorescent and the light-induced nonfluorescent states reveal that the rapid and complete

181 stic, optical control of its fluorescent and nonfluorescent states, and subsequently applying a lock-

182 Two nonfluorescent states, D1 and D2, exist in a voltage-dep

183 by a highly selective thioether spirocyclic nonfluorescent structure that opens to form a mixture of

184 esults showed that nanoceria can oxidize the nonfluorescent substrate ampliflu, either to the very st

185 quenched in the protein, yielding virtually nonfluorescent substrate molecules.

186 ese results are applicable to natural (i.e., nonfluorescent) substrates.

187 The nonfluorescent terphenyl diazoketone 1 was transformed i

188 relies on the hematin-catalyzed oxidation of nonfluorescent thiamine to fluorescent thiochrome by H2O

189 ior exposure of cells to the impermeable and nonfluorescent thiol-specific agent ethyltrimethylammoni

190 "highlighters", which can be converted from nonfluorescent to fluorescent or from one color to anoth

191 se, primer extension by DNA polymerase using nonfluorescent TPLFNs generates fluorophores, which are

192 lemented with iron gave increased numbers of nonfluorescent trichomonads.

193 dy (MAb) to P270 yields both fluorescent and nonfluorescent trichomonads.

194 45 protein containing 4-fluorotryptophan, a nonfluorescent tryptophan analogue, subunit exchange bet

195 lysis of the PriA helicase interactions with nonfluorescent, unmodified nucleic acids has been perfor

196 lysis of the DnaB helicase interactions with nonfluorescent, unmodified nucleic acids has been perfor

197 signed small ligand is membrane-permeant and nonfluorescent until it binds with high affinity and spe

198 ped with rhodamine spirolactam dyes that are nonfluorescent until they encounter mercury ions, which

199 o3 or pyrene maleimide, that are essentially nonfluorescent until they react with a thiol.

200 was localized in the cytoplasm, whereas the nonfluorescent version was localized to the periplasmic

201 g vesicles were vastly outnumbered by older, nonfluorescent vesicles.

202 istic of an H-aggregate that was practically nonfluorescent, whereas in organic media, they displayed

203 ue-green region of the spectrum, while 4c is nonfluorescent, which is likely attributable to an intra

204 tion of Nef with a partner kinase juxtaposes nonfluorescent YFP fragments fused to the C terminus of

205 Cation exchange (CX) in the nonfluorescent ZnS nanocrystal clusters (NCCs) was emplo