ライフサイエンスコーパス: microplate

1 roteasome activity in the nonbinding surface microplate.

2 d sample type are important when selecting a microplate.

3 de and elution, is less than 1 h per 96-well microplate.

4 more that is attached to the former Monterey microplate.

5 on of the northern boundary of the Galapagos microplate.

6 e, north of the clockwise-rotating Galapagos microplate.

7 cyclase (sGC) activity adapted for a 96-well microplate.

8 nd sensitivity was developed using a 96-well microplate.

9 ed by its gelation in 384-well RWG biosensor microplates.

10 ntional analytical laboratory microtubes and microplates.

11 heart and liver samples when using different microplates.

12 escent tags from peptide substrates in black microplates.

13 till attached to the Guadalupe and Magdalena microplates.

14 ount by protein antibody in the same well of microplates.

15 zation of 95 substrates by use of Biolog GP2 MicroPlates.

16 eous shearing of samples in standard 96-well microplates.

17 er plate technology to create microarrays in microplates.

18 and on two other cancer cell lines sorted in microplates.

19 formed both in separate cells and in 96-well microplates.

20 ) monoclonal antibody immobilized on 96-well microplates.

21 ymer layer to the polystyrene surface of the microplates.

22 robotic substrate quantification in 24-well microplates.

23 graphite in the form of nanoribbons (1D) or microplates (2D) of a few nm in thickness.

24 9 pure lipophilic compounds was examined by microplate-ABTS and HPLC-ABTS, using similar experimenta

25 ed in tomato and peppers were measured using microplate-ABTS and HPLC-ABTS.

26 onoclonal antibody against F(1) in a 96-well microplate activity assay system, to establish a method

27 e NO metabolites, nitrite, and nitrate, in a microplate adaptation of the Griess assay.

28 This protocol describes a microplate-adapted colorimetric ascorbate assay, in whic

29 We describe a microplate-adapted colorimetric total phenolics assay th

30 A new microplate-adapted DPPH rapid assay was developed to ass

31 tained by indirect colorimetric methods: the microplate Alamar Blue assay (MABA) and the tetrazolium

32 mide exhibited antimicrobial activity in the microplate alamarBlue assay (MABA) and low oxygen recove

33 sp.-(f)Si NP was immobilized on the wells of microplate and associated directly with the optical tran

34 The assay is performed in a microplate and is assessed with a 96-well multi-detectio

35 The integration of microplate and microarray methods for crude cell lysates

36 transmit the drag of the major plates to the microplate and of the mechanically weaker mobile belts s

37 ults in covalent attachment of biotin to the microplate and provides a colorimetric output upon conju

38 e enables its full implementation in plastic microplates and efficient application for routine analys

39 ed arrays on the crystalline faces of the FF microplates and that surface roughness significantly cha

40 based on the fluorescent properties of white microplates and the ability of a colored product to quen

41 fficiency assessment method based on 96-well microplates and UV-vis spectroscopy.

42 opaque and birefringent substrates, cells in microplates, and bulk tissues.

43 itochondria attached to XF24 V7 cell culture microplates, and by comparison to classical Clark electr

44 g and upconversion microspheres, crystalline microplates, and color-barcoded microrods, as well as qu

45 ubes or formed the top of V-bottom multiwell microplates, and fluid was collected in the bottom of th

46 architectures to guide formation of fibers, microplates, and micro-flowers.

47 ance after passive adsorption to polystyrene microplates, and this restricts the full use of double n

48 erm cultured live primary neurons in 96 well microplates, and uses automatic image analysis to quanti

49 , a filtration-based assay that uses 96-well microplates, and which has important application in in v

50 have been synthesized from well-defined SnO microplates ( approximately 2.0 mum) using focused solar

51 on limits in the pM range and polymer-coated microplates are stable to storage at room temperature fo

52 al 96 and 192 well polyacrylamide or agarose microplate array diagonal gel electrophoresis (MADGE) wh

53 ed DNA products (n = 80) are resolved by one microplate array diagonal gel electrophoresis using 5% p

54 Tetra-primer ARMS-PCR was combined with microplate array diagonal gel electrophoresis, gaining t

55 Microplates arrayed with 156 Chlamydia trachomatis fusio

56 ImmunoCard STAT! and the ProSpecT Giardia EZ microplate assay (Alexon-Trend, Inc.) were 81 and 91%, r

57 munoCard STAT!, the ProSpecT Cryptosporidium microplate assay (Alexon-Trend, Inc.), and modified Kiny

58 Alamar Blue assay (MABA) and the tetrazolium microplate assay (TEMA) (agreement, 95, 98, and 94%; kap

59 RNase A rather than fluorescein-RNase A in a microplate assay at pH 7.12 increased the Z'-factor from

60 icroplate assay for Giardia and the ProSpecT microplate assay for Cryptosporidium, and modified Kinyo

61 rescent-antibody (DFA) test, the ProSpecT EZ microplate assay for Giardia and the ProSpecT microplate

62 Using a novel real-time kinetic microplate assay for GTPCH activity and purified prokary

63 lly available ProSpecT Entamoeba histolytica microplate assay from Remel and the E. histolytica II en

64 ds that enables the development of a 96-well microplate assay in both enzyme- and cell-based formats

65 Enzyme activity measured in the microplate assay is comparable to values measured by usi

66 The biosensor microplate assay offered accurate "hands-off" evaluation

67 tected by the ImmunoCard STAT!, the ProSpecT microplate assay or modified Kinyoun's acid-fast stained

68 A fluorescence polarization (FP) microplate assay suitable for screening compounds agains

69 ime and applied as a label in bioluminescent microplate assay to detect target antibodies.

70 ng a high throughput fluorescence anisotropy microplate assay to identify small molecule inhibitors o

71 r recently described fluorescence anisotropy microplate assay to investigate binding and dissociation

72 In this report we describe a microplate assay to study GCPII inhibition that is most

73 ansduction in cultured cells, we developed a microplate assay using a fluorescence/luminescence plate

74 A high-throughput microplate assay was developed that uses Nile red dye to

75 A fluorescence-based microplate assay was developed to quantify cell death ba

76 Compared to the ProSpecT microplate assay, the E. histolytica Quik Chek (Quik Che

77 rapid than the previously reported standard microplate assay.

78 idermoid carcinoma cells was quantified in a microplate assay.

79 We report a label-free "microarray-in-microplate" assay platform for simultaneous acquisition

80 In this study, single-cell microplate assays were performed to measure the viscoela

81 s corresponding to the reduction observed in microplate assays.

82 The applicability of the microplate-based antioxidant assay for high-resolution s

83 This work describes the coupling of a microplate-based antioxidant assay with a hyphenated sys

84 Here we describe a microplate-based assay for discovery of VEGF-C/Nrp2 inhi

85 as a substrate, we have developed a 96-well microplate-based assay that can be conveniently used for

86 oated on plastic plates was established by a microplate-based assay using Eu(3+)-labeled proteins and

87 A microplate-based assay was developed for high-throughput

88 atomic-force microscopy and to an equivalent microplate-based assay, providing independent evidence f

89 Microplate-based assays have been implemented for thirte

90 ients of variation are comparable with other microplate-based assays.

91 nd to simplify the assay we have developed a microplate-based ChIP (Matrix ChIP) method, where all st

92 We have previously introduced a microplate-based ChIP platform, Matrix ChIP, where the e

93 In this work we present a simple microplate-based colorimetric assay for H2S gas.

94 Eschewing microplate-based compound collections for one-bead-one-c

95 Spot-based assays are advantageous for microplate-based detection for reducing the time require

96 ation reactions that enhance the accuracy of microplate-based detection of amino acids.

97 ly using a microcolumn-based device, MEDUSA (Microplate-based Enrichment Device Used for the Selectio

98 We analyzed suitability of the microplate-based FA assay for high-throughput screening

99 We developed a rapid microplate-based fluorescence anisotropy (FA)/fluorescen

100 a similar lower detection threshold for the microplate-based fluorescent detection assay of secreted

101 We developed a microplate-based fluorometric method for the concurrent

102 However, microplate-based FRAP (mFRAP) assays are affected by sam

103 It was found that the microplate-based high-resolution antioxidant assay is an

104 The developed microplate-based immunoassay allows detection of two pro

105 A 96-well-microplate-based ion flux method utilizing readily avail

106 This new microplate-based method represents a fast, inexpensive a

107 h GOD and based on this observation, a novel microplate-based method was developed to assess alpha-am

108 e in agreement with those obtained using the microplate-based method.

109 In microplate-based multiplex experiments, such as Luminex

110 We describe here a set of microplate-based oligonucleotide assays for high-through

111 A microplate-based respirometry apparatus was used.

112 Microplate-based separation assays were performed in Pac

113 The Victoria microplate between the Eastern and Western Branches of t

114 sly developed Sphingomonas sp. based optical microplate biosensor for methyl parathion (MP) was good

115 n equivalent to the same assay in a 384-well microplate but in a 64-fold smaller reaction volume, a 2

116 biopsies and individually deposited into PCR microplates by flow sorting.

117 ttle as 0.5 ng of DNA per well and a 96-well microplate can be analysed in 12 min providing an attrac

118 We envisage that this simple POC hybrid microplate can have broad applications in various bioass

119 However, even with microplate ChIP assays, sample preparation and chromatin

120 subducting oceanic slab detached from these microplates close to the trench, but recent seismic tomo

121 Microplates coated with Histoplasma antigen were used fo

122 liquots of starting library, and its 96-well microplate compatibility to enable the continued use of

123 iagonal gel electrophoresis (MADGE) which is microplate compatible and suitable for PCR checking, SNP

124 This microplate-compatible method is sensitive to the charge

125 e spectrophotometric characterization of the microplate containing dried or fresh DPPH free radicals

126 in contact with the underside of a 384-well microplate containing flat-bottomed semiconical wells.

127 The underside of a 96-well microplate cover was coated with Nafion polymer doped wi

128 Here, we manufactured a novel 96-well microplate device specifically designed to extract plasm

129 reated as rigid blocks driven by drag on the microplates' edges3.

130 th detection limits similar to or lower than microplate ELISAs at 25% assay cost and time.

131 application that provides randomization for microplate experiments, ensuring that the main principle

132 0 microl volume to allow the use of 384-well microplates, facilitating high-throughput screening of c

133 to unipolar p-type behavior in CH3 NH3 PbI3 microplate field-effect transistors by thermal annealing

134 nalysis (P < 0.01) suggesting that our novel microplate fluorescence method could be applied for the

135 A more sensitive microplate fluorescent assay was developed by monitoring

136 By using the microplate fluorimeter protocol, 96 cultures can be meas

137 dating to be an alternative to 96-well ELISA microplate for food safety monitoring.

138 ly(methyl methacrylate)) hybrid microfluidic microplate for low-cost, high throughput, and point-of-c

139 ied and optimized this method to use 96-well microplates for high throughput, to gain greater sensiti

140 size to be reduced by 5- to 10-fold, and the microplate format allows a significant increase in throu

141 This assay is compatible with a 384-well microplate format and sensitive, satisfies statistical c

142 The assay is optimised for a 96-well microplate format and spectrofluorimetric quantification

143 /Rep-Feo replicon cell line for the 384-well microplate format and used this line to screen a large l

144 We have developed a fluorescent semi-microplate format assay of protein carbonyls involving d

145 ternative platform to perform bioassays in a microplate format that exploits evaporation to drive ass

146 The assay also performed well in a 384-well microplate format under initial rate conditions (10% con

147 The method has been developed in a microplate format using an automatic reader, reaching a

148 The hybridization assay was developed in a microplate format with a total assay time of 1.5 h and w

149 ily Heart Study was assayed using a reliable microplate format with three substrates: paraoxon, pheny

150 e DNA hybridization assay was developed in a microplate format without the need for sample PCR amplif

151 ively quick and can be performed entirely in microplate format, allowing for the processing of dozens

152 d, as we demonstrate via miniaturization for microplate format, amenable for screening of compounds o

153 HTS was carried out in 384-well microplate format, and the signal-to-background ratio an

154 By using a 96-well microplate format, our method provides a flexible and ef

155 y and may be the better choice for assays in microplate format, where a short measurement time is req

156 power (FRAP) assay was recently adapted to a microplate format.

157 ng, and washing conditions were optimized in microplate format.

158 based assay for RNR activity measurements in microplate format.

159 e to high-throughput screening in a 384-well microplate format.

160 on change at 412nm through recording using a microplate format.

161 les with high throughput by using a 384-well microplate format.

162 of SOD activity in crude leaf extracts in a microplate format.

163 fectively for high-throughput screens in the microplate format.

164 d GC-rich DNA template under a novel 96-well microplate format.

165 bricate glucose microbiosensors in a 96-well microplate format: (1) the biosensor ink was dip-coated

166 n developed for use in both 96- and 384-well microplate formats and was validated using a known bisub

167 of these multiplexed assays in conventional microplate formats is considerably expensive due to the

168 y readily applicable to 96-well and 384-well microplate formats with robotic operation was developed

169 ysis and can be adapted for 96- and 384-well microplate formats.

170 table for implementation in 96- and 384-well microplate formats.

171 Some of the microplate fragments ceased subducting before the spread

172 alyses of the organic microrings and organic microplates from T. pseudonana.

173 roximately 25% faster than in a conventional microplate, further validate the diagnostic performance

174 This microplate gel-filtration method was optimized in studie

175 technology is based on graphene oxide-coated microplates (GOMs) and photoluminescent bioprobes (PLBs)

176 uction of the Indian plate beneath the Burma microplate has been released, and there is no immediate

177 ts, which immobilized on streptavidin-coated microplate, hybridized with biotinylated capture probes.

178 munofluorescence microscopy, immunoblot, and microplate immunoassay are essentially not in situ and r

179 The four rapid tests were a microplate immunoglobulin M (IgM)-enzyme-linked immunoso

180 solutes have been determined in one 96-well microplate in 4 h.

181 nual transfer from PCR or other reactions in microplates, into 768 or 384 well gels.

182 tible with industry standard 96 and 384 well microplates is commonplace.

183 In microplate luminometer format, mixtures containing 1.0 f

184 emits luminescence that can be measured by a microplate luminometer.

185 ed with good efficacy on maleimide-activated microplates (MAM) and gold electrodes.

186 y through the polystyrene commonly used as a microplate material.

187 ates indicates that the two counter-rotating microplates may be treated as rigid blocks driven by dra

188 iciently excite several vibration modes of a microplate MEMS resonator and the fundamental mode of a

189 The kinetic microplate method described here determines the minimum

190 The present study describes the rapid microplate method to determine pyruvic acid content in d

191 nitrate reductase assay and (ii) a resazurin microplate method.

192 Our kinematic solution for microplate motion relative to the major plates indicates

193 Here, shape-defined PLGA microPlates (muPLs) were realized for the sustained rele

194 The 'incipient rift' then bounds a second microplate, north of the clockwise-rotating Galapagos mi

195 Precipitated blue black microplates of SnO are finally transformed into high ban

196 Respirometry using modified cell culture microplates offers an increase in throughput and a decre

197 ift System is one of the largest continental microplates on Earth.

198 Contrarily to other TIE methods, no microplates or stirring was required, opening possibilit

199 Ocean, thus consists of two counter-rotating microplates partly separated by the Hess Deep rift.

200 We have developed a simple microplate permethylation method that relies upon solid

201 rate a high-throughput assay using a 96-well microplate platform to measure critical coagulation conc

202 lysis, and deglycosylation steps in 96-well microplates prior to capillary Western analysis.

203 ly small crustal blocks, analogous to modern microplates, progressively amalgamated to form larger co

204 ence with different properties show that the microplate properties significantly affect the measured

205 hput and a workflow compatible with standard microplate protocols.

206 re detectable in whole cells by fluorescence microplate reader analysis, live-cell fluorescence micro

207 The spectrophotometric/microplate reader assay method for glutathione (GSH) inv

208 n cells in a 96-well plate on a fluorescence microplate reader at lambda(ex) = 430 nm and lambda(em)

209 ass microfluidic channels using a commercial microplate reader based on this principle, yielding dete

210 o-assay was developed and validated, using a microplate reader in 96-well format, C(11)-BODIPY(581/59

211 Here we describe a rapid assay in which a microplate reader is used to detect fluorescence produce

212 e sensing mechanism was first validated by a microplate reader method and then applied to the microfl

213 Equipped with a microplate reader or a microscope, the nanotoxicity assa

214 Implemented on a microplate reader platform, the FDL-based approach enabl

215 This platform incorporates a fluorescence microplate reader that allows xyz-dimensional detection

216 chnique based on resazurin reduction using a microplate reader was developed and applied for the dete

217 The custom-built cavity enhanced microplate reader was used to make measurements on a com

218 Fluorescent imaging and a microplate reader were used for cellular detection to de

219 s of hydroperoxides and carboxylic acids (by microplate reader) in samples from 24 inhibited autoxida

220 on of the enzyme conjugate was measured by a microplate reader, and the signal was inversely proporti

221 data obtained using a commercially available microplate reader, demonstrate its suitability to high-c

222 Coupled with microplate reader, this GNR nanoarray chip can potential

223 This microplate reader-based mCherry fluorescence detection m

224 o suitably position the microchannels in the microplate reader.

225 raviolet (UV) absorbance measurement using a microplate reader.

226 compared with gold standard commercial ELISA microplate reader.

227 dynamic light scattering (DLS) system with a microplate reader.

228 akes it possible to conduct assays without a microplate reader.

229 a color change that can be quantified with a microplate reader.

230 methylumbelliferyl phosphate (DiFMUP)-with a microplate reader.

231 ated directly with the optical transducer of microplate reader.

232 of up to 115-fold compared to a conventional microplate reader.

233 y compared to measurements in a conventional microplate reader.

234 sample cells and thus cannot be performed in microplate-reader format.

235 ate compounds targeting cell metabolism in a microplate-reader-based assay, along with in vivo fluore

236 riety of formats, and easily integrated with microplate readers and statistical analysis software.

237 hese plates are compatible with conventional microplate readers for quantitative absorbance and fluor

238 -NASBA chips that are compatible with common microplate readers in laboratories.

239 sed, and a highly reproducible procedure for microplate readers redeveloped.

240 at has been encountered in measurements with microplate readers, and facilitates the screening of a l

241 The microplate-receptor binding assay allowed rapid detectio

242 To address the low selectivity of the microplate-receptor binding assay, the cyclic imine neur

243 tration assay (DFA), using a set of filtered microplates, requires sub-milligram quantities of purifi

244 Catabolome analysis with Biolog GN2 microplates revealed an enhanced ability of both E. coli

245 lithospheric heterogeneities in continental microplate rotation.

246 al; and batch effects - different individual microplate runs - can be easily estimated and eliminated

247 with a detection limit of 1.2 muM of PA on a microplate scale, thus allowing measurement of the PLD-c

248 and continuous PA determination method on a microplate scale.

249 The new microplate screen identified a broader set of mutations

250 combination) and a versatile high-throughput microplate screen.

251 developed based on thin-film interference of microplates self-assembled from super-paramagnetic nanoc

252 The nanoLCA-microplate sensing platform is readily scalable to 384-

253 in resource-limited environments, expensive microplate spectrophotometers that are used in many cent

254 During the solid-state photodecomposition of microplates, spherical SnO2 nanoparticles along with tin

255 cellular structure by stacking cell-attached microplate structures with specific configurations withi

256 ecific binding of antibodies to VLPs and the microplate surface, whereas the addition of PVP-360 incr

257 With this microplate system an ATP hydrolysis assay of complex V c

258 enonis is glycerol positive in the Biolog AN Microplate system.

259 tion of proline in wines thanks to a 96-well microplate technique.

260 The microplate that gave the highest reading of trypsin-like

261 an permethylation protocol, based on 96-well microplates, that has been developed into a kit suitable

262 n meshworks, organic microrings, and organic microplates, the latter being described in the present s

263 e split aptamer fragment is immobilized on a microplate, then a test sample is added containing the s

264 ere attached to form the bottom of multiwell microplates, thereby enabling in situ analysis.

265 ansition temperature decreases with reducing microplate thickness.

266 microbelts, few-layered nanosheets, nano- or microplates, thin films, single crystals, and polycrysta

267 , as an endpoint assay performed on standard microplates, this method should enable parallel testing

268 In this paper, DPPH was dried into 96 well microplate to produce DPPH dry reagent array plate, base

269 have been cultured in 96-well scintillating microplates to develop a homogenous screening assay for

270 thermal imaging was combined with disposable microplates to perform enthalpimetric analysis using an

271 A system of ITI was combined with disposable microplates to perform enthalpimetric analysis, which wa

272 aluation; and (iii) screened with targets in microplates to provide IC(50) or K(d) values.

273 In these microplates uptake of [14C]glycine was time dependent an

274 -4-methylcoumarin (AMC) were affected by the microplate used.

275 , high-throughput LPS detection in a 96-well microplate using a transcriptional biosensor system, bas

276 rd, white, low-volume 384-well and 1536-well microplates using a fluorometric plate reader for detect

277 f free-standing super-paramagnetic thin-film microplates using external magnetic fields.

278 The assay was performed in 96-well microplates using membrane preparations from rat liver a

279 ocated in Pennsylvania were evaluated by the microplate virus isolation method, and pooled sera were

280 y to chelate Fe(2+) and Cu(2+) using 96-well microplates, we analyzed Brazilian coffees (n=20) as a s

281 or incorporated into the bottom surface of a microplate well and a microfluidic channel.

282 olatile gas, and as it is volatilized in the microplate well it reacts with Ag(+) to produce Ag2S nan

283 The aptamer was covalently immobilized on a microplate well surface to act as target capture element

284 DNA immobilized to a microplate well was treated sequentially with methyltran

285 forces and contact forces (between bead and microplate well), and was not an artifact of residual mo

286 e initiated and detected in the same tube or microplate well, so that the experiment can be scaled up

287 ic acetylcholine receptors on the surface of microplate wells and the use of biotinylated-alpha-bunga

288 Microplate wells are routinely processed at a rate of 40

289 ade of glass fiber membrane were placed into microplate wells in order to significantly lengthen the

290 pedo electrocyte membranes on the surface of microplate wells proved to be a high-throughput format f

291 le and straightforward technique for coating microplate wells with molecularly imprinted polymer nano

292 A technique for coating microplate wells with molecularly imprinted polymers (MI

293 recipitation to DNA purification are done in microplate wells without sample transfers.

294 ly synthesized peptides and immobilized onto microplate wells.

295 and neuronal PC12 cells cultured in standard microplates were stained with probes and measured on a c

296 et up user-friendly assays based on combined microplate/Western blotting techniques that specifically

297 ugal technological platforms such as 24-well microplates while offering a screening efficiency-the nu

298 g cell-based assays in high-density formats (microplates with at least 384 wells), it is becoming cle

299 Our studies of individual perovskite microplates with variable thicknesses demonstrate that t

300 rs that address samples from an open shaking microplate without any microfluidics.