ライフサイエンスコーパス: fluorescence microscopy

1 luorescent probes, making them detectable by fluorescence microscopy.

2 traction and immunocytochemistry followed by fluorescence microscopy.

3 te responses are imaged by using multiphoton fluorescence microscopy.

4 peed range comparable to that of light-sheet fluorescence microscopy.

5 on path resembles properties of conventional fluorescence microscopy.

6 a popular commercial system using two-photon fluorescence microscopy.

7 not yet been systematically tried in modern fluorescence microscopy.

8 brane lipid domains using flow cytometry and fluorescence microscopy.

9 ome marker, by Western blotting and confocal fluorescence microscopy.

10 remains a limiting factor in superresolution fluorescence microscopy.

11 ay and examined by total internal reflection fluorescence microscopy.

12 ghost fibres were investigated by polarized fluorescence microscopy.

13 amage recognition step using single-molecule fluorescence microscopy.

14 conjunction with atomic force microscopy and fluorescence microscopy.

15 ADF using in vitro total internal reflection fluorescence microscopy.

16 talization, in situ allele-specific PCR, and fluorescence microscopy.

17 f immuno-magnetic aggregates is confirmed by fluorescence microscopy.

18 carotid plaques by immunohistochemistry and fluorescence microscopy.

19 t we directly observed using single-molecule fluorescence microscopy.

20 demonstrated by flow cytometry and confocal fluorescence microscopy.

21 s and imaging of tagged proteins by confocal fluorescence microscopy.

22 and electrostatic (carboxyl) moieties using fluorescence microscopy.

23 cific locations, unambiguously identified by fluorescence microscopy.

24 es that enable singe-molecule detection with fluorescence microscopy.

25 otostability, as detected by single molecule fluorescence microscopy.

26 FlicR1 can be easily imaged with wide-field fluorescence microscopy.

27 ions in single-molecule and super-resolution fluorescence microscopy.

28 re localized to the endoplasmic reticulum by fluorescence microscopy.

29 -tagged APOBEC3 proteins using single-virion fluorescence microscopy.

30 d, incubated with the probe and imaged using fluorescence microscopy.

31 H was further demonstrated in HepG2 cells by fluorescence microscopy.

32 mputed tomography (CT), autoradiography, and fluorescence microscopy.

33 taken up by cells and could be visualized by fluorescence microscopy.

34 the resulting molecular self-assembly using fluorescence microscopy.

35 ollowed by PBMC chemotaxis determination via fluorescence microscopy.

36 t are directly observable using standard epi-fluorescence microscopy.

37 iposomal drug carriers were quantified using fluorescence microscopy.

38 their subcellular location in the plastid by fluorescence microscopy.

39 rce, confocal, and total internal reflection fluorescence microscopy.

40 n and oxidation is imaged by single-particle fluorescence microscopy.

41 become inadequate for the new challenges of fluorescence microscopy.

42 rotocol for interfacing 3D-MTC with confocal fluorescence microscopy.

43 was measured with Western blot analysis and fluorescence microscopy.

44 helial F-actin was determined using confocal fluorescence microscopy.

45 th energy-dispersive X-ray spectroscopy, and fluorescence microscopy.

46 nanotube-modified electrode was confirmed by fluorescence microscopy.

47 and detection of all four individual NSPs by fluorescence microscopy, a feature never achieved in pre

48 Combined force and single molecule fluorescence microscopy allowed us to directly monitor t

49 Fluorescence microscopy analysis indicates that the DOX

50 Here we present a fluorescence microscopy analysis termed pCOMB (pair corr

51 -turnover imaging of a molecular catalyst by fluorescence microscopy and allows detection of individu

52 shed multiple particle types with multicolor fluorescence microscopy and automated image analysis sof

53 Total Internal Reflection Fluorescence microscopy and biotinylation assays showed

54 Advances in fluorescence microscopy and calcium sensitive dyes has l

55 Here, using fluorescence microscopy and chromosome conformation capt

56 Using fluorescence microscopy and cryo-electron tomography, we

57 Fluorescence microscopy and electrochemistry were employ

58 Using fluorescence microscopy and electron tomography, we find

59 We utilized fluorescence microscopy and enzyme-linked immunosorbent

60 Fluorescence microscopy and FE-SEM indicated simultaneou

61 The tracer was characterized by fluorescence microscopy and flow cytometry assays in BXP

62 omic force microscopy combined with confocal fluorescence microscopy and Fourier transform infrared s

63 In vivo imaging was complemented by ex vivo fluorescence microscopy and gamma-counting of harvested

64 Fluorescence microscopy and high performance liquid chro

65 The rapid development in fluorescence microscopy and imaging techniques has great

66 le-molecule assay based on optical tweezers, fluorescence microscopy and microfluidics that, in combi

67 Light-sheet fluorescence microscopy and optical projection tomograph

68 modules for light-emitting diode (LED)-based fluorescence microscopy and optogenetic stimulation as w

69 racellular traps (NETs) was determined using fluorescence microscopy and picogreen assay.

70 mutant clones in microbial populations using fluorescence microscopy and population sequencing.

71 induced mechanical stimulation with confocal fluorescence microscopy and provides an optional extensi

72 ents suitable for western blotting, confocal fluorescence microscopy and pull-down applications.

73 cycloaddition enabled both visualization by fluorescence microscopy and quantification by HPLC.

74 Fluorescence microscopy and quantitative reverse transcr

75 ual lysosomes using quantitative ratiometric fluorescence microscopy and report an unappreciated hete

76 With the combination of fluorescence microscopy and reversed buffer flow operati

77 combines polarized total internal reflection fluorescence microscopy and single-molecule localization

78 n live cells using total internal reflection fluorescence microscopy and single-molecule tracking.

79 Single-molecule super-resolution fluorescence microscopy and single-particle tracking are

80 his meshwork using live-cell superresolution fluorescence microscopy and spatio-temporal image correl

81 Using fluorescence microscopy and spectroscopy, and dynamic an

82 Using total internal reflection fluorescence microscopy and structure illumination micro

83 Fluorescence microscopy and subcellular fractionation me

84 istent with similar measurements by confocal fluorescence microscopy and subcellular fractionation of

85 Here, we use single-molecule fluorescence microscopy and three-dimensional quantitati

86 Hyperspectral confocal fluorescence microscopy and three-dimensional structured

87 nstrate widefield (field diameter = 200 mum) fluorescence microscopy and video imaging inside the rod

88 system using TIRF (total internal reflection fluorescence) microscopy and purified human transcriptio

89 A combination of genetics, fluorescence microscopy, and biochemistry reveals three

90 al targeting, we used quantitative live-cell fluorescence microscopy, and compared the effects of the

91 GAGs binding was examined by flow cytometry, fluorescence microscopy, and gel electrophoresis.

92 ticles (20-1000 mum) using the dye Nile red, fluorescence microscopy, and image analysis software.

93 , isothermal titration calorimetry, confocal fluorescence microscopy, and in vivo photoactivatable cr

94 Using a combination of proteome analysis, fluorescence microscopy, and membrane analysis we show t

95 us confocal reflectance microscopy, confocal fluorescence microscopy, and rheology.

96 cence confocal and total internal reflection fluorescence microscopy, and sliding window temporal ima

97 fluorescent signal was then obtained through fluorescence microscopy, and then quantified by ImageJ f

98 nanopore formation experiments and confocal fluorescence microscopy, and they can act as compartment

99 Here the authors use fluorescence microscopy approaches to directly visualize

100 Advances in fluorescence microscopy are providing increasing evidenc

101 r example, bright-field, phase contrast, and fluorescence microscopies, are unable to resolve 3D stru

102 Genetic and fluorescence-microscopy assays indicated that the Rec10

103 ditional single cell electrophysiological or fluorescence microscopy based methods.

104 Fluorescence microscopy-based in vitro reconstitution as

105 Combining fluorescence microscopy, biochemical interaction studies

106 um nanocell and single molecule/nanoparticle fluorescence microscopy can be extended to other systems

107 Contemporary fluorescence microscopy can detect individual virus part

108 he cell, but the limitations of conventional fluorescence microscopy can mask nanometer-scale feature

109 Steady state fluorescence microscopy cannot distinguish the drug from

110 On near-infrared fluorescence microscopy, CLIO-CyAm7 primarily deposited

111 Motorized fluorescence microscopy combined with high-throughput mi

112 nofluorescence and total internal reflection fluorescence microscopy confirmed that MHV-A59 used micr

113 MALDI-IMS) with confirmation by steady state fluorescence microscopy, creating a comprehensive pictur

114 By using fluorescence microscopy, cryogenic transmission electron

115 nal reference atlases and in vivo two-photon fluorescence microscopy data from the same specimen.

116 Fluorescence microscopy demonstrated intense labelling o

117 simply achieved using filter-free dark-field fluorescence microscopy (DFM).

118 s addressed by means of time-lapse automated fluorescence microscopy, electron microscopy, and immuno

119 Live-cell total internal reflection fluorescence microscopy, electrophysiology, and biochemi

120 The sensitivity provided by fluorescence microscopy enabled the observation of surfa

121 ion size and structure are now feasible with fluorescence microscopy (epifluorescence and CLSM imagin

122 Fluorescence microscopy examination of the cultures unde

123 To probe the mode of action, we performed fluorescence microscopy experiments on fungal cells trea

124 The NPs were also immunospecific in fluorescence microscopy experiments performed at room te

125 Fluorescence microscopy experiments showed that I2 coloc

126 This work features a series of longitudinal fluorescence microscopy experiments that characterize (1

127 For instance, fluorescence microscopy faces a 'colour barrier', owing

128 Fluorescence microscopy (FM) and electron microscopy (EM

129 identified cellular features of interest by fluorescence microscopy, followed by scanning transmissi

130 ric aberrations, to improve image quality of fluorescence microscopy for biological imaging.

131 ransformed infrared (FT-IR) spectroscopy and fluorescence microscopy for characterization of free and

132 Super-resolution fluorescence microscopy has become an invaluable, powerf

133 Light sheet fluorescence microscopy has previously been demonstrated

134 Smartphone fluorescence microscopy has various applications in poin

135 rent spectral unmixing methods for multiplex fluorescence microscopy have a limited ability to cope w

136 Advances in automated fluorescence microscopy have made snapshot and time-laps

137 echnologies, such as confocal or light sheet fluorescence microscopy have to utilize mechanical scann

138 High-speed fluorescence microscopy illuminated the versatile behavi

139 Colocalization analysis of fluorescence microscopy images is widely used to assess

140 Confocal fluorescence microscopy images of the perpendicular and

141 extracting realistic cell morphologies from fluorescence microscopy images to generate the piecewise

142 In conventional confocal/multiphoton fluorescence microscopy, images are typically acquired u

143 Total internal reflection fluorescence microscopy imaging revealed that vacuoles w

144 stains of vesicle substructures in confocal fluorescence microscopy imaging.

145 c interface states, and observe them through fluorescence microscopy in a passive PT-symmetric dimeri

146 Fluorescence microscopy in all tumor types demonstrated

147 We also utilized confocal fluorescence microscopy in mapped whole mount cochlear t

148 decarboxylase and ECP by flow cytometry and fluorescence microscopy in neutrophils from periodontiti

149 ematical modeling approach with quantitative fluorescence microscopy in two preclinical tumor models,

150 ility assays using total internal reflection fluorescence microscopy indicate that both Hook1 and Hoo

151 Northern blotting and fluorescence microscopy indicate that ORFX was expressed

152 s against Bacillus subtilis through confocal fluorescence microscopy indicated that Cu NCs showed str

153 Single-molecule fluorescence microscopy is a powerful tool for revealing

154 adherent cells by super-resolution far-field fluorescence microscopy is currently not possible becaus

155 idual cells of complex organs by electron or fluorescence microscopy is expensive and time consuming.

156 Consequently, the utility of X-ray fluorescence microscopy is intrinsically limited by the

157 Confocal fluorescence microscopy is often used in brain imaging e

158 Single-molecule fluorescence microscopy is uniquely suited for detecting

159 As an extension of wide-field fluorescence microscopy, it is inherently capable of mul

160 g findings were corroborated with intravital fluorescence microscopy (IVM), where nearly 90% of all f

161 tion of EV-releasing neurons using genetics, fluorescence microscopy, kymography, electron microscopy

162 Fluorescence microscopy, light microscopy and time domai

163 Light-sheet fluorescence microscopy (LSFM) enables high-speed, high-

164 Light Sheet Fluorescence Microscopy (LSFM) enables multi-dimensional

165 Light-sheet-based fluorescence microscopy (LSFM) features optical sectioni

166 The impact of light-sheet fluorescence microscopy (LSFM) is visible in fields as d

167 Light-sheet fluorescence microscopy (LSFM) serves to advance develop

168 , we combine this technique with light sheet fluorescence microscopy (LSFM) to visualize transplanted

169 d during dielectrophoretic manipulation with fluorescence microscopy making use of their fluorescence

170 immobilized on SU-8 surfaces is detected by fluorescence microscopy measurement after incubation wit

171 Using thousands of independent time-resolved fluorescence microscopy measurements in vivo, we show th

172 or microtubule assembly with nanometer-scale fluorescence microscopy measurements to identify the kin

173 Over the last decade, fluorescence microscopy methods have enabled the real-ti

174 e collected on days 0, 7, 14, 28, and 56 for fluorescence microscopy, micro-computed tomography, hist

175 Viewed by time-lapse epi-fluorescence microscopy, monocytes appeared to flutter r

176 s to place large amounts of volume data from fluorescence microscopy, morphed three-dimensionally, on

177 Prior to the development of super-resolution fluorescence microscopy (nanoscopy), investigation of en

178 tandard measure of cell proliferation, using fluorescence microscopy of 5-ethynyl-2'-deoxyuridine inc

179 tative analysis of high-throughput live-cell fluorescence microscopy of bacterial cells.

180 X-ray fluorescence microscopy of biological samples can map el

181 Fluorescence imaging of mouse eyes and fluorescence microscopy of dissected eye tissues from th

182 Fluorescence microscopy of FRET-based biosensors allow n

183 n 1A/1B-light chain 3) fractions, as well as fluorescence microscopy of LC3-GFP-overexpressing HeLa c

184 a combination of atomic force microscopy and fluorescence microscopy of live cells.

185 iscuss dose-appropriate guidelines for X-ray fluorescence microscopy of microscale biological samples

186 Fluorescence microscopy of sporulation-specific promoter

187 Confocal fluorescence microscopy of thin-sectioned lymphoid tissu

188 Fluorescence microscopy of wild-type mouse retina disclo

189 We employ fluorescence microscopy on non-polarized (human embryoni

190 uently use this alongside electrophysiology, fluorescence microscopy, optical coherence tomography (O

191 ical changes in the same cell using confocal fluorescence microscopy or STED.

192 eminal ganglion with 2-photon laser scanning fluorescence microscopy permitted visualization of DPANs

193 Multicolour light sheet fluorescence microscopy provided information about tsets

194 Fluorescence microscopy provides the ability to monitor

195 Conventional 3D laser scanning fluorescence microscopy requires repeated optical sectio

196 Pushing the frontier of fluorescence microscopy requires the design of enhanced

197 applied to samples prepared for conventional fluorescence microscopy, requiring no sophisticated samp

198 and mobility using total internal reflection fluorescence microscopy, resonance energy transfer, and

199 Ex vivo fluorescence microscopy revealed a large influx of macro

200 Interestingly, fluorescence microscopy revealed that FrzZ and FrzE loca

201 Fluorescence microscopy reveals that the contents of man

202 sessment of chemical modification induced in fluorescence microscopy settings with high sensitivity a

203 Confocal fluorescence microscopy showed that a fraction of HCF222

204 A deletion, EM and total internal reflection fluorescence microscopy showed that Syn-1A-KO beta-cells

205 The results from fluorescence microscopy showed that these probes specifi

206 lication was lower in abcb19 hypocotyls, and fluorescence microscopy showed the CCS52A2 protein to be

207 Fluorescence microscopy showed the localization of WH at

208 We have also correlated CARS with two-photon fluorescence microscopy simultaneously acquired using fl

209 ntegrated approach involving single-molecule fluorescence microscopy, single-particle cryo-electron m

210 The introduction of super-resolution fluorescence microscopy (SRM) opened an unprecedented vi

211 s) in diffraction limited and super-resolved fluorescence microscopy (STORM) experiments, we determin

212 lar evaluations, protein interaction assays, fluorescence microscopy, structural molecular modeling,

213 Fluorescence microscopy studies have shown that many pro

214 Improved capsid tags will facilitate fluorescence microscopy studies of virus particle intrac

215 analysis, orthogonal binding assays and cell fluorescence microscopy studies reveal a strong anti-cor

216 nceptually, AcroB provides a new paradigm on fluorescence microscopy studies where chemical perturbat

217 rs to biological questions obtained via live fluorescence microscopy substantially affected by photot

218 s of cellular location by immunolabeling and fluorescence microscopy suggests that BoMan26B is surfac

219 In this study, we have used super-resolution fluorescence microscopy supplemented by fluorescence cor

220 in nanoscale topography)-a super-resolution fluorescence microscopy technique that exploits programm

221 We used a combined atomic force microscopy/fluorescence microscopy technique to determine the mecha

222 (40 +/- 5 mum diameter) using a streak-based fluorescence microscopy technique.

223 ite its short history, diffraction-unlimited fluorescence microscopy techniques have already made a s

224 However, fluorescence microscopy techniques reveal a more dynamic

225 y (SR-SIM) is among the most rapidly growing fluorescence microscopy techniques that can surpass the

226 century has witnessed rapid developments of fluorescence microscopy techniques that enable structura

227 reach this conclusion, we combined different fluorescence microscopy techniques, including superresol

228 croparticles (micro-PS) using electronic and fluorescence microscopy techniques.

229 ibes a novel approach to spectrally resolved fluorescence microscopy, termed sensorFRET, that enables

230 Here we show using total internal reflection fluorescence microscopy that KlpA-a kinesin-14 from Aspe

231 age with two-color total internal reflection fluorescence microscopy the local changes of 27 proteins

232 D and RH-RhB were employed to investigate by fluorescence microscopy the self-sorting and coassembly

233 Using total internal reflection fluorescence microscopy, the fusion of single DCVs with

234 Together with fluorescence microscopy, the simulations show that prote

235 g) cell (Chlorella vulgaris) as confirmed by fluorescence microscopy, thermogravimetric analysis (TGA

236 pletion (GSD), and total internal reflection fluorescence microscopy (TIRF) that a proportion of ARHG

237 e resolution using total internal reflection fluorescence microscopy (TIRF).

238 oteins by in vitro total internal reflection fluorescence microscopy (TIRFM) and kinetic and thermody

239 Total internal reflection fluorescence microscopy (TIRFM) is well suited to focus

240 ocampal neurons by total internal reflection fluorescence microscopy (TIRFM).

241 Using light-sheet fluorescence microscopy to address the challenges associ

242 We use optical tweezers microrheology and fluorescence microscopy to apply nonlinear microscale st

243 ight dextran molecule, which was shown using fluorescence microscopy to be localized around the hair

244 usion assays using total internal reflection fluorescence microscopy to compare hemifusion kinetics a

245 used confocal and total internal reflection fluorescence microscopy to count the number of Mcp5 foci

246 we used multicolor total internal reflection fluorescence microscopy to directly observe actin assemb

247 Here, using time-lapse fluorescence microscopy to examine PhoP-dependent gene e

248 c force microscopy (AFM) and single molecule fluorescence microscopy to examine the interactions of P

249 loped a cell-based screening assay that uses fluorescence microscopy to identify APJ antagonists.

250 ome conformation capture in combination with fluorescence microscopy to investigate Heat Shock Protei

251 s work, we have used wide-field and confocal fluorescence microscopy to investigate the spatial organ

252 d used a combination of optical tweezers and fluorescence microscopy to measure the interactions of s

253 Here, we use fluorescence microscopy to measure Tmix and we use atomi

254 bacteriological manipulation and light sheet fluorescence microscopy to monitor the dynamics of a def

255 roparticles, in both cases using light-sheet fluorescence microscopy to optically access the intestin

256 We used total internal reflection fluorescence microscopy to quantify fusion-pore dynamics

257 ng matrix by atomic force microscopy and use fluorescence microscopy to relate those properties to ch

258 We used single-molecule fluorescence microscopy to show that the MT plus-end-ass

259 We combine Nomarski and multichannel fluorescence microscopy to study processes such as cell-

260 We used single-molecule fluorescence microscopy to study self-diffusion of a fee

261 zed soft X-ray tomography (SXT) coupled with fluorescence microscopy to study the detailed structures

262 To investigate their functions, we used fluorescence microscopy to survey early, middle, and lat

263 Here we used single-molecule fluorescence microscopy to visualize how Bacillus subtil

264 ent observation in total internal reflection fluorescence microscopy, to examine relevant functions o

265 tion to integrate high-resolution two-photon fluorescence microscopy (TPM) with a 16.4 tesla MRI syst

266 We combined mass spectrometry, fluorescence microscopy, transmission electron microscop

267 tions were observed in real time by confocal fluorescence microscopy using a Bodipy fluorogenic subst

268 Typically, particle tracks are obtained from fluorescence microscopy video images, although this limi

269 Total internal reflection fluorescence microscopy was performed to image the confo

270 Successful visualization by fluorescence microscopy was possible with a reagent conc

271 Total internal reflection fluorescence microscopy was used to probe binding and re

272 In this work, single-molecule fluorescence microscopy was used to study the adsorption

273 alance is easy to handle and compatible with fluorescence microscopy, we anticipate that our approach

274 Using live-cell fluorescence microscopy, we captured 2,330 hours of tumo

275 Using dual-color total internal reflection fluorescence microscopy, we demonstrate complex formatio

276 Using combined atomic force and confocal fluorescence microscopy, we demonstrate that the ACes en

277 Using single-molecule fluorescence microscopy, we determined in vivo stoichiom

278 Using intracellular flow cytometry and fluorescence microscopy, we determined that T. gondii in

279 Using ultraviolet fluorescence microscopy, we directly track drug accumula

280 lecule multi-color total internal reflection fluorescence microscopy, we discovered that sorting of t

281 ng single-molecule total internal reflection fluorescence microscopy, we examined the rotational conf

282 Using microfluidics combined with fluorescence microscopy, we extract quantitative informa

283 By examining replisomes in live E. coli with fluorescence microscopy, we found that the Pol III* suba

284 Using quantitative fluorescence microscopy, we measure changes in the dista

285 Using multiwavelength single-molecule fluorescence microscopy, we observed the dynamics of Gre

286 Using in vitro total internal reflection fluorescence microscopy, we show that bacterial mini mic

287 okes Raman scattering and two-photon excited fluorescence microscopy, we show that CDCP1 depletes lip

288 microscopy mechanical mapping combined with fluorescence microscopy, we show that higher Young's mod

289 Using total internal reflection fluorescence microscopy, we show that the membrane-bound

290 Combining electrochemical perturbation and fluorescence microscopy, we show that the potential at w

291 ging, histological examination, and confocal fluorescence microscopy were used to identify early entr

292 rotome sectioning, differential staining and fluorescence microscopy were used to visualize patterns

293 Three-dimensional light-sheet fluorescence microscopy with Cy5-Fab-PAS200 confirmed be

294 Fluorescence microscopy with marker proteins showed that

295 By performing quantitative fluorescence microscopy with microfuidics, we investigat

296 we used polarized total internal reflection fluorescence microscopy with nanometer accuracy localiza

297 lysis (HCA) approach that combines automated fluorescence microscopy with real-time quantitative imag

298 n reaction (HOR), we combine single-molecule fluorescence microscopy with traditional electrochemical

299 X-ray fluorescence microscopy (XFM) and X-ray absorption near-

300 Here we employ synchrotron-based X-ray fluorescence microscopy (XFM) to map and quantify physio