ライフサイエンスコーパス: microplate

1 more that is attached to the former Monterey microplate.

2 on of the northern boundary of the Galapagos microplate.

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

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

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

6 roteasome activity in the nonbinding surface microplate.

7 d sample type are important when selecting a microplate.

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

9 robotic substrate quantification in 24-well microplates.

10 heart and liver samples when using different microplates.

11 escent tags from peptide substrates in black microplates.

12 till attached to the Guadalupe and Magdalena microplates.

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

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

15 er plate technology to create microarrays in microplates.

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

17 ) monoclonal antibody immobilized on 96-well microplates.

18 ymer layer to the polystyrene surface of the microplates.

19 er layer onto the polystyrene surface of the microplates.

20 rations with capillary array electrophoresis microplates.

21 ated and immobilized onto neutravidin-coated microplates.

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

23 ntional analytical laboratory microtubes and microplates.

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

25 9 pure lipophilic compounds was examined by microplate-ABTS and HPLC-ABTS, using similar experimenta

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

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

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

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

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

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

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

33 easure this response in real time in 96-well microplates, allowing two people to process more than 10

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

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

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

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

38 of a radial capillary array electrophoresis microplate and scanner for high-throughput DNA analysis

39 been arrayed in individual wells of 96-well microplates and also pooled to permit rapid polymerase c

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

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

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

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

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

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

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

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

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

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

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

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

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

53 Microplate-array diagonal-gel electrophoresis (MADGE) wa

54 Microplates arrayed with 156 Chlamydia trachomatis fusio

55 erely pipetting a cell suspension into seven microplate arrays.

56 ksburg, Va.) and the Alexon ProSpecT Giardia microplate assay (Alexon, Inc., Sunnyvale, Calif.) was p

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

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

59 al culture, using the ProSpecT Campylobacter microplate assay (Alexon-Trend, Ramsey, Minn.).

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

61 enzyme immunoassays (EIAs) (ProSpecT Giardia Microplate Assay [Alexon-Trend Inc.], Giardia Test [Tech

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

63 A competitive fluorescence microplate assay based on a red-shifted green fluorescen

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

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

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

67 A microplate assay for the rapid quantitation of adenoviru

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

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

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

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

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

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

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

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

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

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

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

79 Inc. (Ramsey, Minn.), ProSpecT Campylobacter microplate assay was compared with culture on a Campy-CV

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

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

82 unit rRNA and biochemically by the BIOLOG GN MicroPlate assay, fatty acid analysis, and various stand

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

84 rapid than the previously reported standard microplate assay.

85 idermoid carcinoma cells was quantified in a microplate assay.

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

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

88 s corresponding to the reduction observed in microplate assays.

89 activity in substrate gels and quantitative microplate assays.

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

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

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

93 developed a simple, sensitive, fluorescence microplate-based assay for tumor necrosis factor (TNF) b

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

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

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

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

98 Microplate-based assays have been implemented for thirte

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

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

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

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

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

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

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

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

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

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

109 cleic acids for AP sites and mismatches in a microplate-based format.

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

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

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

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

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

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

116 A microplate-based respirometry apparatus was used.

117 Microplate-based separation assays were performed in Pac

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

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

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

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

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

123 A magnetic microplate chemifluorimmunoassay (MMCIA) is described us

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

125 Microplates coated with Histoplasma antigen were used fo

126 o adherence by oral viridans streptococci in microplates coated with whole saliva from 123 persons.

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

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

129 This microplate-compatible method is sensitive to the charge

130 The microplate consists of a central common anode reservoir

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

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

133 It was shown that the MIP-coated microplates could be used for assay development and drug

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

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

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

137 0 microl volume to allow the use of 384-well microplates, facilitating high-throughput screening of c

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

139 Utilizing a novel microplate fluorescent HAT assay which detects the enzym

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

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

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

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

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

145 This assay is adapted to a microplate format and employs glutamate oxidase and hors

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

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

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

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

150 apid, continuous assay of the enzyme using a microplate format in a fluorescence plate reader, thereb

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

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

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

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

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

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

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

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

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

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

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

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

163 based assay for RNR activity measurements in microplate format.

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

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

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

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

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

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

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

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

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

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

174 sed assays in higher density, smaller volume microplate formats.

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

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

177 Some of the microplate fragments ceased subducting before the spread

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

179 This microplate gel-filtration method was optimized in studie

180 The microplate has 96 sample wells and 48 separation channel

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

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

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

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

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

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

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

188 In microplate luminometer format, mixtures containing 1.0 f

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

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

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

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

193 The kinetic microplate method described here determines the minimum

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

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

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

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

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

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

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

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

202 inciple, the optimized fluorescamine and NDA microplate procedures reported here can be utilized as c

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

210 Because the plate is scanned in a microplate reader in only 58 s, the assay is very conven

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 rometer, filter fluorometer, or fluorescence microplate reader-surpassing the sensitivity achieved wi

225 ated directly with the optical transducer of microplate reader.

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

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

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

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

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

231 e scored by analysis of data obtained from a microplate reader.

232 y compared to measurements in a conventional microplate reader.

233 raviolet (UV) absorbance measurement using a 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 hese plates are compatible with conventional microplate readers for quantitative absorbance and fluor

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

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

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

240 The microplate-receptor binding assay allowed rapid detectio

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

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

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

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

245 and continuous PA determination method on a microplate scale.

246 The new microplate screen identified a broader set of mutations

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

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

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

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

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

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

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

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

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

256 est samples are achieved in < 120 s with the microplate system.

257 immunomagnetic separation and a fluorescent microplate technique for rapid detection of low-level Es

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

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

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

261 Using a 96-channel radial CAE microplate, the labeled ASPCR products generated from 96

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 iquid samples sequentially by sipping from a microplate through a capillary, mixes the samples with c

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

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

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

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

271 th ET primers and microfabricated radial CAE microplates to perform multiplex SNP analyses in a clini

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 A technique for coating of microplate wells with a molecularly imprinted polymer (M

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

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

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

295 ly synthesized peptides and immobilized onto microplate wells.

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

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

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.