ライフサイエンスコーパス: fluorescent label

1 a membrane/lipophilic probe and as a peptide fluorescent label.

2 cted by the presence and localization of the fluorescent label.

3 e-1,3,6-trisulfonic acid to add charge and a fluorescent label.

4 stability make pyrene excimer an attractive fluorescent label.

5 and TOPO-capped CdSe/CdS quantum dot as the fluorescent label.

6 ernal reference in the form of a nonreactive fluorescent label.

7 was probed simultaneously with only a single fluorescent label.

8 h high specificity that correlates well with fluorescent labels.

9 eshly excised human skin using two different fluorescent labels.

10 abel-free monitored instead of using several fluorescent labels.

11 ular morphological changes and intracellular fluorescent labels.

12 r of complementary hairpin oligomers bearing fluorescent labels.

13 beled with up to four spectrally overlapping fluorescent labels.

14 is especially critical when detecting single fluorescent labels.

15 of a wide range of commercial antibodies and fluorescent labels.

16 ement assay (UFIDA) with near-infrared (NIR) fluorescent labels.

17 nd in vivo without the use of any additional fluorescent labels.

18 or secondary labeling with relatively bulky fluorescent labels.

19 sphate and Ca(2+), or by the identity of the fluorescent labels.

20 ide substrates by attaching PEG moieties and fluorescent labels.

21 olic signatures without the use of exogenous fluorescent labels.

22 fluence depends sensitively on the charge of fluorescent labels.

23 tiplexed measurements can be performed using fluorescent labels.

24 d and visualized by click-chemistry-mediated fluorescent labeling.

25 we designed a DDR2 construct appropriate for fluorescent labeling.

26 l cord and peripheral nerve that requires no fluorescent labeling.

27 metry to study the degree and positioning of fluorescent labeling.

28 h of PC12 cells was analyzed using ELISA and fluorescent labeling.

29 al nanoparticles for magnetic extraction and fluorescent labeling.

30 n containing only HPDL cells as monitored by fluorescent labeling.

31 ic nerve paraffin sections were examined for fluorescent labeling.

32 hat are visualized as punctate structures by fluorescent labeling.

33 al data storage and switching and biological fluorescent labeling.

34 therefore eliminating the need for exogenous fluorescent labeling.

35 try and photophysics, or the requirement for fluorescent labeling.

36 ick reactivity of both congeners observed by fluorescent labeling.

37 V staining strategy, with the amine-reactive fluorescent label, 5-(and-6)-Carboxyfluorescein Diacetat

38 Fluorescent-labeled (68)Ga-tilmanocept allows for PET im

39 Glycans derivatized with negatively charged fluorescent label 8-aminopyrene-1,2,6-trisulfonate (APTS

40 tages: use of unlabeled protein to eliminate fluorescent labeling, ability for characterization of pr

41 e velocities and displacements of individual fluorescent-labeled actin segments, at varying times thr

42 ducing end of disaccharides with an aromatic fluorescent label affords stable derivatives with proper

43 Finally, we found that site-specific fluorescent labeling allows monitoring of the transient

44 bivalent Smac-based ligand (Smac-1) and its fluorescent labeled analogue (Smac-1F) and characterized

45 This gave a displacement peak for a NIR-fluorescent-labeled analogue of phenytoin that appeared

46 e-1,3,6-trisulfonic acid (APTS) to provide a fluorescent label and a triple-negative charge, separate

47 es, we show the successful introduction of a fluorescent label and biotin for detection or affinity e

48 uding, the delivery of reagents to cells for fluorescent labeling and cell-surface engineering, the f

49 N-acetylneuraminidase digestion, followed by fluorescent labeling and detection of quinoxalinone deri

50 synthetic system permits cell-type-specific fluorescent labeling and exogenous variation of the rela

51 Fluorescent labeling and immunostaining showed that VF n

52 Furthermore, we also used fluorescent labeling and inactivation correlation on EAA

53 ce poor settings by eliminating the need for fluorescent labeling and optical detection instrumentati

54 As a proof of concept, localized fluorescent labeling and pH changes were purposely intro

55 We first outline the fluorescent labeling and quantification of two common en

56 Fluorescent labeling and scanning electron microscopy (S

57 In vivo fluorescent labeling and subcellular fractionation revea

58 mplex co-culture environments often requires fluorescent labelling and significant light exposure tha

59 bel-induced aggregation and that BBL with no fluorescent labels and a longer N-terminal tail folds in

60 used alternative to signal amplification via fluorescent labels and enzymatic methods.

61 ribosomes must be specifically labeled with fluorescent labels and molecular handles.

62 The design of four new fluorinated biaryl fluorescent labels and their attachment to nucleosides a

63 enerate tumor-specific affinity ligands with fluorescent labels and/or azide modifications at high pu

64 uantitative study on the binding kinetics of fluorescent-labeled and un-labeled molecules (lectin pro

65 emical lysis, size exclusion chromatography, fluorescent labeling, and chip gel electrophoresis were

66 rcumvents the need for bisulfite conversion, fluorescent labeling, and PCR and could therefore prove

67 oes not require surface functionalization or fluorescent labels, and has the potential to serve as a

68 To determine utility of a panel of six fluorescent labeled antibodies as a diagnostic tool for

69 We created a fluorescent-labeled antibody that recognizes periostin a

70 target tumor with prototype-radiolabeled or fluorescent-labeled, antibody-appended CNT constructs wa

71 Fluorescent-labeled antigen experiments indicated that a

72 Fluorescent labels are commonly used in bioassays to enh

73 Fluorescent labels are widely employed in biomarker quan

74 increase in the polarization signal from the fluorescent label as it is drawn in toward the active si

75 Using a variety of intracellular fluorescent labels as well as negative staining experime

76 summarized, and the applications in redox or fluorescent labeling, as well as in bioconjugations and

77 Fluorescent labeling at position 14, 32, 49, or 85 did n

78 By comparison, fluorescent labeling at position 41 reduced the affinity

79 in high yield by hydrazinolysis, followed by fluorescent labeling at the reducing terminus and high-p

80 Dual fluorescent labels attached to sandwich ssDNA probes wer

81 have labeled the Cu-protein azurin with the fluorescent label ATTO 655-N-hydroxysuccinimide(NHS)-est

82 also tested on RAW macrophages by the use of fluorescent-labeled bacteria.

83 logical investigations, in which traditional fluorescent labels based on organic molecules fall short

84 We report a novel class of biofunctional fluorescent labels based on trapping of approximately 10

85 eal-time imaging in zebrafish displayed that fluorescent-labeled blood vessels showed enhanced intrat

86 We used parabiosis to introduce fluorescent-labeled bone marrow-derived cells to mice wi

87 h are detected by quenching of an N-terminal fluorescent label by contact with various amino acids, c

88 In agreement with this interpretation, a fluorescent-labeled C-16 fatty acid diffused laterally w

89 31,000 and Fungal 60,000) preparations using fluorescent-labelled casein, meat myofibrillar and conne

90 LSC populations were identified using fluorescent-labeled cell sorting and transplantation int

91 of the online FACS-Chip-LCMS workflow, 5000 fluorescent labeled cells were enriched from a 5% hetero

92 Studies with fluorescent-labeled cells revealed that the melanoma cel

93 scence microscopy by colocalization of green fluorescent labeled cholesterol-encapsulated NPs and ear

94 acted with glutathione-S-transferase and the fluorescent labeling compound monochlorobimane to form a

95 Using fluorescent labeling, confocal microscopy, and 3D recons

96 hod for sequencing DNA that does not require fluorescent labelling could reduce costs and increase se

97 By employing fluorescent-labeled cysteine mutations, we observe that

98 oE3 and apoE4 also inhibited the uptake of a fluorescent-labeled derivative of the peptide, suggestin

99 nsemble and single molecule assays employing fluorescent labeled derivatives of EF-Tu, tRNA, and the

100 As shown by differential staining using fluorescent-labeled dextrans, cell bodies of dorsal fin

101 scherichia coli to directly visualize single fluorescent labeled DNA polymerase I (Pol) and ligase (L

102 We measured the distance between fluorescent-labeled DNA loci of various interloci contou

103 ere studied by conventional cytogenetics and fluorescent-labeled DNA probes (fluorescence in situ hyb

104 wever, care must be taken to ensure that the fluorescent labels do not influence the system being pro

105 rom all these observations, we conclude that fluorescent labels do not perturb the thermodynamic prop

106 do not have the multiplexing capability that fluorescent labels do.

107 Fluorescent-labeled donor T cells were detected in CNS l

108 -Carboxy-X-Rhodamine, Succinimidyl Ester), a fluorescent labeling dye.

109 ectron cryotomography, mass spectrometry and fluorescent labelling dyes, here we show that some envir

110 pectrometry is a valuable tool for measuring fluorescent labeling efficiency and specificity.

111 diolabeled drug quantified bulk delivery and fluorescent label established penetration of drug over f

112 protein synthesis of modified (e.g. mutated, fluorescent-labeled) exogenous components (ribosomes, am

113 Uptake profile of fluorescent-labelled exosomes in epithelial cells was as

114 Fluorescent labeling experiments further suggest that th

115 porium OB3b was demonstrated by isotopic and fluorescent labeling experiments.

116 icroscopic phase separation is detectable by fluorescent labeling, followed by cooling of the membran

117 part needed charge for electrophoresis and a fluorescent label for detection.

118 quantum dots (QDs) and their application as fluorescent label for immunoassay.

119 on-enhanced spin sensors as well as improved fluorescent labeling for bioimaging could be envisioned.

120 able fluorophores, a shortage of photostable fluorescent labels for bacteria has limited its use in t

121 Such methods, however, usually rely on fluorescent labels for chemical targeting, which could p

122 The specifics of quantum dots use as fluorescent labels for continuous monitoring under const

123 ve alternative to existing nanoparticles and fluorescent labels for non-invasive targeted imaging of

124 l serve as a valuable reference for choosing fluorescent labels for single-molecule motility assays.

125 les multiplexing by incorporating orthogonal fluorescent labels for the simultaneous detection of dif

126 While methods that use fluorescent labels for visualizing printed arrays prior

127 proteins into chloroplasts, and that provide fluorescent labels for visualizing the resultant structu

128 Retrograde fluorescent labeling from the site of transection combin

129 Fluorescent labeling from viral replication is thereby r

130 By microscopic analysis of fluorescent-labeled GalR, a regulon-specific transcripti

131 The study shows that fluorescent labeling has a significant influence on the

132 arch, and in particular the use of molecular fluorescent labels, has allowed investigation of heterog

133 filaments by determining the orientation of fluorescent labels, however with a strong drawback: pola

134 Enhanced photostability of fluorescent labels (i.e., maximum emitted photons before

135 ation in 96-well plates, glycan release, and fluorescent labeling; (ii) quantitative HPLC analysis, i

136 4/80(+) cells) were characterized by in vivo fluorescent labeling, immunohistochemistry, fluorescence

137 ise measurement of the average location of a fluorescent label in a DNA layer relative to the surface

138 and excellent stability to function as a NIR fluorescent label in the early detection of tumors.

139 hydrogel degradation products containing the fluorescent label in the surrounding tissues revealed a

140 ght exposure), a very promising property for fluorescent labeling in biology.

141 Our work indicates that fluorescent labeling in general affects the binding beha

142 extraction microcolumns, the behavior of NIR fluorescent labels in a displacement format, and the ove

143 notags (MNTs) are a promising alternative to fluorescent labels in biomolecular detection assays, bec

144 ly on a powerful direct binding assay called fluorescent labels in kinases ('FLiK'), which enables a

145 Varying the position of the fluorescent labels in the Htt monomer with expanded 51Q

146 nanoparticles are potentially interesting as fluorescent labels in, for instance (single particle), i

147 c substrate (water), and without introducing fluorescent labels, in fact, without utilizing any elect

148 more proteins than previously possible with fluorescent labels, including surface markers, cytokines

149 caspase-1 was detected using FAM-YVAD-FMK, a fluorescent-labeled inhibitor of caspases (FLICA) specif

150 ized into the target cells and delivered the fluorescent label into the cell nuclei.

151 Incorporation of diffusible fluorescent labels into the viral membrane and the viral

152 eoxynucleotide 5'-tetraphosphates in which a fluorescent label is attached to the terminal phosphate

153 Fluorescent labeling is a mainstream technology for dete

154 Fluorescent labeling is widely used in biological and ch

155 e cell RNA imaging using genetically encoded fluorescent labels is an important tool for monitoring R

156 The precise determination of the position of fluorescent labels is essential for the quantitative stu

157 Ribosomes containing fluorescent-labeled L11 and tRNAs labeled with fluoropho

158 Here, we track single, fluorescent-labeled large DNA molecules (11, 115 kbp) di

159 Myocardial vascular density (fluorescent-labeled lectin perfusion and CD31 immunofluo

160 ird site which allowed for introduction of a fluorescent label (library of compounds 2) or an alkyne-

161 remity muscle with slice recordings from the fluorescent-labeled lumbar MN cell bodies to establish t

162 Human and murine DC rapidly captured fluorescent-labeled mannoprotein by a mannose receptor-m

163 owever, there is no electrical analogue to a fluorescent label, meaning that it is not possible to id

164 bination-mediated, noninvasive combinatorial fluorescent labeling method for embryonic lineage tracin

165 Here, we present a single RNA sensitive fluorescent labeling method which allows us to label and

166 bility to detect nitroaromatic analytes, the fluorescent-labeled MIP particles were tested for their

167 of this study, it can be concluded that the fluorescent-labeled MIP system is a feasible method for

168 e a co-localized brain-wide data set of both fluorescent-labelled neurons and counterstained cell bod

169 ted the basis for previous observations that fluorescent-labeled neuropeptide Y (NPY) is usually rele

170 e used a model of intradermal injection with fluorescent-labeled, nonviable larvae from the helminth

171 The inherent assumption is that the fluorescent label observed under LM colocalises well wit

172 photon uncaging with two-photon imaging of a fluorescent label of surface AMPA receptors to monitor i

173 Post-treatment fluorescent labeling of 1 observed by confocal fluoresce

174 Fluorescent labeling of biological RNA is complicated by

175 lving problems encountered in widely applied fluorescent labeling of biomolecules for studying life p

176 Multicolor fluorescent labeling of both intra- and extracellular st

177 Fluorescent labeling of budding yeast nucleoli with CDC1

178 Retrograde fluorescent labeling of dental primary afferent neurons

179 ents was visualized using sequential 3-color fluorescent labeling of filaments after mechanical shear

180 yR1 and RyR2 isoforms, we used site-directed fluorescent labeling of FKBP12.6, ligand binding measure

181 licability of CuAIAC was demonstrated by the fluorescent labeling of functionalized polystyrene and b

182 Post-treatment fluorescent labeling of functionalized Pt(II)-based agen

183 peracetylation by Gcn5, we used differential fluorescent labeling of histones to monitor acetylation

184 new study has combined video microscopy with fluorescent labeling of host and parasite membranes to f

185 s work enables the site-specific, live-cell, fluorescent labeling of intracellular proteins at high d

186 Kme3), CX4-ONBD, is used to direct selective fluorescent labeling of Kme3 histone peptides.

187 Fluorescent labeling of LIT HLN B cells before adoptive

188 roaches to assess cytosolic delivery rely on fluorescent labeling of macromolecules with an "always o

189 e use membrane tether formation coupled with fluorescent labeling of membrane components to examine t

190 Furthermore, a spatially controlled fluorescent labeling of microtubules in live CHO cells w

191 Several methods exist for fluorescent labeling of N-glycans and subsequent chromat

192 Fluorescent labeling of pairs of sites on VHL for fluore

193 rporation Mediated by Enzymes), a method for fluorescent labeling of peptide-fused recombinant protei

194 sion of the biarsenical-tetracysteine tag to fluorescent labeling of peptides and proteins in chemica

195 Furthermore, in situ fluorescent labeling of phagosomes indicated that PKC-be

196 alcitonin (sCT) demonstrates the utility for fluorescent labeling of polymers and proteins.

197 slow conformational changes were revealed by fluorescent labeling of position 202, elicited by a mutu

198 e as the green fluorescent protein, enabling fluorescent labeling of proteins in a reversible and spe

199 Site-specific fluorescent labeling of proteins in vivo remains one of

200 Site-specific fluorescent labeling of proteins inside live mammalian c

201 We used in situ fluorescent labeling of proteins tagged with a short tet

202 The first issue is fluorescent labeling of proteins.

203 say for measuring MshB activity requires the fluorescent labeling of reaction mixtures and subsequent

204 tech, a method employing PNGase F digestion, fluorescent labeling of released glycans, and analysis b

205 By site-directed fluorescent labeling of residues in the S3-S4 region and

206 Simultaneous PEGylation and fluorescent labeling of sCT is also demonstrated, using

207 mbined visualization of bile acid uptake and fluorescent labeling of several NTCP variants indicated

208 em for conditional genetic manipulation with fluorescent labeling of single neurons for imaging.

209 duction platform, 'MultiBacTAG', (i) for the fluorescent labeling of target proteins and biologics us

210 luorescence in a quantifiable manner and the fluorescent labeling of targeted transcripts.

211 Fluorescent labeling of the cysteines also indicated tha

212 argeted to the RyR2 cytoplasmic assembly via fluorescent labeling of the FKBP12.6 subunit.

213 After fluorescent labeling of the interacting partners and liv

214 amino acids into proteins and the specific, fluorescent labeling of the intracellular ultrastructure

215 Fluorescent labeling of the primer extension products wa

216 agent is known to interfere with subsequent fluorescent labeling of the solubilized proteins, the de

217 scription complexes by the incorporation and fluorescent labeling of the thymidine analog 5-ethynyl-2

218 sualization systems successfully achieve the fluorescent labeling of the viral envelope and proteins,

219 dies of microtubule dynamics tend to rely on fluorescent labeling of tubulin, with tracking accuracy

220 ), a surrogate for l-methionine, followed by fluorescent labelling of AHA-containing cellular protein

221 Fluorescent labelling of Nylon microfibers with Nile Red

222 ron cryotomography (ECT) and new methods for fluorescent labelling of peptidoglycan are allowing new

223 Cryotomography of purified sacculi and fluorescent labelling of PG in live cells confirmed that

224 Efficient fluorescent labelling of single and double-stranded DNA

225 Fluorescent labelling of this hexapeptide showed that it

226 ttle as 1 h without the use of antibodies or fluorescent labels of any kind.

227 However, non-specific multi-site fluorescent labeling often results in a loss of native s

228 The fluorescent-labeled oligosaccharide pool and fractions w

229 ne with fluorescence detection and require a fluorescent label on a smaller-sized binding partner.

230 target DNA strands to measure the impact of fluorescent labeling on duplex stability.

231 product and the subsequent immobilization of fluorescent labels on the microparticle surface.

232 clude sample preparation, surface chemistry, fluorescent labels, optimizing the enzyme-substrate syst

233 tion were obtained using virally transfected fluorescent labeling or by immunolabeling after fixation

234 Without the need for fluorescent labeling or Coulter counting, the white bloo

235 atistics to be generated without the need of fluorescent labels or other modification groups.

236 ithout any disturbances by molecular probes, fluorescent labels, or immobilization of molecules.

237 In case of fractional fluorescent labeling, our simulations predicted that the

238 Fluorescent labeled PAC were able to promote ExPEC agglu

239 We report single and double fluorescent-labeled PAC with one or two chlorine atoms d

240 nt of effect or tracking of (14)C-labeled or fluorescent-labeled paclitaxel.

241 d delivery (CED) using both radiolabeled and fluorescent-labeled particles.

242 Using fluorescent labels, PCNA is shown to increase the bindin

243 Fluorescent-labeled peanut and soy extracts were used to

244 site-specific modification of antibodies for fluorescent labeling, PEGylation, protein cross-linking,

245 human chorionic gonadotropin (hCG), by using fluorescent-labeled polyclonal antibodies.

246 s have created a pressing need for efficient fluorescent labeling procedures to visualize and detect

247 r low-noise real-time kinetic measurement of fluorescent-labeled protein binding.

248 asurements indicated that the transgenes for fluorescent-labeled proteins did not disrupt normal stom

249 CCK) pharmacophores that are connected via a fluorescent labeled, rationally designed synthetic linke

250 loured probes were obtained in a single tube fluorescent labelling reaction; and varying the ratios o

251 e spectrum, which is required by many common fluorescent labeling reagents.

252 h an optimized particle design and efficient fluorescent labeling scheme, we demonstrate subattomole

253 We have demonstrated that the choice of fluorescent label significantly affects the fractional c

254 The addition of the fluorescent label significantly stabilizes the DNA duple

255 Scanning fluorescent labeling sites throughout the domain showed

256 y and contralaterally using three retrograde fluorescent label solutions: Alexa Fluor 488 10,000 mw d

257 additional enzymatic signal amplification or fluorescent labeling steps.

258 we present fusion protein- and intein-based fluorescent labeling strategies that can probe Fe-S clus

259 Fluorescent labeling studies showed that the constituent

260 endent energy transfer processes between the fluorescent labels, such as cyan, yellow and monomeric r

261 le push-pull fluorogens which produce bright fluorescent labels suitable for single-molecule superres

262 To address this issue, we developed a fluorescent labeling technique based on the Cu(I)-cataly

263 Fluorescent labeling techniques have been widely used in

264 , fluorescence correlation spectroscopy, and fluorescent labeling techniques have enabled new experim

265 imit barrier, reliance of such techniques on fluorescent labeling technologies prohibits quantitative

266 strands differing only by the presence of a fluorescent label tethered to the 5' end of the solution

267 ical properties drive development and use of fluorescent labels that absorb and emit at longer wavele

268 al fluorescent properties and yielded stable fluorescent labels that could be easily activated and bi

269 Our system offers permanent fluorescent labels that reveal fine morphological detail

270 able to generate long overhangs suitable for fluorescent labeling through end-filling or other techni

271 roach that monitors the separation between a fluorescent-labeled TMS and fluorescent phospholipids di

272 highly specific genetic tag for attaching a fluorescent label to a protein of interest.

273 probes that contain both a radiotracer and a fluorescent label to allow for enhanced intraoperative d

274 olecule photobleaching and substoichiometric fluorescent labeling to determine the aggregation number

275 electrophysiology, immunohistochemistry, and fluorescent labeling to directly assess cholinergic syna

276 Here, we used sequence-specific fluorescent labeling to map the incorporation patterns o

277 We used the bleaching of the fluorescent labels to determine the number of active flu

278 cules, such as nucleic acids or proteins and fluorescent labels to identify the target(s) of interest

279 imaging often relies on synthetic or genetic fluorescent labels, to provide contrast which can be far

280 Furthermore, the fluorescent-labeled universal aptamer used in this syste

281 to undergo conformational change and release fluorescent label upon interaction with the flow of the

282 are typically attributed to the influence of fluorescent labels used in smFRET and to the impact of h

283 uncertainty of this approach is whether the fluorescent labels used in the system will survive expos

284 Toward this end, triple-fluorescent labeling using antisera raised against PVB a

285 elf-quenching of emission from surface-bound fluorescent label was deduced from the response kinetics

286 man serum using gold nanoclusters (AuNCs) as fluorescent label was developed.

287 An minor grove binding Eclipse probe with a fluorescent label was used for detection.

288 was used to compromise cell membranes, and a fluorescent label was used to monitor the extent, result

289 Fluorescent labeling was confirmed by fragmentation expe

290 er laser exposure, a circular area devoid of fluorescent labeling was observed, indicating disruption

291 nt assays, on-chip sample preparation (e.g., fluorescent labeling, washing) can be performed, as oppo

292 of Western blotting and sulfhydryl-directed fluorescent labeling, we found that two large regions of

293 Only minor differences in fluorescent-labelling were observed between the dividing

294 fortunately, this method inherently requires fluorescent labeling which has several drawbacks.

295 on the non-linear and stochastic response of fluorescent labels which can be toxic and interfere with

296 Fluorescent labeling with NBD-sphingolipids or immunosta

297 We demonstrate their selective fluorescent labeling with respect to the proteome of liv

298 ther our understanding of complex processes, fluorescent labeling with visible light fluorescent prot

299 is shows the 3D relative movement of the two fluorescent labels with an accuracy of 30 nm.

300 By determining the positions of the fluorescent labels with respect to the DNA backbone, the