ライフサイエンスコーパス: microscope

1 as analyzed by conventional method (standard microscope).

2 onality can be added to an existing inverted microscope.

3 xt of the cells with a conventional confocal microscope.

4 spectrometer attached to a scanning electron microscope.

5 ing a single plane in a standard multiphoton microscope.

6 quency generation (VSFG) probe hyperspectral microscope.

7 on is similar to that of a standard confocal microscope.

8 luorescent images captured on a high-content microscope.

9 lized using a handheld fluorescence confocal microscope.

10 -field synchrotron-based extreme ultraviolet microscope.

11 wab RNA that can be read with a mobile phone microscope.

12 T and keratoplasty was commenced under i-OCT microscope.

13 e-testing device and confocal laser scanning microscope.

14 ge amenable to any standard confocal or TIRF microscope.

15 ated MLECs were observed with phase contrast microscope.

16 ectral unmixing on a laser scanning confocal microscope.

17 sion exceeding the optical resolution of the microscope.

18 ion corrected scanning transmission electron microscope.

19 ed with a TIRF-based structured illumination microscope.

20 motorized stage of an inverted fluorescence microscope.

21 etallic particles were counted under a light microscope.

22 was confirmed under confocal laser scanning microscope.

23 ment such as a heater and simple fluorescent microscope.

24 were found in red color under a fluorescent microscope.

25 lb of mouse brain, using a standard confocal microscope.

26 epifluorescence illumination and a standard microscope.

27 flow system and visualized using an inverted microscope.

28 ed to the axial point-spread function of the microscope.

29 ) directly onto the eyepiece of the surgical microscope.

30 ted onto a standard inverted epifluorescence microscope.

31 lized DNA was done using a scanning electron microscope.

32 asure bonding strength using an atomic force microscope.

33 maged at higher resolution with the confocal microscope.

34 n be imaged everywhere, every time, on every microscope.

35 ofuscin-AF and NIR-AF under the fluorescence microscope.

36 pass using a line-scanning spectral confocal microscope.

37 ctures in a (scanning) transmission electron microscope.

38 equally applicable in most single-objective microscopes.

39 organs imaged with confocal and light sheet microscopes.

40 nanoscale resolution imaging on conventional microscopes.

41 he-art emission filters used in fluorescence microscopes.

42 e-color images collected with laser scanning microscopes.

43 rom resolution were collected on Titan Krios microscopes.

44 or the builders of custom azimuthal scanning microscopes.

45 croscopes and reflective lattice light-sheet microscopes.

46 n we not see nanoscale objects under a light microscope?

47 to its high numerical aperture optics, this microscope achieves lateral and axial resolutions that a

48 Here we present a high-speed non-linear microscope achieving kilohertz frame rates by employing

49 their effect was analyzed using atomic force microscope (AFM) and scanning electron microscope (SEM)

50 Atomic force microscope (AFM) based single molecule force spectroscop

51 I implemented with a commercial atomic force microscope (AFM) is such that a dynamic range of 80 dB -

52 fingerprint when pulled with an atomic force microscope (AFM) tip.

53 iffness was also measured using atomic force microscope (AFM) to identify a possible mode of action o

54 fluorescence microscope with an atomic force microscope (AFM), providing simultaneous volumetric imag

55 A custom microscope allowed us to image the soma and up to 300 mu

56 f the point spread function in an unmodified microscope already contain rich information.

57 Electron microscope analyses suggest that the particles enriched

58 ropine in the quids, while scanning electron microscope analysis confirms most to be Datura wrightii

59 s with ex-vivo imaging via scanning confocal microscope and (ii) an improved clearing protocol compat

60 de assessments by three pathologists using a microscope and a fourth pathologist via manually ticking

61 A custom-made smartphone-based fluorescence microscope and automated image processing and particle c

62 g videos recorded using a standard slit-lamp microscope and fixed-force GAT.

63 Here, we utilize a combined atomic force microscope and light sheet microscope to show SKOV3 nucl

64 also obviates the need for a high-resolution microscope and other complex equipment, making it potent

65 In situ scanning electron microscope and transmission electron microscope testing

66 nomic and optical advantages of the surgical microscope and widefield visualisation, continuous IOP c

67 elengths are needed for both next-generation microscopes and affordable turn-key systems.

68 Here, using miniature head-mounted microscopes and cell-type-specific genetic tools, we obs

69 SerialEM controls microscopes and detectors and can trigger automated task

70 des substantial benefits when characterizing microscopes and high-resolution imaging systems in situ.

71 SRS microscopy and review innovations in SRS microscopes and imaging probes.

72 ment of ion optical devices such as electron microscopes and mass spectrometers.

73 employed with various types of conventional microscopes and permits use of both commercially availab

74 cluding dual-view cleared-tissue light-sheet microscopes and reflective lattice light-sheet microscop

75 eded are significantly cheaper than confocal microscopes and sections can be kept indefinitely.

76 near-infrared voltage indicators, high-speed microscopes and targeted gene expression schemes that en

77 from the widespread availability of confocal microscopes and the relative ease of the experiment and

78 metric bone mineral density explained 50.2% (microscope) and 49.4% (probe) of the variance in K(init)

79 STM break junction (STM = scanning tunneling microscope) and that the zero-voltage bias conductance o

80 single-molecular tracking, super-resolution microscope, and advanced quantum light sources.

81 Calberla solution, counted under an optical microscope, and converted to the number of pollen per sq

82 Place a drop of pond water under the microscope, and you will likely find an ocean of extraor

83 Beam) are routinely referred to as dual-beam microscopes, and they are equipped with a cryo-stage for

84 Such microscopes (Aquilos Cryo-FIB/Scios/Helios or CrossBeam)

85 3D models and assembly instructions of our microscope are made available for open source use.

86 Modern high-resolution microscopes are commonly used to study specimens that ha

87 However light sheet microscopes are limited by volume scanning rate and/or c

88 e intensities collected using a polarization microscope at a rate of 50 frames per second, we follow

89 a near edge X-ray absorption fine structure microscope at the National Synchrotron Light Source can

90 In this report, a full Mueller scanning microscope based on spectral encoding of polarization is

91 the form of a scale-free, vertical tracking microscope, based on a 'hydrodynamic treadmill' with no

92 I-V) characteristics in a scanning tunneling microscope-based break junction (STM-BJ) device.

93 Optical microscope-based classification and counting demands a s

94 per sample, using a traditional bright-field microscope-based flow assay allows only one sample at a

95 review introduces the state-of-the-art force microscope-based methods to map at high-spatial resoluti

96 nt of wetland flood frequency, applying both microscope-based morphological identification and DNA me

97 all vessels were (mean +/- scanning electron microscope) BD rats (40% +/- 6%), sham-operated rats (75

98 the bait, using single molecule atomic force microscope binding assays.

99 ere characterized using a scanning tunneling microscope-break junction (STM-BJ) technique, thereby en

100 m points, distant enough to be resolved by a microscope but close enough to spatially sample the rele

101 olution imaging on conventional fluorescence microscopes, but has been limited to proteins and nuclei

102 ral surgical specimens show that the DeepDOF microscope can consistently visualize nuclear morphology

103 samples with subcellular detail, the DeepDOF microscope can improve tissue sampling during intraopera

104 A SAF microscope can retrieve this near-field information thro

105 d resolution of images obtained with optical microscopes can be improved by deconvolution and computa

106 Light microscopes can now capture data in five dimensions at v

107 micrometric-sized droplet to an atomic force microscope cantilever to directly measure adhesion and f

108 In 2010, we introduced the centrifuge force microscope (CFM) as a platform for accessible and high-t

109 easibility of Intraoperative Spectral-Domain Microscope Combined/Integrated OCT Visualization during

110 easibility of Intraoperative Spectral Domain Microscope Combined/Integrated OCT Visualization During

111 However, the microscopes commonly used in pathology are limited in re

112 d the bonding interface with an atomic force microscope, conducted micro-Raman analysis, and performe

113 The DeepDOF microscope consists of a conventional fluorescence micro

114 ges of 30 different cell lines from multiple microscopes, contrast mechanisms and magnifications that

115 SLG adsorbed to a glass microscope coverslip (SLG/SiO(2)) served as a platform f

116 Our microscope design shows promise for future use in super-

117 Confocally Aligned Planar Excitation (SCAPE) microscope design that can achieve high-resolution volum

118 sis (NTA) in an off-axis digital holographic microscope (DHM) enabling determination of both particle

119 lar compartments, imaged with standard light microscopes, do not respond to other nucleotides and nuc

120 omplexes are often difficult to detect using microscopes due to their small sizes.

121 Using an ultrafast two-photon fluorescence microscope empowered by all-optical laser scanning, we i

122 Mueller microscopes enable imaging of the optical anisotropic pr

123 A custom nonlinear optical beam-scanning microscope enabled patterned illumination for photobleac

124 wt.%) were prepared using a xenon-plasma FIB microscope equipped with a cryogenic stage reaching -135

125 we describe how to prepare lamellae using a microscope equipped with both FIB and scanning electron

126 also applicable for other types of dual-beam microscopes equipped with a cryo-stage.

127 erature ultra-high vacuum scanning tunneling microscope experiment.

128 for planning unbiased and rigorous confocal microscope experiments.

129 ved by both field-emission scanning electron microscope (FE-SEM) and high-resolution transmission ele

130 rized using field emission scanning electron microscope (FE-SEM, SEM-Mapping), scanning transmission

131 Field Emission Scanning Electron Microscope (FESEM) analysis reveal surface protrusions a

132 rized using field emission scanning electron microscope (FESEM), energy dispersive X-ray spectroscopy

133 d and live cells, choosing the most suitable microscope for a given application and configuring the m

134 We developed a real-time stabilization microscope for accurate long-term, high-magnification im

135 s same material can be taken to the confocal microscope for detailed analysis at the subcellular leve

136 cs, custom software and an integrated mobile microscope for the automated culture, perfusion, medium

137 sessed in real time using an epifluorescence microscope for their migration toward the potent chemoat

138 be visualized with standard epifluorescence microscopes for high-throughput efficiency and the new s

139 647 recorded in switching buffer on the two microscopes for image superposition.

140 orm conventional diffraction-limited optical microscopes for nanoscale visualization.

141 advantage of commonly available multiphoton microscopes for the accurate positioning and orientation

142 ible to perform in a traditional light-sheet microscope geometry, including cell migration through co

143 excess solution from a transmission electron microscope grid by pressing absorbent filter paper again

144 Because optical microscopes have a limited depth-of-field (DOF), resecte

145 ic screens using high-throughput fluorescent microscopes have generated large datasets, contributing

146 However, current light-sheet microscopes have imposed constraints on the size, shape,

147 This affordable, flexible, plug-and-play microscope heralds a new era in functional imaging of fr

148 M) and high-resolution transmission electron microscope (HRTEM) images, respectively.

149 Quantification in the optical microscope identified up to 5,857 particles.L(-1) but la

150 Optical microscope images and spectrophotocolorimetry analysis e

151 ion to obtain DeSOS images from conventional microscope images obtained at low excitation powers.

152 Scanning electron microscope images of the thin-film composite membrane af

153 as embedded into knitwear, scanning electron microscope images revealed an intact nanofibrous envelop

154 Cryo-electron microscope images revealed dense prodrug-SOS complex in

155 transmission electron microscopy and optical microscope images shows that the formation of mature fib

156 al human intervention in transiting from raw microscope images to histograms of biomolecule behavior,

157 ted areas were assessed by scanning electron microscope images, chemical composition by energy disper

158 t ultrasound images, and zebrafish embryonic microscope images, with the average Dice coefficient bet

159 We used confocal microscope imaging and three-dimensional (3D) analysis t

160 Electron microscope imaging demonstrated reduced postsynaptic den

161 l cases where X-ray diffraction and electron-microscope imaging methods fail.

162 with an environmental transmission electron microscope in a novel experimental set-up.

163 ents obtained with a confocal laser scanning microscope in biofilms: 1) linear drift, 2) exponential

164 TPMDs were produced using a multiphoton microscope in Cal-520-AM loaded cells.

165 Using a miniature microscope in freely behaving mice and a two-photon micr

166 ope in freely behaving mice and a two-photon microscope in head-fixed, unanesthetized mice, we show t

167 rete frequency infrared (DFIR) spectroscopic microscopes in image quality and data throughput are cri

168 rete frequency infrared (DFIR) spectroscopic microscopes in spectral image quality and data throughpu

169 les containing images obtained with advanced microscopes include full details about how each image wa

170 sed Ion Beam combined with Scanning Electron Microscope) instrument is presented.

171 We evaluate the role of microscope-integrated intraoperative optical coherence t

172 Intraoperative microscope-integrated OCT allowed proper subretinal inje

173 observation of histopathology using optical microscope is an essential procedure for examination of

174 used appropriately, a confocal fluorescence microscope is an excellent tool for making quantitative

175 s inside the lens elements of a fluorescence microscope is well understood and corrected for.

176 les to benchmark and optimize the quality of microscopes, labels and imaging conditions.

177 plification, to directly view on a widefield microscope lambda/31-scale (25-nm radius) objects in the

178 By means of scanning tunneling microscope manipulation and imaging, the rotation steps

179 Miniaturized fluorescence microscopes (miniscopes) have been instrumental to monit

180 zoresponse force microscopy, an atomic force microscope modality that locally measures electromechani

181 Under the electron microscope, muPLs appeared as square prisms with an edge

182 It is a cost-effective approach as the microscopes needed are significantly cheaper than confoc

183 e fiber with a near-field scanning microwave microscope (NSMM) at 5-10 GHz by obtaining profiles of b

184 A custom-made microscope objective based on the supercritical angle te

185 hematic shows brain slice, patch pipette and microscope objective.

186 emission) components, can be collected with microscope objectives having a high-enough detection ape

187 ercial wide-field and spinning-disk confocal microscopes, obtaining >10-fold improvements in signal t

188 ng deep penetration depth, by a fluorescence microscope on a coverslip, or uptaken in a single HeLa c

189 s than 100 kDa using a transmission electron microscope operating at 200 keV coupled with a direct el

190 We present an oblique plane microscope (OPM) that uses a bespoke glass-tipped tertia

191 iameter measurements using custom-engineered microscope optics.

192 Here, we developed a custom three-photon microscope optimized to image a vertical column of the c

193 I(1670)/I(1640) and v(1)PO(4)/Amide I (microscope) or just I(1670)/I(1640) (probe) were negativ

194 nfrared (NIR) light provided by a two-photon microscope, or by a stand-alone laser during flow throug

195 characterizing the performance of one's own microscopes over time, allows objective benchmarking of

196 for a given application and configuring the microscope parameters.

197 roscope setup called the Photon Ion Electron microscope (PIE-scope) that enables direct and rapid iso

198 nstained breast tissue sections on a visible microscope platform.

199 However, the development of Mueller microscopes poses an instrumental challenge: the product

200 ng a fibronectin-functionalized atomic force microscope probe.

201 ueller to a Second Harmonic Generation (SHG) microscope, providing a pixel-to-pixel matching of the i

202 l information from images obtained from such microscopes remains a formidable challenge.

203 can be performed on a conventional widefield microscope, requires less illumination light to photoswi

204 ome at the expense of system complexity with microscopes routinely employing multiple objective lense

205 the net rate is 600 Mpixel per sec with six microscopes running in parallel.

206 The confocal microscope's ability to block out-of-focus light and the

207 ing algorithms are used to decrease electron microscope scan time and electron beam exposure with min

208 e in our home-built Scanning Electrochemical Microscope (SECM) setup in which an AC potential is appl

209 s for 48 hours followed by scanning electron microscope (SEM) analysis immediately or after rinsing w

210 n beam experiment inside a scanning electron microscope (SEM) chamber.

211 theoretical model based on scanning electron microscope (SEM) images of our substrates to explain our

212 force microscope (AFM) and scanning electron microscope (SEM) imaging techniques.

213 Methods such as scanning electron microscope (SEM), Fourier transform infrared spectrum (F

214 Scanning electron microscope (SEM), transmission electron microscope (TEM)

215 terization methods such as scanning electron microscope (SEM), transmission electron microscope (TEM)

216 beads was examined using a scanning electron microscope (SEM).

217 we present an integrated cryo-FIB and light microscope setup called the Photon Ion Electron microsco

218 ruli were observed in these mice under light microscope, severe proteinuria and albuminuria were foun

219 nanopipet tip of a scanning ion conductance microscope (SICM) and a conductive (working electrode) s

220 aches that put opioid drug action "under the microscope." SIGNIFICANCE STATEMENT: Opioid receptors ar

221 s approach, beads are simply dropcast onto a microscope slide and dried into a monolayer film for dig

222 a microfluidic tool compatible with standard microscope slides and cover glasses.

223 xatives, sliced into thin sections placed on microscope slides, stained, and imaged to determine whet

224 Scanning Electron Microscope (SME) was utilized to study the microstructur

225 and accuracy of single-molecule localization microscopes (SMLMs) are routinely benchmarked using simu

226 Incorporating a Scanning Probe Microscope (SPM) unit which provides topography measurem

227 conducted in scanning/transmission electron microscopes (STEM/TEM) provide a critical tool for under

228 ronic structures, using a scanning tunneling microscope (STM) combined with light irradiation at 5 K.

229 Using a scanning tunneling microscope (STM) under suitable bias conditions, binary

230 all-electric scheme in a scanning tunneling microscope (STM).

231 cles were confirmed by transmission electron microscope study.

232 The poseidon syringe pump and microscope system is an open source alternative to comme

233 re sample chamber with a two-photon scanning microscope system, allowing for the first time, to our k

234 volved studying the human brain via electron microscope techniques.

235 (AFM), High-resolution transmission electron microscope (TEM), Fourier-transform infrared spectroscop

236 tron microscope (SEM), transmission electron microscope (TEM), x-ray diffraction (XRD) method, cyclic

237 tron microscope (SEM), transmission electron microscope (TEM), x-ray diffraction (XRD), cyclic voltam

238 er NaCl on Ag(111) using scanning tunnelling microscope TERS imaging.

239 lectron microscope and transmission electron microscope testing of the smooth and rough nanoboxes sho

240 a heated chamber on an inverted fluorescent microscope that enables live-cell imaging of thermophile

241 i single-molecule switching super-resolution microscope that enables ratiometric multicolor imaging o

242 esent a multi-immersion open-top light-sheet microscope that enables simple mounting of multiple spec

243 fully automated high-throughput fluorescence microscope that enables the imaging and classification o

244 , by using a novel fluorescence polarization microscope that reports the position and the orientation

245 imaging modalities onto a standard inverted microscope that retains compatibility with microfluidics

246 udied using analytical transmission electron microscope that together with outcomes from advanced ato

247 le extension to existing objective-type TIRF microscopes that allows wide-field observations of fast-

248 ir use with images acquired from traditional microscopes that are available to virtually all fertilit

249 erformance enhancement on recently developed microscopes that have improved spatial resolution, inclu

250 imaging pipeline using transmission electron microscopes that scales this technology, implements 24/7

251 ynamics (MD) simulations as a "computational microscope" that can be used to capture detailed structu

252 ements, obtained using a scanning tunnelling microscope, that provide such evidence as a function of

253 erimental mouse brain sections under a light microscope-that of correctly identifying the distinct br

254 In the electron microscope, three major types of terminals were identifi

255 plying strain gradients with an atomic force microscope tip polarizes an ultrathin film of an archety

256 age (overpotential) against the atomic force microscope tip, generating a growth stress up to 130 MPa

257 ment of a breakthrough quantum cascade laser microscope to allow for real-time comparability assessme

258 (DLS) and confirmed by transmission electron microscope to be about 400 nm.

259 scopic technique using a scanning tunnelling microscope to detect a sequence of topological insulator

260 troscopy in a scanning transmission electron microscope to directly resolve carbon-site-specific isot

261 ivo application of a feedback-based tracking microscope to follow individual mitochondria in sensory

262 We use a miniature microscope to image the Ca(2+) dynamics within the apica

263 To determine these, we used an atomic force microscope to indent the surfaces of cultured endothelia

264 ighlight the development of the atomic force microscope to investigate interactions with glycans at t

265 Here we present a 16-beam, two-photon microscope to monitor activity across the mouse primary

266 Using scanning tunneling microscope to probe EuS islands grown on top of gold nan

267 oduce a deep-learning extended DOF (DeepDOF) microscope to quickly image large areas of freshly resec

268 We employ an ultrafast electron microscope to record movies of the subsequent electron d

269 ined atomic force microscope and light sheet microscope to show SKOV3 nuclei exhibit a two-regime for

270 Here, we use a computational microscope to show that nanocompartmentalization of IDR

271 STOMP uses a confocal microscope to visualize structures of interest and to ta

272 Interestingly, in situ cryoelectron microscope tomography has very recently shown that exact

273 velopment of single-shot ultra-fast electron microscope (UEM).

274 PATRIC and MicroScope update in microbial genomes while human and m

275 e cells in 3D, in close to real time, at the microscope using widely available and inexpensive hardwa

276 Here we used a recent electron microscope volume of the fly brain [4] to reconstruct th

277 A low-cost second harmonic generation (SHG) microscope was constructed, and, for the first time, SHG

278 retrospective group, n = 19), a conventional microscope was used during keratoplasty.

279 rated holographic optical tweezers and Raman microscope was used to investigate the effect of curvatu

280 rized measurements with a scanning tunneling microscope, we compared quasiparticle interference (QPI)

281 antages incorporated into a custom-built QCL microscope, we demonstrate a point scanning VCD instrume

282 n aberration-corrected transmission electron microscope, we report the fabrication of precious metal

283 ron energy-loss spectroscopy in the electron microscope, we show that a single substitutional silicon

284 Using this microscope, we visualized microcirculatory flow, fast ve

285 al-time, allowing the operator to adjust the microscope while constantly monitoring them.

286 igh-speed phenomena, we created a two-photon microscope with 400 illumination beams that collectively

287 stem is identical to a standard bright-field microscope with a lamp and a camera - no laser or interf

288 p, single-objective light sheet fluorescence microscope with an atomic force microscope (AFM), provid

289 Here, we extend a two-photon microscope with an electrically tunable lens allowing us

290 We combine an atomic force microscope with an environmental transmission electron m

291 Our multi-scale approach involves a microscope with an orthogonal axis design where the meso

292 prototype system that integrates a confocal microscope with an XYZ stage robot to image and automati

293 chandelier-assisted viewing at the surgical microscope with anterior chamber infusion offers the erg

294 freely behaving animals requires a portable microscope with multiple optical contrast mechanisms.

295 ment, custom surgical forceps, and operating microscope with or without intraoperative OCT (iOCT) wer

296 of vibrational spectroscopy in the electron microscope with single-atom sensitivity and has broad im

297 cope consists of a conventional fluorescence microscope with the simple addition of an inexpensive (l

298 The CFM consists of a rotating microscope with which prescribed centrifugal forces can

299 es molecular composition based on an optical microscope with wide-field interferometric detection of

300 Therefore, we developed a miniaturized microscope with: a fluorescence (FL) channel for imaging

301 Experiments were performed with a mIRage IR microscope working in a noncontact, far-field reflection