ライフサイエンスコーパス: confocal fluorescence microscopy

1 and the mapping of concentration profiles by confocal fluorescence microscopy.

2 on of DnaA in living cells was visualized by confocal fluorescence microscopy.

3 The films were imaged by confocal fluorescence microscopy.

4 lls (L1210FR leukemia cell line) by means of confocal fluorescence microscopy.

5 be immediately examined by conventional and confocal fluorescence microscopy.

6 mmunohistochemistry, isolectin staining, and confocal fluorescence microscopy.

7 were co-localized with iNOS as determined by confocal fluorescence microscopy.

8 rface TGF-beta on Foxp3+CD4+CD25+ T cells in confocal fluorescence microscopy.

9 nd their subcellular locations determined by confocal fluorescence microscopy.

10 ed of DOPC/DPPC or DLPC/DPPC are observed by confocal fluorescence microscopy.

11 NA also could be detected over background by confocal fluorescence microscopy.

12 he detection of single protein molecules via confocal fluorescence microscopy.

13 neously in live explants using spinning disk confocal fluorescence microscopy.

14 cribe a protocol for interfacing 3D-MTC with confocal fluorescence microscopy.

15 ther beta1AR trafficked to lysosomes we used confocal fluorescence microscopy.

16 issues were imaged using epifluorescence and confocal fluorescence microscopy.

17 immunoprecipitation assays and visualized by confocal fluorescence microscopy.

18 single-photon counting coupled with scanning confocal fluorescence microscopy.

19 fluorescent protein translocation assays and confocal fluorescence microscopy.

20 protein on the plasma membrane, as judged by confocal fluorescence microscopy.

21 o study their trafficking pattern in vivo by confocal fluorescence microscopy.

22 ullary collecting duct (IMCD) segments using confocal fluorescence microscopy.

23 by subcellular fractionation studies and by confocal fluorescence microscopy.

24 llary is directly imaged with laser scanning confocal fluorescence microscopy.

25 er of hippocampal synapses using FM 1-43 and confocal fluorescence microscopy.

26 in endothelial F-actin was determined using confocal fluorescence microscopy.

27 and localization patterns monitored by using confocal fluorescence microscopy.

28 ofluorometer, and the cells were examined by confocal fluorescence microscopy.

29 f IL-12, as determined by flow cytometry and confocal fluorescence microscopy.

30 jacent to the plasma membrane as detected by confocal fluorescence microscopy.

31 distribution of this receptor as detected by confocal fluorescence microscopy.

32 were partially colocalized, as determined by confocal fluorescence microscopy.

33 L-2, altered actin morphology as assessed by confocal fluorescence microscopy.

34 nals from single neurons with laser scanning confocal fluorescence microscopy.

35 utophagosome marker, by Western blotting and confocal fluorescence microscopy.

36 mide-alkyne, and to image oxidized thiols by confocal fluorescence microscopy.

37 e tomography (OCT), Brillouin microscopy and confocal fluorescence microscopy.

38 this approach in wide-field, two-photon, and confocal fluorescence microscopy.

39 elease as demonstrated by flow cytometry and confocal fluorescence microscopy.

40 on of dyes and imaging of tagged proteins by confocal fluorescence microscopy.

41 pressing DsRed (Discosoma sp.) and imaged by confocal fluorescence microscopy.

42 of the crypts which were assayed in situ by confocal fluorescence microscopy.

43 cal actin dynamics simultaneously by AFM and confocal fluorescence microscopy.

44 rmed by transmission electron microscopy and confocal fluorescence microscopy.

45 stallites are also estimated with the use of confocal fluorescence microscopy.

46 with respect to those of Min as revealed by confocal fluorescence microscopy.

47 or metastasis, and results were confirmed by confocal fluorescence microscopy.

48 of the transmembrane protein was analyzed by confocal fluorescence microscopy.

49 intracellular localization was evaluated via confocal fluorescence microscopy.

50 vidual live DM1 model cells using time-lapse confocal fluorescence microscopy.

51 ative extracellular oxidant distributions by confocal fluorescence microscopy.

52 heir cellular localization was visualized by confocal fluorescence microscopy.

53 complex was illustrated through live imaging confocal fluorescence microscopy.

54 sformation of 1 to 2 inside such cells using confocal fluorescence microscopy.

55 ecies inside the cells has been evaluated by confocal fluorescence microscopy.

56 racellular bioorthogonal probe, as judged by confocal fluorescence microscopy.

57 e corroborated with immunohistochemistry and confocal fluorescence microscopy.

58 les was examined in real time wide-field and confocal fluorescence microscopy.

59 os and FG in CeA neurons was visualized with confocal-fluorescence microscopy.

60 Using laser scanning confocal fluorescence microscopy, alternans of electrica

61 hromaffin granule exocytosis were studied by confocal fluorescence microscopy, amperometry, and cell-

62 Confocal fluorescence microscopy and a lymphoid enhancer

63 on a unique combination of laboratory-based confocal fluorescence microscopy and advanced image proc

64 Using confocal fluorescence microscopy and analysis of oligosa

65 n analyte dispersion was characterized using confocal fluorescence microscopy and electrochemical det

66 Subcellular-resolution ex vivo imaging using confocal fluorescence microscopy and electron microscopy

67 ith uncoupled Cu(II) centres as evidenced by confocal fluorescence microscopy and electron paramagnet

68 ngle living cells has been achieved by using confocal fluorescence microscopy and externally tagged p

69 We then use confocal fluorescence microscopy and flow cytometry to d

70 Confocal fluorescence microscopy and fluorescence resona

71 or the visualization of peptide receptors by confocal fluorescence microscopy and for the enrichment

72 luding atomic force microscopy combined with confocal fluorescence microscopy and Fourier transform i

73 ia were imaged and chemically analyzed using confocal fluorescence microscopy and Fourier-transform i

74 Standard and confocal fluorescence microscopy and image analysis were

75 Confocal fluorescence microscopy and immunohistochemistr

76 Further investigations by confocal fluorescence microscopy and immunoprecipitation

77 This method uses confocal fluorescence microscopy and involves approximat

78 Scanning confocal fluorescence microscopy and multiphoton fluores

79 Confocal fluorescence microscopy and proliferation/viabi

80 ic-field-induced mechanical stimulation with confocal fluorescence microscopy and provides an optiona

81 nity reagents suitable for western blotting, confocal fluorescence microscopy and pull-down applicati

82 ased in the Vit D-preconditioned cultures by confocal fluorescence microscopy and semiquantitative im

83 sh medial giant axons (MGAs) with time-lapse confocal fluorescence microscopy and showed that many in

84 are consistent with similar measurements by confocal fluorescence microscopy and subcellular fractio

85 endogenous syntaxin 6 as determined both by confocal fluorescence microscopy and subcellular fractio

86 Quantitative confocal fluorescence microscopy and surface biotinylati

87 GUVs were imaged by confocal fluorescence microscopy and then analyzed for c

88 Hyperspectral confocal fluorescence microscopy and three-dimensional s

89 Confocal fluorescence microscopy and uptake kinetic anal

90 oma cells, and the results are compared with confocal fluorescence microscopy and UV LA ICP MS.

91 the dye barrier, were assessed by time-lapse confocal, fluorescence microscopy and by electron micros

92 We used TEM, confocal fluorescence microscopy, and a novel correlativ

93 attering, differential scanning calorimetry, confocal fluorescence microscopy, and atomic force micro

94 a combination of yeast two-hybrid analysis, confocal fluorescence microscopy, and fluorescence reson

95 ex vivo MRI, x-ray fluorescence microscopy, confocal fluorescence microscopy, and histological analy

96 llography, isothermal titration calorimetry, confocal fluorescence microscopy, and in vivo photoactiv

97 monstrated using atomic force microscopy and confocal fluorescence microscopy, and possible explanati

98 imultaneous confocal reflectance microscopy, confocal fluorescence microscopy, and rheology.

99 trated by nanopore formation experiments and confocal fluorescence microscopy, and they can act as co

100 Here, we describe a confocal fluorescence microscopy-based analytical method

101 A confocal fluorescence microscopy-based assay was used fo

102 ed that we could indeed realize multichannel confocal fluorescence microscopy by utilizing the freque

103 ndocytosis (RME) based on flow cytometry and confocal fluorescence microscopy (CFM) analyses, which e

104 rmation reported by the two techniques, with confocal fluorescence microscopy (CFM) used to supplemen

105 confocal reflectance microscopy (CRM) and/or confocal fluorescence microscopy (CFM).

106 ECs) using atomic force microscopy (AFM) and confocal fluorescence microscopy (CFM).

107 ith confocal reflection microscopy (CRM) and confocal fluorescence microscopy (CFM).

108 Confocal fluorescence microscopy combined with internal

109 Using single-molecule confocal fluorescence microscopy combined with optical t

110 We used confocal fluorescence microscopy correlated with scannin

111 Confocal fluorescence microscopy demonstrated that MIP i

112 a complex with IL-13Ralpha1 in solution, and confocal fluorescence microscopy demonstrated that these

113 Confocal fluorescence microscopy demonstrated that, for

114 Rather, confocal fluorescence microscopy demonstrated the loss o

115 Further, confocal fluorescence microscopy demonstrates that C. ko

116 Confocal fluorescence microscopy demonstrates that Fre6:

117 Confocal fluorescence microscopy demonstrates that Slob

118 h a combination of three imaging modalities: confocal fluorescence microscopy, direct stochastic opti

119 n using both stimulated Raman scattering and confocal fluorescence microscopy established rhabduscin'

120 after magnetic field exposure using fibered confocal fluorescence microscopy (FCFM).

121 Confocal fluorescence microscopy has established the uti

122 Fluorescence lifetime measurements and confocal fluorescence microscopy have been applied to ob

123 The method combines confocal-fluorescence-microscopy image stacks of giant u

124 Moreover, confocal fluorescence microscopy images of HeLa cells sh

125 s successfully been used to stain and record confocal fluorescence microscopy images of HeLa cells.

126 Confocal fluorescence microscopy images of the perpendic

127 s of 5-D (x,y,z,t,channel) and large montage confocal fluorescence microscopy images.

128 We then used flow cytometry and live cell confocal fluorescence microscopy imaging to show that ul

129 cation as stains of vesicle substructures in confocal fluorescence microscopy imaging.

130 Confocal fluorescence microscopy, immunocytochemistry an

131 s treated with PAI-1 were subjected to laser confocal fluorescence microscopy, immunoprecipitation an

132 fluorescent tag, was prepared and studied by confocal fluorescence microscopy in human lung adenocarc

133 f tagging with green fluorescent protein and confocal fluorescence microscopy in live cells of the cy

134 We also utilized confocal fluorescence microscopy in mapped whole mount c

135 more mitochondrial localization as shown by confocal fluorescence microscopy in OVCAR-5 cells, and,

136 e distribution as scored by conventional and confocal fluorescence microscopy in response to an ER ex

137 bution in the liver, they were detectable by confocal fluorescence microscopy in tumor-free tissue an

138 ion of electron microscopy and hyperspectral confocal fluorescence microscopy in wild-type Synechocys

139 fluorescence resonance energy transfer, and confocal fluorescence microscopy) in combination with Mo

140 ng studies against Bacillus subtilis through confocal fluorescence microscopy indicated that Cu NCs s

141 llular bacterial trafficking was followed by confocal fluorescence microscopy, intracellular bacteria

142 A detailed and systematic polarized confocal fluorescence microscopy investigation is presen

143 Confocal fluorescence microscopy is a powerful biologica

144 lular Zn(II) of eukaryotic cells using laser confocal fluorescence microscopy is demonstrated.

145 Confocal fluorescence microscopy is often used in brain

146 the utility of the extended FMDV 2A system, confocal fluorescence microscopy is used to demonstrate

147 In this part 3, a third modality, confocal fluorescence microscopy, is added to the techni

148 s of NCAMs were studied using laser scanning confocal fluorescence microscopy (LSCFM).

149 -driven reporter gene expression by in vitro confocal fluorescence microscopy, luciferase assay, 2'-f

150 Confocal fluorescence microscopy of Ad-infected NM showe

151 nylated UTP nick end labeling (TUNEL) stain, confocal fluorescence microscopy of ethidium bromide-sta

152 Confocal fluorescence microscopy of giant unilamellar ve

153 Differential scanning calorimetry and confocal fluorescence microscopy of giant unilamellar ve

154 Confocal fluorescence microscopy of live and fixed HT22

155 escence-activated cell sorting analysis, and confocal fluorescence microscopy of live cancer cells, l

156 Confocal fluorescence microscopy of thin-sectioned lymph

157 Confocal fluorescence microscopy of tumor cells incubate

158 e these arrays with high-resolution scanning confocal fluorescence microscopy on the Si-face, observi

159 d biochemical changes in the same cell using confocal fluorescence microscopy or STED.

160 By confocal fluorescence microscopy, p85alpha was shown to

161 By using quantitative confocal fluorescence microscopy, PLF could be scored on

162 Confocal fluorescence microscopy proved integrin-mediate

163 2D and 3D catalyst screening via confocal fluorescence microscopy represents an accessibl

164 Live-cell confocal fluorescence microscopy revealed both filamento

165 ges of virus-infected, OVA-treated mice, and confocal fluorescence microscopy revealed colocalization

166 Analysis by confocal fluorescence microscopy revealed single-step ph

167 , II, or III InsP3 receptors and analyzed by confocal fluorescence microscopy revealed that all InsP3

168 Confocal fluorescence microscopy revealed that HIV-1 pro

169 Confocal fluorescence microscopy revealed that internali

170 Subcellular fractionation and confocal fluorescence microscopy revealed that little or

171 Confocal fluorescence microscopy revealed that Streptaph

172 Conventional fluorescence microscopy and confocal fluorescence microscopy revealed that the bacil

173 Confocal fluorescence microscopy revealed that the BMV 1

174 Confocal fluorescence microscopy reveals cell-specific a

175 Confocal fluorescence microscopy reveals the accumulatio

176 Furthermore, confocal fluorescence microscopy showed altered localiza

177 damine-conjugated phalloidin and analysis by confocal fluorescence microscopy showed disruption of th

178 Confocal fluorescence microscopy showed that a fraction

179 Confocal fluorescence microscopy showed that both NCoR a

180 Confocal fluorescence microscopy showed that P. aerugino

181 Confocal fluorescence microscopy showed that Tyr(P)992 r

182 Confocal fluorescence microscopy shows a regime of coexi

183 Confocal fluorescence microscopy shows colocalization of

184 atment fluorescent labeling of 1 observed by confocal fluorescence microscopy shows nuclear and inten

185 Confocal fluorescence microscopy shows that the 6-micron

186 s in a dose-dependent manner, as revealed by confocal fluorescence microscopy, signaling pathways, mo

187 Confocal fluorescence microscopy studies demonstrated th

188 Confocal fluorescence microscopy studies of human skin p

189 Confocal fluorescence microscopy studies revealed that t

190 Proximity labeling and confocal fluorescence microscopy studies showed that CD5

191 inus ends were recorded with a spinning-disk confocal fluorescence microscopy system.

192 onsistent with a subsequent observation from confocal fluorescence microscopy that aggregates concent

193 We then show with confocal fluorescence microscopy that incubation of CD4+

194 phospholipids, we found, by conventional and confocal fluorescence microscopy, that transport of wate

195 pection of single EV with high confidence by confocal fluorescence microscopy, thus enables colocaliz

196 ayers Percent of ablation was determined via confocal fluorescence microscopy to be approximately 70%

197 We employed pulse field gradient NMR and confocal fluorescence microscopy to determine membrane a

198 We used confocal fluorescence microscopy to image the distributi

199 In this work, we have used wide-field and confocal fluorescence microscopy to investigate the spat

200 ring molecular motion in vitro, coupled with confocal fluorescence microscopy to measure the movement

201 We have undertaken confocal fluorescence microscopy to monitor P-bodies in

202 cytes by using scanning and stationary-point confocal fluorescence microscopy to record Ca2+ signals

203 cattering (CARS) microscopy multiplexed with confocal fluorescence microscopy to spatially map LDs an

204 y we used perforated patch voltage clamp and confocal fluorescence microscopy to study the contributi

205 result, we employed real-time analysis using confocal fluorescence microscopy to study the spatio-tem

206 tographic stationary phase with quantitative confocal fluorescence microscopy under real reversed-pha

207 The reactions were observed in real time by confocal fluorescence microscopy using a Bodipy fluoroge

208 m of infected cells was analyzed by scanning confocal fluorescence microscopy using a newly developed

209 CD205, mPDCA, B220, and GR1) and analyzed by confocal fluorescence microscopy using emission fingerpr

210 l autoradiography, immunohistochemistry, and confocal fluorescence microscopy using human brain speci

211 nal and imaging flow cytometry as well as in confocal fluorescence microscopy using overexpressing an

212 Confocal fluorescence microscopy was employed to capture

213 Confocal fluorescence microscopy was used to examine co-

214 graphy to delineate nerve fiber tracts while confocal fluorescence microscopy was used to image cell

215 Single molecule confocal fluorescence microscopy was used to perform pho

216 Time-resolved three-dimensional confocal fluorescence microscopy was used to study insul

217 Using confocal fluorescence microscopy, we compared tubulin bi

218 Using combined atomic force and confocal fluorescence microscopy, we demonstrate that th

219 Combining optical traps and confocal fluorescence microscopy, we determine here the

220 Interestingly, by immunoblotting and confocal fluorescence microscopy, we disclosed a robust

221 Using confocal fluorescence microscopy, we find that Gab2 is r

222 ceptor-green fluorescent protein chimera and confocal fluorescence microscopy, we found that NF-M red

223 emical assays, reporter gene expression, and confocal fluorescence microscopy, we investigated whethe

224 Using C2C12 cells and confocal fluorescence microscopy, we showed that MyoD an

225 Using confocal fluorescence microscopy, we visualized small en

226 Using time-lapse confocal fluorescence microscopy, we were able to visual

227 siRNAs, co-immunoprecipitation, and confocal fluorescence microscopy were employed to identi

228 cence imaging, histological examination, and confocal fluorescence microscopy were used to identify e

229 -of-the-art 3D TFM methods typically rely on confocal fluorescence microscopy, which can impose limit

230 vide a planar geometry readily accessible by confocal fluorescence microscopy, which enabled us for t

231 aring our estimates with data obtained using confocal fluorescence microscopy, which represents the f

232 tion by immuno-labeling using laser scanning confocal fluorescence microscopy, which revealed an ICI-

233 C1-INH and TagA on the bacterial surface by confocal fluorescence microscopy, which ultimately resul

234 In this study, we used spinning-disk confocal fluorescence microscopy with high temporal and

235 oline (DLPC/DPPC)/cholesterol were imaged by confocal fluorescence microscopy with two fluorescent pr

236 e-contrast microscopy and time-lapse digital confocal-fluorescence microscopy with fluorescent DiI-LD

237 tool, in conjunction with more conventional confocal fluorescence microscopy, with which to image mi

238 ivo was estimated by MRI at 7 Tesla, ex vivo confocal fluorescence microscopy, x-ray fluorescence mic