ライフサイエンスコーパス: fluorescence microscopy

1 nalysis of emerging 3D in vitro models using fluorescence microscopy.

2 signaling molecules inside cells using basic fluorescence microscopy.

3 apping of concentration profiles by confocal fluorescence microscopy.

4 le to studying membrane traffic by live-cell fluorescence microscopy.

5 as assessed in a salivary rinse sample using fluorescence microscopy.

6 acizumab-800CW accumulation was evaluated by fluorescence microscopy.

7 context of the cell is a major challenge in fluorescence microscopy.

8 uring a potential scan using single-molecule fluorescence microscopy.

9 ce microscopy, and total internal reflection fluorescence microscopy.

10 l DNA binding proteins using single-molecule fluorescence microscopy.

11 membrane of living cells by single-molecule fluorescence microscopy.

12 correction of sCMOS-related noise (ACsN) for fluorescence microscopy.

13 r dSTRIDE), in nuclei of single cells, using fluorescence microscopy.

14 laser light scattering, SDS-PAGE and optical-fluorescence microscopy.

15 xts, complementing the prevailing volumetric fluorescence microscopy.

16 -sensitive fluorescence probes visualized by fluorescence microscopy.

17 y important tool for image reconstruction in fluorescence microscopy.

18 lls and airway macrophages was visualized by fluorescence microscopy.

19 shapes and observe the director field using fluorescence microscopy.

20 ent model; these results were confirmed with fluorescence microscopy.

21 mmunostaining, H&E staining, and light-sheet fluorescence microscopy.

22 and to be amenable to barium sensing through fluorescence microscopy.

23 using ethyl cinnamate (ECi) with light sheet fluorescence microscopy.

24 rypts which were assayed in situ by confocal fluorescence microscopy.

25 and pathologists experienced in conventional fluorescence microscopy.

26 oiling control with spatial manipulation and fluorescence microscopy.

27 nd in primary mouse and human hepatocytes by fluorescence microscopy.

28 e standard for those practising quantitative fluorescence microscopy.

29 location in gastric and intestinal cells by fluorescence microscopy.

30 o imaging of blood and lymphatic vessels via fluorescence microscopy.

31 inhibition with a fluorescent PA sensor and fluorescence microscopy.

32 oral organs of Arabidopsis using light sheet fluorescence microscopy.

33 ocusing that are associated with standard 3D fluorescence microscopy.

34 in with transmission electron microscopy and fluorescence microscopy.

35 in thiol (NPSH) imaging in lysosomes through fluorescence microscopy.

36 at the single-particle level using two-color fluorescence microscopy.

37 ication of nanographenes in super-resolution fluorescence microscopy.

38 w class of fluorophores for super-resolution fluorescence microscopy.

39 r wide-field, confocal, and super-resolution fluorescence microscopy.

40 gth scales are inaccessible with established fluorescence microscopy.

41 ultrasensitive ratiometric measurements and fluorescence microscopy.

42 thin the cell is measured, as in the case of fluorescence microscopy.

43 slets of BALB/c nude mice was examined using fluorescence microscopy.

44 ce (SPR), atomic force microscopy (AFM), and fluorescence microscopy.

45 ere examined using differential staining and fluorescence microscopy.

46 as tension) with single-cell O(2) saturation fluorescence microscopy.

47 ucture and fibrin formation were assessed by fluorescence microscopy.

48 tochondrial volume, as shown by quantitative fluorescence microscopy.

49 in real time with total internal reflection fluorescence microscopy.

50 in optical data storage and super-resolution fluorescence microscopies.

51 ces and enable new avenues for automation of fluorescence microscopy acquisition pipelines.

52 ions from purified nuclei, enzymatic assays, fluorescence microscopy, affinity chromatography, MS, an

53 Fluorescence microscopy allows identification of cellula

54 Further combination with fluorescence microscopy allows users to determine cells

55 Fluorescence microscopy also enables scientists and clin

56 velopment of single-molecule switching (SMS) fluorescence microscopy (also called single-molecule loc

57 ro for a defined period of time, imaged with fluorescence microscopy and analyzed with software that

58 tially correlated far-field super-resolution fluorescence microscopy and atomic force microscopy, a f

59 -based targeting is ideal for photon intense fluorescence microscopy and biological imaging.

60 for a wide range of applications in advanced fluorescence microscopy and biotechnology.

61 Combining single-molecule fluorescence microscopy and classic biochemical methods,

62 Superresolution fluorescence microscopy and cryogenic electron tomograph

63 Moreover, live light-sheet fluorescence microscopy and cultured PDGFRalpha+ cells r

64 brain tissue with one-photon and two-photon fluorescence microscopy and define the signal limits of

65 Using total internal reflection fluorescence microscopy and density gradient centrifugat

66 Here, we use a novel combination of X-ray fluorescence microscopy and depositional chronology in a

67 pled Cu(II) centres as evidenced by confocal fluorescence microscopy and electron paramagnetic resona

68 detected with steady-state and time-resolved fluorescence microscopy and flow cytometry (FCM).

69 om normal cells based on NQO1 activity using fluorescence microscopy and flow cytometry.

70 a technique that combines the advantages of fluorescence microscopy and flow cytometry.

71 Here, fluorescence microscopy and genetics were used to confir

72 tic combination of total internal reflection fluorescence microscopy and image correlation spectrosco

73 cells using light-sheet and micro-endoscopic fluorescence microscopy and imaging of retinal vasculatu

74 Fluorescence microscopy and immunoblot analyses were use

75 Using fluorescence microscopy and immunoblotting, we show here

76 EMI-137 binding specificity was assessed by fluorescence microscopy and in vitro experiments.

77 have become invaluable probes for multicolor fluorescence microscopy and in vivo imaging.

78 lysed on-chip at different time points using fluorescence microscopy and Lactate dehydrogenase (LDH)

79 droplet arrays by two complementary methods, fluorescence microscopy and mass spectrometry.

80 high-resolution mini-endoscopy, light-sheet fluorescence microscopy and micro-CT imaging in mice.

81 As visualized by X-ray fluorescence microscopy and nanoscale secondary ion MS (

82 Using fluorescence microscopy and quantitative image analysis

83 njunction with three-dimensional light-sheet fluorescence microscopy and single-cell RNA sequencing t

84 llenges for low-light applications common to fluorescence microscopy and single-molecule imaging.

85 Through fluorescence microscopy and spectroscopy as well as smal

86 Here, using super-resolution fluorescence microscopy and spectroscopy combined with b

87 Mating experiments, fluorescence microscopy and TEM revealed indigenous bact

88 The aim of this study was to apply fluorescence microscopy and the bacteria staining kit Li

89 hat enable the visualization of microbes via fluorescence microscopy and the non-destructive measurem

90 Fluorescence microscopy and time-resolved fluorescence s

91 In this study, the system utilizes fluorescence microscopy and unsupervised image analysis,

92 ted in multi-photon (two-photon) light-sheet fluorescence microscopy and, furthermore, can be achieve

93 le-molecule TIRFM (total internal reflection fluorescence microscopy) and developed a kinetic model t

94 5/175 [98-100%]) for smear-positive samples (fluorescence microscopy), and 81% (87/107 [73-88%]) in s

95 nation microscopy, total internal reflection fluorescence microscopy, and coimmunoprecipitation studi

96 X-ray micro-computed tomography (micro-CT), fluorescence microscopy, and fine root hydraulic conduct

97 Here, using human cell lines, fluorescence microscopy, and pulldown and immunoblotting

98 as semi-quantified by Live/Dead staining and fluorescence microscopy, and visualised by environmental

99 cence; confocal or total internal reflection fluorescence microscopy; and western blotting.

100 In this study, we applied a fluorescence microscopy approach coupled with transcript

101 Here we use in vitro single-molecule fluorescence microscopy approaches in a purified yeast S

102 and RNA localization provided by multicolor fluorescence microscopy are reviewed.

103 Employing fluorescence microscopy as the reference, we demonstrate

104 Using superresolution fluorescence microscopy as well as live cell and quantit

105 s with CHH and determine carbonyl content by fluorescence microscopy assay which correlates (R = 0.91

106 ion into a product is followed by time-lapse fluorescence microscopy at the single-cell level.

107 t-ELIP) using differential interference and fluorescence microscopy, attenuation spectroscopy, and e

108 Superresolution fluorescence microscopy based on covalent labeling highl

109 SCM), a technique that can be applied to all fluorescence microscopy-based equilibrium partition coef

110 Total internal reflection fluorescence microscopy-based single molecule studies co

111 We utilized total internal reflection fluorescence microscopy, bulk actin assays, and EM to in

112 classification and localization of cells in fluorescence microscopy by benchmarking four leading obj

113 Recent developments in fluorescence microscopy call for novel small-molecule-ba

114 Conventional fluorescence microscopy can only provide ~300 nm resolut

115 Fluorescence microscopy can provide extensive informatio

116 In vivo fluorescence microscopy can reveal cellular and subcellu

117 Microcontact printing, followed by fluorescence microscopy characterization were performed

118 talized in 50-pL droplets and analyzed using fluorescence microscopy combined with an immunoassay bas

119 Using light-sheet fluorescence microscopy combined with genetic lineage la

120 ophils and their activation processes, where fluorescence microscopy commonly used in biology is used

121 lecular modeling, surface plasmon resonance, fluorescence microscopy, competitive binding assays, and

122 sed high concentrations of PZP in vitro, and fluorescence microscopy confirmed the presence of PZP in

123 Fluorescence microscopy confirms that the endogenous and

124 in the pigeon lagena using synchrotron X-ray fluorescence microscopy coupled with the analysis of ser

125 Here we use live-cell single-molecule fluorescence microscopy, coupled with confocal and elect

126 We also briefly describe how to integrate fluorescence microscopy data for targeted milling and cr

127 etection and mother-daughters association in fluorescence microscopy data.

128 promising detection results for a variety of fluorescence microscopy datasets of different sources, i

129 itectural, and organoid-wide properties from fluorescence microscopy datasets.

130 ed in mice by (111)In gamma scintigraphy and fluorescence microscopy demonstrating the potential use

131 sing biochemistry, total internal reflection fluorescence microscopy, electron microscopy and cryo-el

132 ous modalities and scales (light microscopy, fluorescence microscopy, electron microscopy, secondary

133 As an integral part of modern cell biology, fluorescence microscopy enables quantification of the st

134 Fluorescence microscopy enables spatial and temporal mea

135 In parallel, we conducted fluorescence microscopy experiments to determine the ful

136 Fluorescence microscopy, flow cytometry, and PCR were pe

137 Using fluorescence microscopy, fluorescence spectroscopy, and

138 These advances extend the reach of fluorescence microscopy for monitoring fast processes in

139 and operationally difficult for analysis by fluorescence microscopy (>100 cells) or multiparameter f

140 Due to its specificity, fluorescence microscopy has become a quintessential imag

141 The impact of fluorescence microscopy has been limited by the difficul

142 Super-resolution fluorescence microscopy has enabled important breakthrou

143 t lack organelle-specific information, while fluorescence microscopy has provided the latter without

144 Advances in fluorescence microscopy have introduced new assays to qu

145 The MS image and the fluorescence microscopy image were fused to spatially co

146 The adjacent slices were used to obtain fluorescence microscopy images to locate amyloid plaques

147 nd low signal to background ratios (SBRs) in fluorescence microscopy images.

148 (brightness) in each pixel from a series of fluorescence microscopy images.

149 ombinantly expressed proteins, turbidimetry, fluorescence microscopy imaging, and fluorescence recove

150 by single-platelet total internal reflection fluorescence microscopy imaging.

151 cer detection and surgery, as well as NIR-II fluorescence microscopy imaging.

152 of the combined merits of flow cytometry and fluorescence microscopy, imaging flow cytometry (IFC) ha

153 l indicator during in vivo single-cell-level fluorescence microscopy in a bioelectrochemical reactor,

154 g pathway using quantitative single particle fluorescence microscopy in a reconstituted system.

155 )) on the single-particle level by two-color fluorescence microscopy in a time-resolved manner.

156 e ternary mixtures can be studied exploiting fluorescence microscopy in giant unilamellar vesicles, a

157 X-ray transmission tomography and hard X-ray fluorescence microscopy in situ, Fourier transform infra

158 Here, we used fluorescence microscopy in the unicellular alga Chlamydo

159 Using single-molecule fluorescence microscopy in vivo in sporulating cells and

160 Fluorescence microscopy, in particular immunofluorescenc

161 UV absorbance, circular dichroism and fluorescence microscopy indicated that the microfluidic

162 Super-resolution fluorescence microscopy is a powerful tool to visualize

163 Fluorescence microscopy is an essential tool for biologi

164 Live-cell fluorescence microscopy is broadly applied to study the

165 But the biochemical resolving power of fluorescence microscopy is not as well optimized as its

166 Among optical imaging techniques light sheet fluorescence microscopy is one of the most attractive fo

167 To this end, one of the primary tools in fluorescence microscopy is that of computational deconvo

168 Widefield fluorescence microscopy is used to monitor the spiking o

169 foci when immunocytochemistry coupled to 2D fluorescence microscopy is used.

170 s together with single DNA measurements with fluorescence microscopy, it becomes clear that SPD tends

171 It is verified by fluorescence microscopy, laser-scanning confocal microsc

172 nce spectroscopy and laser confocal scanning fluorescence microscopy (LCSM).

173 Xpert) or point-of-care light-emitting diode fluorescence microscopy (LED-FM) for individuals screeni

174 In the present study, using fluorescence microscopy, liposome sedimentation, differe

175 Light sheet fluorescence microscopy (LSFM) provides a rapid and comp

176 elle dynamics are challenging to detect with fluorescence microscopy, making it difficult to determin

177 s in cells is number and brightness (N&B), a fluorescence microscopy method that is capable of measur

178 ng-enabled super-resolution across different fluorescence microscopy modalities.

179 Fluorescence microscopy of bacteria challenged with two

180 s, by comparison with correlative two-photon fluorescence microscopy of DNA and mitochondria.

181 Using time-resolved fluorescence microscopy of individual synthetic vesicles

182 exon 1a for mitochondrial translocation, but fluorescence microscopy of MOCS1AB variants (types II an

183 mal as well as PSMA immunohistochemistry and fluorescence microscopy of organ cryosections (tumor, ki

184 A-DR and CD11b, Prussian blue iron staining, fluorescence microscopy of rhodamine, and imaging mass c

185 s, we developed light-sheet illumination for fluorescence microscopy of small coral colonies.

186 s by performing a propidium iodide assay and fluorescence microscopy of supported MRSA mimetic bilaye

187 p their individual energetic status based on fluorescence microscopy of their endogenous NADH.

188 cal microscopy and total internal reflection fluorescence microscopy on fixed specimens.

189 Spectrally resolved fluorescence microscopy on single block copolymerized or

190 Many implementations of light sheet fluorescence microscopy operate with a large chamber fil

191 maged in toto at single-cell resolution with fluorescence microscopy over a period of 1 to 2 weeks.

192 This imaging is achieved through fluorescence microscopy paired with spectral probes that

193 Single-molecule fluorescence microscopy provides the spatial and tempora

194 with confocal and total internal reflective fluorescence microscopy, respectively.

195 aring combined with confocal and light sheet fluorescence microscopy revealed distinct populations of

196 res and proximal single cells by light-sheet fluorescence microscopy revealed that individual B cells

197 Live-cell fluorescence microscopy revealed that the proteasome clu

198 Fluorescence microscopy revealed typical web-like struct

199 mics and used high-resolution and time-lapse fluorescence microscopy, revealing that mitochondrial le

200 Moreover, single molecule fluorescence microscopy reveals that DNA-bound XPA exhib

201 ity, and related artifacts continue to limit fluorescence microscopy's utility.

202 icroscopy, a feat only obtained until now by fluorescence microscopy set-ups with spatial resolution

203 Furthermore, confocal fluorescence microscopy showed altered localization of e

204 Single-molecule total internal reflection fluorescence microscopy showed CaMKII dissociation from

205 neoformans titan cell formation in vitro (i) Fluorescence microscopy showed normal human IgG and IgM

206 dies demonstrated membrane disruption, while fluorescence microscopy showed the formation of lipid ag

207 olecular biology, mammalian cell culture and fluorescence microscopy skills.

208 Traces from single-molecule fluorescence microscopy (SMFM) experiments exhibit photo

209 c profiling and information from genome-wide fluorescence microscopy studies in the budding yeast Sac

210 Fluorescence microscopy studies reveal that BOFP can eff

211 We present a superresolution fluorescence microscopy study of the long-term effects o

212 with confocal and total internal reflection fluorescence microscopy suggested that Amot's role in ac

213 Fluorescence microscopy suggested that the hypersegmente

214 effective augmented reality (AR) system for fluorescence microscopy systems using a display screen a

215 Fluorescence microscopy technique was used to confirm th

216 among others; consequently, several advanced fluorescence microscopy techniques have been developed t

217 More recent advances in fluorescence microscopy techniques have enabled increasi

218 Super-resolved fluorescence microscopy techniques have enabled substant

219 Here, we use quantitative fluorescence microscopy techniques in live budding yeast

220 ical differences not visible by conventional fluorescence microscopy techniques.

221 l and expansion microscopy, and quantitative fluorescence microscopy techniques: fluorescence recover

222 ning in vivo MRI and ex vivo high-resolution fluorescence microscopy that involves: (i) a method for

223 ess of HIV membrane fusion can be tracked by fluorescence microscopy, the 3D configuration of protein

224 Using cold-stages, microfluidics, and fluorescence microscopy, the activity of binary mixtures

225 hase coexistence is routinely possible using fluorescence microscopy, the three-phase region is more

226 maximizes the biochemical resolving power of fluorescence microscopy, thereby providing the means to

227 tomatic tracking of biopolymer networks from fluorescence microscopy time-lapse sequences facilitates

228 nd single-molecule total internal reflection fluorescence microscopy (TIRFm) showed that nascent ring

229 ecule techniques - ranging from electron and fluorescence microscopies to electrical and force spectr

230 We applied 2-photon laser scanning fluorescence microscopy to analyze spontaneous dynamic f

231 ings were also validated qualitatively using fluorescence microscopy to assess NF efficacy against la

232 tomography (microCT), light microscopy, and fluorescence microscopy to characterize the dynamics of

233 dates, we utilized total internal reflection fluorescence microscopy to demonstrate dynamic colocaliz

234 rial cell repair assays with single-molecule fluorescence microscopy to demonstrate that both a C-ter

235 ons to lipid-labeled target vesicles and use fluorescence microscopy to detect individual, pH-trigger

236 radial intensity measurements (NuRIM) using fluorescence microscopy to determine the average positio

237 We used multiwavelength single-molecule fluorescence microscopy to directly image and quantitate

238 tion have improved the spatial resolution of fluorescence microscopy to enable molecular resolution w

239 Here, we used epi-illumination fluorescence microscopy to estimate relative chlorophyll

240 he chytrid Spizellomyces punctatus, and used fluorescence microscopy to explore chytrid cell biology

241 In addition, we used time-lapse fluorescence microscopy to image dynamic type VI secreti

242 c ribbons, we used total internal reflection fluorescence microscopy to image synaptic vesicles and r

243 Here, we used genetics and single-molecule fluorescence microscopy to investigate whether RecF and

244 eaction Rate Constant (CRRC) uses time-lapse fluorescence microscopy to measure a rate constant of a

245 To examine these features, we use fluorescence microscopy to measure the oligomer stabilit

246 Here we use single-molecule fluorescence microscopy to observe individual RNAP molec

247 reatment, we used whole-cell patch-clamp and fluorescence microscopy to record spontaneous excitatory

248 For this, we used in vivo miniaturized fluorescence microscopy to reliably track responses of t

249 reening, oil and water phases were imaged by fluorescence microscopy to reveal the micro to macro sca

250 s for these features, we use single-molecule fluorescence microscopy to study the interaction between

251 bined optical diffraction tomography and epi-fluorescence microscopy to systematically quantify the m

252 Here we use total internal reflection fluorescence microscopy to visualize growth of individua

253 of FGFR and employ total internal reflection fluorescence microscopy to visualize individual KLA mole

254 Here, we utilize single molecule fluorescence microscopy to visualize the real-time searc

255 l-trap optical tweezers, in combination with fluorescence microscopy, to monitor nucleosome unwrappin

256 cence lifetime imaging or two-photon excited fluorescence microscopy, to which Nile Red has never bee

257 Real-time fluorescence microscopy together with macroscopic releas

258 m, we used long-term quantitative time-lapse fluorescence microscopy, transmission electron microscop

259 se applications of SWIR molecular probes for fluorescence microscopy using conjugates of antibodies,

260 ent is recorded by total internal reflection fluorescence microscopy utilizing the generated evanesce

261 cture, we developed a method that applied UV-fluorescence microscopy, video analysis, and highly auto

262 Biomolecules were fluorescently labeled, and fluorescence microscopy was employed to assess their ele

263 Total internal reflection fluorescence microscopy was performed on oligomers cleav

264 opamine was used as a functional monomer and fluorescence microscopy was used for detection.

265 Time-lapse fluorescence microscopy was used to assess changes in ke

266 In this work, X-ray fluorescence microscopy was used to measure diffusion co

267 Using time-lapse fluorescence microscopy we observed that symmetric cell

268 ng single molecule total internal reflection fluorescence microscopy we show that Wsp1 synergizes wit

269 Harnessing superresolution fluorescence microscopy, we demonstrate that Mic60, a su

270 on experiments and total internal reflection fluorescence microscopy, we demonstrate that the conserv

271 Using atomic force and fluorescence microscopy, we demonstrate that unlike DDR1

272 Using fluorescence microscopy, we detected NR in activated mac

273 By live-cell fluorescence microscopy, we directly observe the exocyto

274 Here, using single-molecule fluorescence microscopy, we follow assembly of the entir

275 With total internal reflection fluorescence microscopy, we found that secreted fibronec

276 ible technique and total internal reflection fluorescence microscopy, we further demonstrate that HSP

277 hermophoresis, and total internal reflection fluorescence microscopy, we identified the N-terminal, d

278 says, reporter gene expression, and confocal fluorescence microscopy, we investigated whether uric ac

279 Using high-resolution fluorescence microscopy, we observed lower Ubx concentra

280 Using microfluidics and fluorescence microscopy, we observed the binding of the

281 lity assays, LC3B immunoblots, and live-cell fluorescence microscopy, we report here that in the pres

282 Here, using super-resolution fluorescence microscopy, we report that Miro proteins fo

283 in-BRET sensors coupled with high-resolution fluorescence microscopy, we show that all AT1R variants

284 Applying hybrid photoacoustic and fluorescence microscopy, we simultaneously monitored neu

285 Using fluorescence microscopy, we visualize and quantify the r

286 eosarcoma) by alkaline phosphatase (ALP) and fluorescence microscopy were performed to comprehensivel

287 Flow cytometry and fluorescence microscopy were used to analyze hematopoiet

288 ere is a need to overcome the limitations of fluorescence microscopy, where added fluorophores can si

289 rt 3D TFM methods typically rely on confocal fluorescence microscopy, which can impose limitations on

290 anar geometry readily accessible by confocal fluorescence microscopy, which enabled us for the first

291 on in CG fusion in total internal reflection fluorescence microscopy, which was caused by a reduced n

292 a combined approach of single-metal-particle fluorescence microscopy with (1)H NMR spectroscopy, we h

293 By dual-color spinning disk fluorescence microscopy with a time resolution of ~20 ms

294 ct techniques of cryoelectron microscopy and fluorescence microscopy with techniques of NMR spectrosc

295 Probes (BAC One or BAC Two) and evaluated by fluorescence microscopy (without the need for sample was

296 performed elemental quanitification by X-ray fluorescence microscopy (XFM) on a small cohort (n = 32)

297 ation synchrotron light sources, where X-ray fluorescence microscopy (XFM) provides micron or submicr

298 h-affinity lanthanide ion binding, and X-ray fluorescence microscopy (XFM).

299 ted tomography (XCT), with synchrotron X-ray fluorescence microscopy (XRF) and X-ray absorption near-

300 Such measurements are possible using fluorescence microscopy yet challenging due to sample mo