ライフサイエンスコーパス: total internal reflection fluorescence

1 orescence) or immobilized on surfaces (using total-internal-reflection fluorescence).

2 images from both atomic force microscopy and total internal reflection fluorescence.

3 ed fluorescence), and were imaged live using total internal reflection fluorescence and confocal micr

4 fluctuation spectroscopy in conjunction with total internal reflection fluorescence and conventional,

5 ligand-occupied alphaIIbbeta3 as revealed by total internal reflection fluorescence and electron micr

6 olution is maximized by concurrently applied total internal reflection fluorescence and epifluorescen

7 we demonstrate the versatility of a combined total internal reflection fluorescence and scanning forc

8 on study in scanning electron microscopy and total internal reflection fluorescence and scattering mi

9 We used magnetic tweezers, total internal reflection fluorescence, and atomic force

10 Using a combination of live confocal, total internal reflection fluorescence, and superresolut

11 Electron microscope and total internal reflection fluorescence-based assays were

12 Data generated with total internal reflection fluorescence-based fluorescenc

13 Total internal reflection fluorescence-based single-mole

14 The total internal reflection fluorescence-based vesicle bin

15 Therefore, we used imaging total internal reflection-fluorescence correlation spect

16 A recent study using imaging total internal reflection-fluorescence correlation spect

17 Further fundamental investigations applying total internal reflection fluorescence detection for kin

18 chamber designed for isometric contraction, total internal reflection fluorescence detection, and tw

19 eal that L-selectin has the highest ratio of total internal reflection fluorescence/epi intensity, an

20 quencher-labeled biomolecules can be used in total-internal-reflection fluorescence experiments at co

21 n this study, we developed a liposome-based, total internal reflection fluorescence, fiber-optic bios

22 Total internal reflection fluorescence from CoroNa Green

23 To overcome this challenge, we analyzed total internal reflection fluorescence images of migrati

24 unit area in epi-fluorescence images versus total internal reflection fluorescence images provides a

25 Total internal reflection fluorescence imaging and elect

26 n expression, we performed biotinylation and total internal reflection fluorescence imaging assays; h

27 Total internal reflection fluorescence imaging indicated

28 We utilized total internal reflection fluorescence imaging of Ca(2+)

29 We used total internal reflection fluorescence imaging of living

30 Time-lapse total internal reflection fluorescence imaging of M23 in

31 Single-motor total internal reflection fluorescence imaging of YFP-Mo

32 Total internal reflection fluorescence imaging revealed

33 of their integral membrane-proteins, we used total internal reflection fluorescence imaging to study

34 al membrane protein expression, we performed total internal reflection fluorescence imaging, which re

35 Using a total internal reflection fluorescence imaging-based app

36 ophysiology, cell surface biotinylation, and total internal reflection fluorescence live cell imaging

37 present the development of a two-wavelength total internal reflection fluorescence method capable of

38 otocol for constructing a CoSMoS micromirror total internal reflection fluorescence microscope (mmTIR

39 plications under an automated scanning-angle total internal reflection fluorescence microscope (SA-TI

40 Total internal reflection fluorescence microscope (TIRFM

41 ic calibration and scanning-angle prism-type total internal reflection fluorescence microscope (TIRFM

42 escent primary-secondary antibody complexes, total internal reflection fluorescence microscopic imagi

43 s investigated using polarization optics and total internal reflection fluorescence microscopy (pTIRF

44 ination of quantitative live-cell imaging by total internal reflection fluorescence microscopy (TIR-F

45 We used total internal reflection fluorescence microscopy (TIR-F

46 opy (SIM), ground-state depletion (GSD), and total internal reflection fluorescence microscopy (TIRF)

47 and at the single-particle resolution using total internal reflection fluorescence microscopy (TIRF)

48 nd slow elongating VASP proteins by in vitro total internal reflection fluorescence microscopy (TIRFM

49 Total internal reflection fluorescence microscopy (TIRFM

50 level of individual endocytic events using a total internal reflection fluorescence microscopy (TIRFM

51 lation on the plasma membrane as revealed by total internal reflection fluorescence microscopy (TIRFM

52 eriments, using a unique method to carry out total internal reflection fluorescence microscopy (TIRFM

53 Total internal reflection fluorescence microscopy (TIRFM

54 eir assembly to make a clot were observed by total internal reflection fluorescence microscopy (TIRFM

55 othelial cells using a unique combination of total internal reflection fluorescence microscopy (TIRFM

56 With the use of single-molecule total internal reflection fluorescence microscopy (TIRFM

57 rder to start addressing this issue, we used total internal reflection fluorescence microscopy (TIRFM

58 s and impaired in type II diabetes, by using total internal reflection fluorescence microscopy (TIRFM

59 Total internal reflection fluorescence microscopy (TIRFM

60 Here we use total internal reflection fluorescence microscopy (TIRFM

61 fficking of DAT to the plasma membrane using total internal reflection fluorescence microscopy (TIRFM

62 NMDA receptors in rat hippocampal neurons by total internal reflection fluorescence microscopy (TIRFM

63 Total internal reflection fluorescence microscopy (TIRFM

64 We used these nanopores with AFM and total internal reflection fluorescence microscopy (TIRFM

65 Total internal reflection fluorescence microscopy (TIRFM

66 Total internal reflection fluorescence microscopy (TIRFM

67 ropose an improved version of variable-angle total internal reflection fluorescence microscopy (vaTIR

68 determined by Raman spectroscopy mapping and total internal reflection fluorescence microscopy analys

69 multiscale, live cell imaging (confocal and total internal reflection fluorescence microscopy and a

70 Using total internal reflection fluorescence microscopy and a

71 We have used total internal reflection fluorescence microscopy and a

72 e within the plasma membrane using polarized total internal reflection fluorescence microscopy and am

73 Total Internal Reflection Fluorescence microscopy and bi

74 ynthesis and turnover on CME by quantitative total internal reflection fluorescence microscopy and co

75 n in cultured rat brainstem astrocytes using total internal reflection fluorescence microscopy and fo

76 Total internal reflection fluorescence microscopy and hi

77 ing dynamic imaging modalities (confocal and total internal reflection fluorescence microscopy and lu

78 obacter crescentus near a glass surface with total internal reflection fluorescence microscopy and ob

79 e focus on recent studies that have employed total internal reflection fluorescence microscopy and ot

80 Using total internal reflection fluorescence microscopy and qu

81 PLM combines polarized total internal reflection fluorescence microscopy and si

82 d actin cytoskeleton within live cells using total internal reflection fluorescence microscopy and si

83 Using total internal reflection fluorescence microscopy and st

84 Single Qdots were imaged in time with total internal reflection fluorescence microscopy and th

85 aining planar membranes are distinguished by total internal reflection fluorescence microscopy as sep

86 P(i)) under zero load in the single-molecule total internal reflection fluorescence microscopy assay.

87 ulk actin polymerization and single filament total internal reflection fluorescence microscopy assays

88 Immunofluorescence and total internal reflection fluorescence microscopy confir

89 Moreover, total internal reflection fluorescence microscopy experi

90 Additionally, total internal reflection fluorescence microscopy experi

91 However, total internal reflection fluorescence microscopy experi

92 Fluorescence resonance energy transfer and total internal reflection fluorescence microscopy experi

93 In real-time total internal reflection fluorescence microscopy experi

94 In our study total internal reflection fluorescence microscopy images

95 Here, using multicolor total internal reflection fluorescence microscopy imagin

96 Total internal reflection fluorescence microscopy imagin

97 Total internal reflection fluorescence microscopy imagin

98 Total internal reflection fluorescence microscopy imagin

99 n a membrane using live cell high resolution total internal reflection fluorescence microscopy in con

100 ine triphosphatase) at the cell cortex using total internal reflection fluorescence microscopy in fla

101 Using total internal reflection fluorescence microscopy in liv

102 Western blots and single-vesicle imaging by total internal reflection fluorescence microscopy in liv

103 ith the use of ecliptic pHluorin-fused ER46, total internal reflection fluorescence microscopy in liv

104 pressed in Chinese hamster ovary cells under total internal reflection fluorescence microscopy in whi

105 In the patients' fibroblasts, total internal reflection fluorescence microscopy indica

106 Single-molecule motility assays using total internal reflection fluorescence microscopy indica

107 greement with classical measurements made by total internal reflection fluorescence microscopy involv

108 protease activity at the PM, demonstrated by total internal reflection fluorescence microscopy of a c

109 Model predictions were tested by total internal reflection fluorescence microscopy of AQP

110 We used total internal reflection fluorescence microscopy of IFT

111 Total internal reflection fluorescence microscopy of the

112 We have used a combination of total internal reflection fluorescence microscopy of tra

113 Real-time total internal reflection fluorescence microscopy reveal

114 Total internal reflection fluorescence microscopy reveal

115 Total internal reflection fluorescence microscopy reveal

116 Total internal reflection fluorescence microscopy reveal

117 Total internal reflection fluorescence microscopy reveal

118 eaching experiments and particle tracking by total internal reflection fluorescence microscopy reveal

119 ellular localization studies by confocal and total internal reflection fluorescence microscopy reveal

120 Polarized total internal reflection fluorescence microscopy reveal

121 Confocal and live total internal reflection fluorescence microscopy showed

122 Single molecule total internal reflection fluorescence microscopy showed

123 Total internal reflection fluorescence microscopy showed

124 ic defects caused by Syn-1A deletion, EM and total internal reflection fluorescence microscopy showed

125 f quantum-dot-labeled AQP4 in live cells and total internal reflection fluorescence microscopy showed

126 Total internal reflection fluorescence microscopy showed

127 Here we show using total internal reflection fluorescence microscopy that K

128 Here we image with two-color total internal reflection fluorescence microscopy the lo

129 erformed single-particle fusion assays using total internal reflection fluorescence microscopy to com

130 We used confocal and total internal reflection fluorescence microscopy to cou

131 Here we use single molecule total internal reflection fluorescence microscopy to det

132 ns of the DNA strand exchange reactions with total internal reflection fluorescence microscopy to det

133 Here, we used multicolor total internal reflection fluorescence microscopy to dir

134 these differences, we used multi-wavelength total internal reflection fluorescence microscopy to dir

135 direct receptor labeling with SNAP-tags and total internal reflection fluorescence microscopy to dyn

136 To address this, we used single molecule total internal reflection fluorescence microscopy to exa

137 In this study, we used total internal reflection fluorescence microscopy to ima

138 We introduce here the use of total internal reflection fluorescence microscopy to ima

139 8 membrane dye were used in combination with total internal reflection fluorescence microscopy to mea

140 In this work, we used live-cell total internal reflection fluorescence microscopy to mon

141 Using total internal reflection fluorescence microscopy to mon

142 We used total internal reflection fluorescence microscopy to obs

143 We used single-molecule total internal reflection fluorescence microscopy to pro

144 Using total internal reflection fluorescence microscopy to qua

145 We used total internal reflection fluorescence microscopy to qua

146 Here we use total internal reflection fluorescence microscopy to sho

147 Here we have used patch-clamp recordings and total internal reflection fluorescence microscopy to stu

148 is distinct region of the cell, we have used total internal reflection fluorescence microscopy to stu

149 vesicle release in salamander rods by using total internal reflection fluorescence microscopy to vis

150 underlying their cellular functions we used total internal reflection fluorescence microscopy to vis

151 State transitions were visualized by total internal reflection fluorescence microscopy using

152 Total internal reflection fluorescence microscopy was pe

153 Total internal reflection fluorescence microscopy was us

154 ng mechanism in real time, we used polarized total internal reflection fluorescence microscopy with n

155 ted using atomic force microscopy, polarized total internal reflection fluorescence microscopy, and N

156 robe illumination volume was minimized using total internal reflection fluorescence microscopy, and P

157 mologs, we applied fluorescence confocal and total internal reflection fluorescence microscopy, and s

158 Although Blue Native-PAGE, total internal reflection fluorescence microscopy, and w

159 concepts of fluorescent speckle microscopy, total internal reflection fluorescence microscopy, atomi

160 Live-cell total internal reflection fluorescence microscopy, elect

161 Here, we combine bulk assays, total internal reflection fluorescence microscopy, fluor

162 We use single-molecule total internal reflection fluorescence microscopy, in co

163 tment of which could be directly observed by total internal reflection fluorescence microscopy, in re

164 With the use of total internal reflection fluorescence microscopy, it wa

165 Single molecules of Myo52p, visualized by total internal reflection fluorescence microscopy, moved

166 ons, spatial arrangement, and mobility using total internal reflection fluorescence microscopy, reson

167 By combining total internal reflection fluorescence microscopy, singl

168 Here, we show using patch clamp analysis and total internal reflection fluorescence microscopy, that

169 Through the use of single-molecule total internal reflection fluorescence microscopy, the d

170 Using total internal reflection fluorescence microscopy, the f

171 Using total internal reflection fluorescence microscopy, the n

172 opy and single actin filament observation in total internal reflection fluorescence microscopy, to ex

173 ing microfluidic flow channels combined with total internal reflection fluorescence microscopy, we ap

174 Using dual-color total internal reflection fluorescence microscopy, we de

175 ing genetically manipulated mouse models and total internal reflection fluorescence microscopy, we de

176 Using dual-color total internal reflection fluorescence microscopy, we de

177 Under total internal reflection fluorescence microscopy, we de

178 ly visualizing actin filament assembly using total internal reflection fluorescence microscopy, we de

179 metic assays and single-molecule multi-color total internal reflection fluorescence microscopy, we di

180 Using single-molecule total internal reflection fluorescence microscopy, we ex

181 Using total internal reflection fluorescence microscopy, we ex

182 Using total internal reflection fluorescence microscopy, we fo

183 ro actin polymerization assay and time-lapse total internal reflection fluorescence microscopy, we fo

184 Furthermore, by use of the triple-color total internal reflection fluorescence microscopy, we fo

185 Using total internal reflection fluorescence microscopy, we ob

186 Using multiple-color live-cell total internal reflection fluorescence microscopy, we ob

187 Using total internal reflection fluorescence microscopy, we re

188 Using total internal reflection fluorescence microscopy, we re

189 With total internal reflection fluorescence microscopy, we re

190 lasma membrane of live cells is monitored by total internal reflection fluorescence microscopy, we se

191 Using rapid time-lapse total internal reflection fluorescence microscopy, we sh

192 Using scanning mutagenesis and total internal reflection fluorescence microscopy, we sh

193 y using a combination of structural work and total internal reflection fluorescence microscopy, we sh

194 n/retraction and PI3K signaling monitored by total internal reflection fluorescence microscopy, we sh

195 Using in vitro total internal reflection fluorescence microscopy, we sh

196 analysis of a novel VLA-4 FRET sensor under total internal reflection fluorescence microscopy, we sh

197 Using total internal reflection fluorescence microscopy, we sh

198 Using multi-color total internal reflection fluorescence microscopy, we sh

199 Using confocal and total internal reflection fluorescence microscopy, we st

200 We use multicolor, dual-penetration depth, total internal reflection fluorescence microscopy, which

201 ein-p150(Glued) co-complex using dual-colour total internal reflection fluorescence microscopy.

202 t submembrane regions visualized by confocal total internal reflection fluorescence microscopy.

203 nslational modifications were analyzed using total internal reflection fluorescence microscopy.

204 , fluorescence correlation spectroscopy, and total internal reflection fluorescence microscopy.

205 by PcrA/RepD was followed in real-time using total internal reflection fluorescence microscopy.

206 mbly using both bulk fluorescence assays and total internal reflection fluorescence microscopy.

207 patio-temporally dissociated, as detected by total internal reflection fluorescence microscopy.

208 id bilayer is measured using single-molecule total internal reflection fluorescence microscopy.

209 n components in migrating cells imaged using total internal reflection fluorescence microscopy.

210 gle-virion fusion events are monitored using total internal reflection fluorescence microscopy.

211 re vesicles (LDCVs) in live PC12 cells using total internal reflection fluorescence microscopy.

212 ng conventional far-field epifluorescence or total internal reflection fluorescence microscopy.

213 coded unambiguously using epifluorescence or total internal reflection fluorescence microscopy.

214 rescence microscopy, cell fractionation, and total internal reflection fluorescence microscopy.

215 me, binds and severs MTs via single molecule total internal reflection fluorescence microscopy.

216 re observed in real time via single-molecule total internal reflection fluorescence microscopy.

217 CPs, as determined by quantitative live-cell total internal reflection fluorescence microscopy.

218 splaying ligands for immunoglobulin E, using total internal reflection fluorescence microscopy.

219 -stranded DNA product of the helicase, using total internal reflection fluorescence microscopy.

220 e we used pHluorin-tagged GluA2 subunits and total internal reflection fluorescence microscopy.

221 on of STIM1 can be observed in some cells by total internal reflection fluorescence microscopy.

222 hR beta19'Lys(BODIPYFL), using time-resolved total internal reflection fluorescence microscopy.

223 lambda-repressor CI and its target DNA using total internal reflection fluorescence microscopy.

224 ence resonance energy transfer measured with total internal reflection fluorescence microscopy.

225 interface as a function of temperature using total internal reflection fluorescence microscopy.

226 membranous calcium signal was assessed using total internal reflection fluorescence microscopy.

227 e mechanism of DNA condensation by BAF using total internal reflection fluorescence microscopy.

228 GTP addition when viewed in real time using total internal reflection fluorescence microscopy.

229 single-molecule resolution using time-lapse total internal reflection fluorescence microscopy.

230 g in the presence of VASP and profilin using total internal reflection fluorescence microscopy.

231 microfluidic techniques in conjunction with total internal reflection fluorescence microscopy.

232 ctivity were monitored in real time by using total internal reflection fluorescence microscopy.

233 a dynamic microtubule assay and examined by total internal reflection fluorescence microscopy.

234 confirmed in in vitro synaptosomes by using total internal reflection fluorescence microscopy.

235 of human Cof1, Cof2, and ADF using in vitro total internal reflection fluorescence microscopy.

236 eir behavior at the plasma membrane by using total internal reflection fluorescence microscopy.

237 assays and direct visualization by two-color total internal reflection fluorescence microscopy.

238 y operating single-molecule, objective-type, total internal reflection fluorescence microscopy.

239 using freely in solution were observed using total internal reflection fluorescence microscopy.

240 by vesicle-mediated exocytosis visualized by total internal reflection fluorescence microscopy.

241 high-resolution atomic force, confocal, and total internal reflection fluorescence microscopy.

242 teractions near the plasma membrane by using total internal reflection fluorescence microscopy.

243 e in OAPs; 2) OAPs can be imaged directly by total internal reflection fluorescence microscopy; and 3

244 and membrane-associated vesicles measured by total internal reflection-fluorescence microscopy was de

245 end-residency time, along microtubules in a total internal-reflection fluorescence microscopy assay.

246 veloped a single molecule system using TIRF (total internal reflection fluorescence) microscopy and p

247 lation number and brightness analysis to the total internal reflection fluorescence modality, we were

248 s and to filopodia-like structures imaged by total internal reflection fluorescence on the basal surf

249 cord with the inference drawn from polarized total internal reflection fluorescence (polTIRF) experim

250 We used high-speed polarized total internal reflection fluorescence (polTIRF) microsc

251 cation detected by single-molecule polarized total internal reflection fluorescence (polTIRF) microsc

252 tracked conformational changes in SNAP25 by total internal reflection fluorescence resonance energy

253 short nucleosome arrays with single molecule total internal reflection fluorescence (smTIRF) microsco

254 We combine total internal reflection fluorescence structured illumi

255 ng of the endogenous proteins, and two-color total internal reflection fluorescence structured-illumi

256 Using total internal reflection fluorescence (TIRF) and confoc

257 t of detection (LOD) with respect to regular total internal reflection fluorescence (TIRF) configurat

258 (EW) excitation isotropic, thereby producing total internal reflection fluorescence (TIRF) images tha

259 In addition, total internal reflection fluorescence (TIRF) imaging wa

260 ackground fluorescence than is achieved with total internal reflection fluorescence (TIRF) imaging.

261 lution optical sectioning using a multiangle total internal reflection fluorescence (TIRF) microscope

262 Furthermore, total internal reflection fluorescence (TIRF) microscopy

263 Using high-resolution total internal reflection fluorescence (TIRF) microscopy

264 By total internal reflection fluorescence (TIRF) microscopy

265 Here, we use total internal reflection fluorescence (TIRF) microscopy

266 Total internal reflection fluorescence (TIRF) microscopy

267 fected Vero cells by electron, confocal, and total internal reflection fluorescence (TIRF) microscopy

268 leading to surface expression as assessed by total internal reflection fluorescence (TIRF) microscopy

269 Time-lapse total internal reflection fluorescence (TIRF) microscopy

270 ntional pull-down assay with single-molecule total internal reflection fluorescence (TIRF) microscopy

271 rafficking in living 3T3-L1 adipocytes using total internal reflection fluorescence (TIRF) microscopy

272 Here, time-lapse total internal reflection fluorescence (TIRF) microscopy

273 We distinguished between these using total internal reflection fluorescence (TIRF) microscopy

274 Using total internal reflection fluorescence (TIRF) microscopy

275 cence resonance energy transfer (FRET) under total internal reflection fluorescence (TIRF) microscopy

276 e energy transfer (FRET) stoichiometry under total internal reflection fluorescence (TIRF) microscopy

277 Time-lapse epifluorescence, total internal reflection fluorescence (TIRF) microscopy

278 bserved directly with time-lapse imaging and total internal reflection fluorescence (TIRF) microscopy

279 Here we use a sensitive total internal reflection fluorescence (TIRF) microscopy

280 ndance proteins to be counted using standard total internal reflection fluorescence (TIRF) microscopy

281 1 cells using video-rate epifluorescence and total internal reflection fluorescence (TIRF) microscopy

282 CaM expressed in CHO cells, performed under total internal reflection fluorescence (TIRF) microscopy

283 Total internal reflection fluorescence (TIRF) microscopy

284 Furthermore, in vitro total internal reflection fluorescence (TIRF) microscopy

285 Fast dual-color total internal reflection fluorescence (TIRF) microscopy

286 active coating materials in combination with total internal reflection fluorescence (TIRF) microscopy

287 Single-molecule total internal reflection fluorescence (TIRF) microscopy

288 Total internal reflection fluorescence (TIRF) microscopy

289 d single molecules of SSB-coated ssDNA using total internal reflection fluorescence (TIRF) microscopy

290 Furthermore, two-color total internal reflection fluorescence (TIRF) microscopy

291 nce Recovery after Photobleaching (FRAP) and Total Internal Reflection Fluorescence (TIRF) microscopy

292 single molecule level was accomplished using total internal reflection fluorescence (TIRF) with fluor

293 nd to be required for vesicle capture in the total internal reflection fluorescence (TIRF) zone benea

294 Here, we employ an optical-trap- and total internal reflection fluorescence (TIRF)-based assa

295 anoscale ( approximately 2-10 nm); smFRET in total-internal reflection fluorescence (TIRF) Forster re

296 Total-internal reflection fluorescence (TIRF) imaging is

297 ual resorufin molecules can be studied using total-internal reflection fluorescence (TIRF).

298 neutravidin molecules is measured in situ by total-internal-reflection fluorescence (TIRF) microscopy

299 Total-Internal-Reflection-Fluorescence (TIRF) microscopy

300 use site-directed spin labeling and a novel total internal reflection fluorescence vesicle binding a