ライフサイエンスコーパス: fluorescence microscope

1 led endocytic structures are examined with a fluorescence microscope.

2 astuzumab-(IRDye800)(m) and examined under a fluorescence microscope.

3 force trap (optical tweezers) on an inverted fluorescence microscope.

4 ounted on the motorized stage of an inverted fluorescence microscope.

5 Images were recorded by fluorescence microscope.

6 concentrations of Hg2+ using a conventional fluorescence microscope.

7 , and also in frozen cross-sections, under a fluorescence microscope.

8 F followed by EGF-Cy5.5 and examined under a fluorescence microscope.

9 cessed as frozen sections, and viewed with a fluorescence microscope.

10 n a custom-made observation platform under a fluorescence microscope.

11 ole dihydrochloride (DAPI) and imaged with a fluorescence microscope.

12 canning confocal microscope, and an inverted fluorescence microscope.

13 the CTIS combined with a commercial inverted fluorescence microscope.

14 ioning capability of a two-photon excitation fluorescence microscope.

15 e lens epithelial cells was monitored with a fluorescence microscope.

16 data obtained with standard filter sets in a fluorescence microscope.

17 ators and a laser scanning confocal or video fluorescence microscope.

18 dization and immunoanalysis monitored with a fluorescence microscope.

19 ecial stage and observed under an intravital fluorescence microscope.

20 re straightforward and use only a wide-field fluorescence microscope.

21 d by the negative-staining appearance in the fluorescence microscope.

22 individual counting using a smartphone-based fluorescence microscope.

23 are to assemble an automated high-resolution fluorescence microscope.

24 gle molecules in a total internal reflection fluorescence microscope.

25 , incubating, and imaging the sample using a fluorescence microscope.

26 axial and coronal images using a wide-field fluorescence microscope.

27 elium cryostat that houses a superresolution fluorescence microscope.

28 neuronal calcium waves, using a standard epi-fluorescence microscope.

29 can be easily implemented on any wide-field fluorescence microscope.

30 tion cross-flow membrane system mounted on a fluorescence microscope.

31 ellular markers and a miniature head-mounted fluorescence microscope.

32 Immunoagglutination can be observed under a fluorescence microscope.

33 y images Au(3+) in living HeLa cells under a fluorescence microscope.

34 tection is achieved using a smartphone-based fluorescence microscope.

35 obes, appearing as alternative bands under a fluorescence microscope.

36 ndividual codes identifiable using a typical fluorescence microscope.

37 isting fluorescence techniques on a standard fluorescence microscope.

38 LAMP2 and LC3 with Rab7 was observed under a fluorescence microscope.

39 ionuclide uptake by single live cells with a fluorescence microscope.

40 zation of lipofuscin-AF and NIR-AF under the fluorescence microscope.

41 zed and imaged individually using a confocal fluorescence microscope.

42 , and live cell motility GFP-tracking with a fluorescence microscope.

43 dual optical trap interlaced with a confocal fluorescence microscope.

44 s flat mounted, and images were taken with a fluorescence microscope.

45 tup for use with a widely available compound fluorescence microscope.

46 , and the microarray was imaged using an epi-fluorescence microscope.

47 f the microscope objective on a standard epi-fluorescence microscope.

48 performed in a single sample with a modified fluorescence microscope.

49 g/ml applied CTB could be observed under the fluorescence microscope.

50 he state-of-the-art emission filters used in fluorescence microscopes.

51 gets at nanoscale resolution on conventional fluorescence microscopes.

52 to be imaged in living cells using standard fluorescence microscopes.

53 h modern light emitting diode (LED)-equipped fluorescence microscopes.

54 on wide-field and total internal reflection fluorescence microscopes.

55 r existing epi- or total internal reflection fluorescence microscopes.

56 recorded with confocal and light sheet-based fluorescence microscopes.

57 s not optimized for filters commonly used in fluorescence microscopes.

58 oach can also be straightforwardly used with fluorescence microscopes.

59 Optimizing the design of a two-photon fluorescence microscope (2PFM) and sample preparation pr

60 eeds very general lab equipment, including a fluorescence microscope, a syringe pump, and a simple mi

61 introduce a compact, high-speed light-sheet fluorescence microscope achieving 850 nm isotropic resol

62 In a total internal reflection fluorescence microscope, an evanescence excitation field

63 mage volumes, gathered from a single type of fluorescence microscope, an instant Structured Illuminat

64 Fluorescence microscope analysis detected microneme and

65 Confocal fluorescence microscope analysis indicates that in COS c

66 essive movement in total internal reflection fluorescence microscope analysis, demonstrating that myo

67 on in sarcomere lengths, and only requires a fluorescence microscope and a CCD camera.

68 bserved in living samples using a wide-field fluorescence microscope and a cooled charge-coupled devi

69 amples using a custom-built smartphone-based fluorescence microscope and a paper microfluidic chip.

70 and transparent extracellular matrix using a fluorescence microscope and a simple forward data analys

71 ase-locked ultrasound lens into a two-photon fluorescence microscope and achieved microsecond-scale a

72 pe, we have developed a two-channel confocal fluorescence microscope and applied it to study the dyna

73 A custom-made smartphone-based fluorescence microscope and automated image processing a

74 chnique is easy to implement with a standard fluorescence microscope and CCD camera.

75 to a conventional total internal reflection fluorescence microscope and complements any 2D single-mo

76 rings, we built a customized single molecule fluorescence microscope and developed single particle tr

77 t using a standard total internal reflection fluorescence microscope and open-source software.

78 er simple experimental setup consisting of a fluorescence microscope and openly available trajectory

79 verall, providing both visualization under a fluorescence microscope and quantification after lysis i

80 These minicircles are visualized using fluorescence microscope and scanning electron microscope

81 forward and can be performed using a regular fluorescence microscope and standard molecular biology a

82 DNA is then quantitatively imaged with a fluorescence microscope and the fragments are sized to a

83 ning capability of the two-photon excitation fluorescence microscope and the partition and spectral p

84 ving organism by developing an image under a fluorescence microscope and useful to estimate the amoun

85 aboratory-on-a-chip applications, as typical fluorescence microscopes and charge-coupled device (CCD)

86 and single-molecule detection with standard fluorescence microscopes and inexpensive digital color c

87 nging due to the limited axial resolution of fluorescence microscopes and the heterogeneity of CME.

88 Using a confocal microscope (or fluorescence microscope) and Neurlocudia 360 digitizatio

89 at 37 degrees C on the stage of an inverted fluorescence microscope, and [Ca2+]i was measured using

90 nique is simple to implement on a commercial fluorescence microscope, and especially suitable for bio

91 ted directly from the culture dishes under a fluorescence microscope, and total DNA was then prepared

92 Miniature fluorescence microscopes are becoming an increasingly es

93 However, existing high-resolution fluorescence microscopes are physically limited by objec

94 ns of living Caenorhabditis elegans, using a fluorescence microscope-based transport assay.

95 lateral and axial resolution of a wide-field fluorescence microscope but has been too slow for live i

96 y can double the resolution of the widefield fluorescence microscope but has previously been too slow

97 f lipid bilayers can be visualized under the fluorescence microscope, but the process is very fast an

98 ows super-resolution imaging on conventional fluorescence microscopes, but has been limited to protei

99 ar radiotracers are imaged on a conventional fluorescence microscope by capturing individual flashes

100 ed sheets can be made highly visible under a fluorescence microscope by quenching the emission from a

101 detection sensitivity of a smartphone-based fluorescence microscope by using surface-enhanced fluore

102 Cost effective fluorescence microscopes can be assembled from cheaply m

103 herefore constructed a novel single-molecule fluorescence microscope capable of efficiently detecting

104 nd imaged using a total internal reflectance fluorescence microscope, cells exhibited sporadic fluore

105 ehavior in vivo and complements the existing fluorescence microscope characterization of CLIP-170 int

106 By using fluorescence microscope-charge-coupled device camera as

107 ce; detection was performed utilizing an epi-fluorescence microscope/charge coupled device imaging sy

108 th a research microscopist and by TBDx using fluorescence microscopes, classifying slides based on th

109 Existing super-resolution fluorescence microscopes compromise acquisition speed to

110 Here, we report a dual-mode fluorescence microscope configuration for bilayers forme

111 ted by the laser diode of a smartphone-based fluorescence microscope device.

112 Using an ultrafast two-photon fluorescence microscope empowered by all-optical laser s

113 the NPs with polarized light on a wide-field fluorescence microscope enabled monitoring of both prote

114 center frequency of over 150 MHz and an epi-fluorescence microscope, entitled acoustic-transfection

115 Particle diffusometry requires only a fluorescence microscope equipped with a charge-coupled d

116 n of intracellular elastase activity using a fluorescence microscope equipped with standard optics.

117 be used as an add-on module to any standard fluorescence microscope even with low NA objectives.

118 Typically implemented on a fluorescence microscope, FCS samples femtoliter volumes

119 Here we describe a compact light sheet fluorescence microscope, featuring a 45 degrees inverted

120 A hybrid photoacoustic-fluorescence microscope films oxygen-carrying blood and

121 By using a fluorescence microscope fitted with UV fluoride lenses,

122 d for visualizing myofibrils with a standard fluorescence microscope (fluorescence imaging of myofibr

123 positioning stage, and an inverted widefield fluorescence microscope (FM) on an existing FIB scanning

124 dorsal tectum with a cooled CCD camera on a fluorescence microscope for 5 to 8 hours.

125 on, we developed a dedicated single molecule fluorescence microscope for detecting single ADAMTS13 mo

126 e the adaptation of a conventional widefield fluorescence microscope for FPALM and present step-by-st

127 We test this custom designed confocal fluorescence microscope for future use with brain clarif

128 strated on a commercially available inverted fluorescence microscope frame using the method of obliqu

129 In comparison to scientific-grade fluorescence microscopes, glowscopes may have limitation

130 g distance, and large field of view confocal fluorescence microscope (H(2)L(2)-CFM) with the capabili

131 d mouse embryos acquired with three types of fluorescence microscopes, (ii) scalability by analyzing

132 apply this technique to a series of confocal fluorescence microscope image sequences of mitochondria,

133 LIF system that identifies panels containing fluorescence microscope images among figures in online j

134 Fluorescence microscope images and FT-IR spectra were us

135 Results obtained from optical fluorescence microscope images and live/dead cytotoxicit

136 Stitched fluorescence microscope images inevitably exist in vario

137 ches construct ordered restriction maps from fluorescence microscope images of individual, endonuclea

138 To verify DEP response, fluorescence microscope images were captured before and

139 Fluorescence microscope images were used to count PI-sta

140 n microscopy technique are: 1), the use of a fluorescence microscope in contrast with the confocal mi

141 tifying the theoretical resolving power of a fluorescence microscope in the condition of finite photo

142 right-green fluorescence was observed with a fluorescence microscope in virtually all examined tissue

143 We demonstrate an adaptive confocal fluorescence microscope incorporating this modal sensor

144 e fluorescence images captured by a handhold fluorescence microscope increases with increasing glucos

145 A wireless, pocket fluorescence microscope (interfaced with a smartphone) c

146 When used appropriately, a confocal fluorescence microscope is an excellent tool for making

147 ary to the well known diffraction limit, the fluorescence microscope is in principle capable of unlim

148 cept, a 0.5 numerical aperture (NA) confocal fluorescence microscope is prototyped with a 3 mm x 3 mm

149 SA that occurs inside the lens elements of a fluorescence microscope is well understood and corrected

150 to the paper channel, and a smartphone-based fluorescence microscope isolated and counted the immunoa

151 ts red-emitting state easily with a laser or fluorescence microscope lamp under conditions of low oxy

152 A novel fluorescence microscope/laser optical system was develop

153 Here we present a fluorescence microscope light path that enables imaging,

154 of focus of a digitally scanned light-sheet fluorescence microscope (LSFM), multiple image planes ca

155 a custom-made inverted confocal light-sheet fluorescence microscope (LSFM).

156 we introduce a miniature (1.9 g) integrated fluorescence microscope made from mass-producible parts,

157 bjects, then imaging them on cheap miniature fluorescence microscopes ("mini-microscopes"), it is pos

158 Miniaturized fluorescence microscopes (miniscopes) enable imaging of

159 Miniaturized fluorescence microscopes (miniscopes) have been instrume

160 CoSMoS micromirror total internal reflection fluorescence microscope (mmTIRFM).

161 Digital images from fluorescence microscope movies of living cells are fed i

162 Portable, miniaturized fluorescence microscopes now allow brain imaging in free

163 itation, having deep penetration depth, by a fluorescence microscope on a coverslip, or uptaken in a

164 ys detected by the PIXL instrument (an x-ray fluorescence microscope on the Perseverance rover) provi

165 response in Escherichia coli using standard fluorescence microscope optics for excitation at 440 +/-

166 ried out with either a trans-illuminated epi-fluorescence microscope or a fluorescence light box, bot

167 logy and cell culture reagents and a regular fluorescence microscope or flow cytometer.

168 rometric measurements on these cells using a fluorescence microscope or in cell suspension using a fl

169 missions in separate detection channels of a fluorescence microscope permit the noninvasive and ratio

170 ium response of the cells is measured with a fluorescence microscope photometry system.

171 m-sensitive fluorescent probe (fura-2) and a fluorescence microscope photometry system.

172 etermine the practical resolution limit of a fluorescence microscope, photon noise remains one essent

173 f ribonucleic acids (RNAs) on a conventional fluorescence microscope, providing information on the in

174 Fluorescence microscopes range in cost from several thou

175 Electrophysiological and fluorescence microscope recordings performed in wild-typ

176 t years, poor access to suitable light-sheet fluorescence microscopes remains a major obstacle for bi

177 The low-resolution fluorescence microscopes required are readily available

178 Images of the library under a fluorescence microscope revealed at least 40-50 differen

179 ted scanning-angle total internal reflection fluorescence microscope (SA-TIRFM).

180 A homemade spectral shift fluorescence microscope (SSFM) is coupled with a spectro

181 fiber-based time-resolved near-infrared (IR) fluorescence microscope successfully coupled lifetime di

182 calibrated single-beam optical trap within a fluorescence microscope system, one can measure forces a

183 Here, we present a light sheet fluorescence microscope that achieves 390 nm isotropic r

184 resent a simple modification to a wide-field fluorescence microscope that addresses both challenges a

185 (GFP), and then assayed processivity using a fluorescence microscope that can visualize single kinesi

186 ruction of a fully automated high-throughput fluorescence microscope that enables the imaging and cla

187 pe', a widefield, miniaturized, head-mounted fluorescence microscope that is compatible with transpar

188 d the accuracy of CellScope, a novel digital fluorescence microscope that may expand access to micros

189 These investigations became possible with a fluorescence microscope that was modified for recording

190 d science outreach classrooms with fleets of fluorescence microscopes that can engage students with h

191 Compatible with readily accessible fluorescence microscopes, these easy-to-use membrane DNA

192 Through the use of a conventional fluorescence microscope, this method demonstrates a forc

193 g-angle prism-type total internal reflection fluorescence microscope (TIRFM) was constructed and test

194 Total internal reflection fluorescence microscope (TIRFM) was used for optical ima

195 Slides were examined with a fluorescence microscope to detect the presence of male c

196 by SPORT, we constructed a dual-modality DIC/fluorescence microscope to simultaneously image fluoresc

197 Our method uses custom epi-fluorescence microscopes to automatically image single c

198 toreceptors were obtained using conventional fluorescence microscopes to image through the lens of th

199 en face in a wholemount preparation under a fluorescence microscope, to evaluate the distribution of

200 d incorporated it into two- and three-photon fluorescence microscopes, to measure and correct tissue-

201 visualized at the single-molecule level in a fluorescence microscope upon isothermal amplification an

202 Many commercial as well as custom-built fluorescence microscopes use scientific-grade cameras th

203 mplemented on a conventional reflected-light fluorescence microscope using materials and resources th

204 The multistacking was verified under a fluorescence microscope using Rhodamine 6G as the analyt

205 of intact, living tadpoles with conventional fluorescence microscopes, using the lens of the tadpole

206 e limit of detection determined with a basic fluorescence microscope was 0.006 mug l(-1) (30 pM); thi

207 In addition, a deep-ultraviolet (UV) fluorescence microscope was developed for the on-chip re

208 A smartphone-based fluorescence microscope was fabricated as a handheld in

209 A fluorescence microscope was used for assay readout in ki

210 A custom light-sheet fluorescence microscope was used for volumetric imaging

211 A confocal fluorescence microscope was used to observe the fluoresc

212 ing a digital camera attached to an inverted fluorescence microscope, we acquired images at 1 frame/s

213 built ultraviolet total internal reflection fluorescence microscope, we found that the fluorescent A

214 n of the newly developed lattice light-sheet fluorescence microscope, we reexamined their assembly dy

215 sing the sectioning effect of the two-photon fluorescence microscope, we studied the behavior of phos

216 Using a miniature fluorescence microscope, we tracked the Ca(2+) dynamics

217 lation methods for FRET quantification using fluorescence microscopes were compared.

218 ian cells was also observed under a confocal fluorescence microscope when the treated cells were expo

219 lex instrumentation like flow cytometers and fluorescence microscopes, which are both expensive and c

220 optimized a kilohertz-frame-rate two-photon fluorescence microscope with an all-optical megahertz li

221 es an open-top, single-objective light sheet fluorescence microscope with an atomic force microscope

222 molecule counting using an epi-illumination, fluorescence microscope with charge-coupled device detec

223 an inexpensive video camera and an ordinary fluorescence microscope with mercury-arc or strobed lase

224 e interface identical to that of an inverted fluorescence microscope with no additional reflection el

225 properties were obtained by using a confocal fluorescence microscope with picosecond time resolution.

226 eepDOF microscope consists of a conventional fluorescence microscope with the simple addition of an i

227 py (SIM) doubles the spatial resolution of a fluorescence microscope without requiring high laser pow

228 ion of and emission by fluorophores, the way fluorescence microscopes work, and some of the ways fluo