ライフサイエンスコーパス: microtiter plate

1 n an area equivalent to a standard well of a microtiter plate.

2 erformed simultaneously in single wells of a microtiter plate.

3 nventional 9-mm pitch (spacing) of a 96-well microtiter plate.

4 a reader device with the same footprint as a microtiter plate.

5 rformed on a micromolar scale in situ in the microtiter plate.

6 ates on gold that are presented on a 96-well microtiter plate.

7 tion of both genotypes in a single well of a microtiter plate.

8 anglioside (GM1) was used for coating of the microtiter plate.

9 rate is then covalently coupled to a 96-well microtiter plate.

10 an enzyme amplification cascade in the same microtiter plate.

11 to a maleic anhydride-activated polystyrene microtiter plate.

12 in, desialylated fetuin, is immobilized on a microtiter plate.

13 ation of components in the sample wells of a microtiter plate.

14 precipitation to be carried out in a single microtiter plate.

15 implicity of CiGiP with the convenience of a microtiter plate.

16 lly through the 24 vials of a standard 6 x 4 microtiter plate.

17 Milk also removes ricin bound to the microtiter plate.

18 or copolymer are added to wells of a 96-well microtiter plate.

19 ISA) method in which Hb was immobilized on a microtiter plate.

20 ntifying CTB bound on epithelial surfaces in microtiter plates.

21 ed in rabbit plasma and on fibrinogen-coated microtiter plates.

22 analogs in assays performed in 100,000-well microtiter plates.

23 ied out in liquid medium in standard 96-well microtiter plates.

24 of in vitro biofilm formation on polystyrene microtiter plates.

25 cycloheximide-treated HEp-2 cells in 96-well microtiter plates.

26 e pools of fosmid clones arrayed in 384-well microtiter plates.

27 ped for high-throughput screening in 96-well microtiter plates.

28 ed hybrid is captured on streptavidin-coated microtiter plates.

29 which functioned as a receptacle for 96-well microtiter plates.

30 ploying native enzyme that is immobilized on microtiter plates.

31 erminal regions of both proteins in 384-well microtiter plates.

32 to high molecular weight kininogen linked to microtiter plates.

33 l binding to immobilized ligand using V-well microtiter plates.

34 ays running at low sirtuin concentrations in microtiter plates.

35 le recombinant HLA class I monomers bound to microtiter plates.

36 o-phenylenediamine (OPD) was also adapted to microtiter plates.

37 ontains 73 728 clones stored in 192 384-well microtiter plates.

38 The library is arrayed in microtiter plates.

39 nt assay (ELISA) using Hb-coated polystyrene microtiter plates.

40 nus and were attached to streptavidin-coated microtiter plates.

41 compared with static protocols performed in microtiter plates.

42 on of six histidine-containing proteins onto microtiter plates.

43 ify as few as 1000 cells per well in 96-well microtiter plates.

44 ing of trans-well contents after transfer to microtiter plates.

45 borosilicate glass surfaces and polystyrene microtiter plates.

46 t glycosidases (cellulases and xylanases) in microtiter plates.

47 of an appropriate desulphation procedure in microtiter plates.

48 ommended for high throughput desulphation in microtiter plates.

49 ubculturing visibly clear wells from the MIC microtiter plates.

50 aphic resins aliquotted in membrane-bottomed microtiter plates.

51 b, IgG, amyloid beta, and BSA immobilized on microtiter plates.

52 proximately 17 pCi/ well (or 1.6 nCi/96-well microtiter plate) 14C-1A5 was used, which is far below t

53 lutathione S-transferase fusion protein on a microtiter plate, addition of the kinase reaction mixtur

54 g the truncated gene products in an in vitro microtiter plate adherence assay.

55 e simultaneous growth of multiple strains in microtiter plates along a temperature gradient.

56 ween GCL activities measured by HPLC and NDA-microtiter plate analyses.

57 he FP assay has been formatted in a 384-well microtiter plate and automated using a pipeting workstat

58 The entire assay can be performed in a microtiter plate and is amenable to automation.

59 ample preparation device has the format of a microtiter plate and is molded in a plastic frame which

60 f APPmicroTP is also checked with respect to microtiter plate and paper-based ELISA.

61 -II) as a substrate, was coated on a 96-well microtiter plate and ST-II was in vitro transcribed and

62 rough wash device was positioned between the microtiter plate and the ESI interface.

63 es coating fibroblast growth factor (FGF) on microtiter plates and capturing fluorescein isothiocyana

64 f the obtained liposomes with the surface of microtiter plates and cartridges were investigated and 3

65 Cells were then plated in 96-well microtiter plates and exposed to varying concentrations

66 Because immobilization of proteins on microtiter plates and exposure of immobilized proteins t

67 nity for light chains immobilized on 96-well microtiter plates and for beads conjugated with a light

68 esion of human neutrophils to laminin-coated microtiter plates and found that this lectin promotes th

69 lbicans strain SC5314 were formed in 96-well microtiter plates and on silicon elastomer pieces using

70 amenable to application in 96- and 384-well microtiter plates and should prove useful for high-throu

71 ng exposed acrylic groups, including plastic microtiter plates and silanized glass.

72 carbohydrates (6-16) were also displayed in microtiter plates and successfully screened with various

73 Immortalized human cells are grown in microtiter plates and treated with compounds from a smal

74 ns were used to directly coat the wells of a microtiter plate, and quantitation was achieved by using

75 nd titration, (v) dispensing of embryos into microtiter plates, and (vi) reporter quantification.

76 d FACS-sorted cells were added per well into microtiter plates, and after 11 days at 37 degrees C the

77 ction domains in individual wells of 96-well microtiter plates, and for quantifying domain-peptide in

78 Using pre-coated and blocked microtiter plates, and pre-prepared liposome reagents, a

79 pho-ERK, and the signals in the wells of the microtiter plate are quantified by a LI-COR infrared sca

80 els of cytochrome c contained in a 1536-well microtiter plate are shown.

81 print at > x 10 higher density on a standard microtiter plate area than currently possible, our cell

82 introduction into cells by transfection in a microtiter plate array.

83 use the substrate is covalently bound to the microtiter plate, artifacts such as pH-dependent displac

84 omain alone, increased initial attachment to microtiter plates, as did in trans expression of the A d

85 A microtiter plate assay based on the original quartz cuve

86 onstrate the accuracy and versatility of the microtiter plate assay by application to the kinetic ana

87 An automated electrochemical microtiter plate assay for the quantification of free ra

88 A microtiter plate assay format permitted a rapid determin

89 le and cost-effective nanoparticle method as microtiter plate assay format shows great potential for

90 tylation but does not inhibit trypsin, and a microtiter plate assay of the SIRTs has been devised usi

91 Hybridomas were selected using a microtiter plate assay that measured the pH-dependent de

92 ystems, this concept is applied to develop a microtiter plate assay to detect biotin (as a model for

93 throughput methyl viologen-based photometric microtiter plate assay was established to determine the

94 Biofilm formation was measured by using a microtiter plate assay with the crystal violet staining

95 We have developed and optimized a 96-well microtiter plate assay, based on the reduction of alamar

96 say systems, surface plasmon resonance and a microtiter plate assay, demonstrated that the beta3 A-do

97 es of avidin and horseradish peroxidase in a microtiter plate assay.

98 n of CTB produced by V. cholerae in a simple microtiter plate assay.

99 matographic column fractionation followed by microtiter plate assay.

100 ng abilities of the swarming mutants using a microtiter plate assay.

101 We then describe a direct fluorescent microtiter plate assay.

102 growth factors was assessed using a 96-well microtiter plate assay.

103 ropneumoniae serotype 5 itself, in a 96-well microtiter plate assay.

104 creened for biofilm-negative mutants using a microtiter plate assay.

105 antifungal activity were determined using a microtiter plate assay.

106 or biofilm formation by E. faecalis, we used microtiter plate assays and a chemostat-based biofilm fe

107 g beads accelerate amyloid fibrillization in microtiter plate assays are unclear.

108 levels were determined by standardized ELISA microtiter plate assays from a commercial (bFGF) or prop

109 Quantitative microtiter plate assays revealed marked differences in s

110 bes both thin-layer chromatography (TLC) and microtiter plate assays, which use bioluminescence or th

111 produces comparable results to conventional microtiter plate assays, yet requires 2 orders of magnit

112 s, NMR, isothermal titration calorimetry and microtiter plate assays.

113 405, and mixtures of the two organisms using microtiter plate assays.

114 to bovine submaxillary mucin in solid-phase microtiter plate assays.

115 d total assay time 2 fold in comparison with microtiter plate assays.

116 charide (LPS) content in solution in 96-well microtiter plates at room temperature.

117 antibodies and applied as a novel label in a microtiter plate based immunoassay and a quantitative co

118 Here we describe a fluorescently detected microtiter plate-based assay for inhibitor binding to HM

119 In the present study, we describe a microtiter plate-based assay for quantitation of the amo

120 acroglobulin capture to develop a sensitive, microtiter plate-based assay for serum chymase, assisted

121 using either a thin film biosensor chip or a microtiter plate-based assay.

122 A new format for the microtiter plate-based assays was proposed.

123 ing nitrocellulose-based CBM macroarrays and microtiter plate-based CBM capture and competitive-inhib

124 or maltose using amylose magnetic beads in a microtiter plate-based format.

125 ed and optimized methodology for the 96-well microtiter plate-based measurement of Histoplasma yeast

126 so demonstrated using this relatively simple microtiter plate-based polycation detection system.

127 Microtiter plate-based robotic electrochemical antioxida

128 tion and application of a spectrophotometric microtiter-plate-based assay for NAAAR.

129 Further two-hybrid analysis and microtiter plate binding assays localized the sites of i

130 mbiae BBMV and bound Cry11Ba on dot blot and microtiter plate binding assays with a calculated K d of

131 the MMAC1/ PTEN-PDZBD peptide inhibited both microtiter plate binding to the hDLG and hMAST205 PDZ do

132 Microtiter plate-binding assays, coprecipitation experim

133 Microtiter plate biofilm analyses indicated that biofilm

134 In microtiter plates, biotinylated high molecular weight ki

135 ge as the conventional method on the 96-well microtiter plate but has advantages such as less reagent

136 ing protein (PBP) constructs by compounds in microtiter plates by means of competition with time-depe

137 Binding assays performed in microtiter plates, by two-dimensional (2D) Western blott

138 A single 96-well microtiter plate can analyze approximately 20 specimens,

139 means for accessing samples serially from a microtiter plate, channels for assembling eight parallel

140 were screened by affinity selection using a microtiter plate coated with monoclonal antibodies.

141 lower quantities were sufficient to saturate microtiter plates coated with a limiting amount of anti-

142 re of the trkA receptor from cell lysates in microtiter plates coated with an anti-trk antibody.

143 ts were detected by hybridization to 96-well microtiter plates coated with either a HCMV- or an IS-sp

144 Incubation of purified sodium channels on microtiter plates coated with tenascin-C revealed satura

145 In ELISA, microtiter plates coated with zymosan induced efficient

146 s formed on peg lids can then be fitted into microtiter plates containing test agents.

147 For directed GOx evolution a microtiter plate detection system based on the quinone d

148 tive extraction were tested against standard microtiter plate ELISA.

149 In both a solution phase and a microtiter plate elongation assay, IAPP fibrils are poor

150 ed in a single well using a standard 96-well microtiter plate enzyme-linked immunosorbent assay (ELIS

151 ensitivity level reasonably close to that of microtiter-plate Europium nanoparticle assay.

152 ng 30 min of incubation and measurement in a microtiter plate fluorimeter.

153 d digestion and peptide elution into 96-well microtiter plates followed by LC-MS analysis.

154 cell culture virus isolation (VI) in 96-well microtiter plates, followed by immunostaining of cell mo

155 640 compounds in the footprint of a standard microtiter plate for the identification of novel agonist

156 d; thus, it can be directly carried out with microtiter plates for a large number of samples at room

157 say that can be conveniently performed using microtiter plates for the discovery and/or validation of

158 p10 manual pipette, or in a fully automated microtiter plate format (96 samples at a time) employing

159 The assay is carried out in a microtiter plate format and measures cellular proliferat

160 ion fluorescence activity assay to a 96-well microtiter plate format and uses a plate reader to detec

161 rescent assays for D-Ala were developed in a microtiter plate format based on d-aminoacid oxidase/hor

162 The assay performed in a 96-well microtiter plate format employs biotin-labeled gelatin (

163 The nanoparticles were used in a microtiter plate format for glycopeptide capture using a

164 report, a 14CO2-capture method in a 96-well microtiter plate format has been developed and a phospho

165 d has been adapted to a 384-well, low-volume microtiter plate format that can be used for the high-th

166 and the well-known ABTS-assay was applied in microtiter plate format to validate oxygen independency

167 onstrate the utility of this PETE assay in a microtiter plate format using the RNA-dependent RNA poly

168 gurations, we describe its use in a 96-well, microtiter plate format with a lower plate containing H2

169 tration determinations and was scaled to the microtiter plate format with appropriate mixing, dispens

170 hnologies for quantification of compounds in microtiter plate format without the need for authentic c

171 ower than 10%), and high throughput (96-well microtiter plate format) make this assay an excellent su

172 ODIPY-FL-casein assay is easily adapted to a microtiter plate format, so it can be used to screen lar

173 al model reactions which are compatible with microtiter plate format, such as monitoring enzymatic re

174 25I-labeled RIA ([125I] RIA) is adapted to a microtiter plate format, termed mini-RIA.

175 say was readily adapted for use in a 96-well microtiter plate format.

176 he reaction wells containing the probes in a microtiter plate format.

177 sponse curve for the analyte in a convenient microtiter plate format.

178 asure poly(A) polymerase (PAP) activity in a microtiter plate format.

179 rization of (33)P-rEBP and rEBP in a 96-well microtiter plate format.

180 ermination of PEG molecular weight (MW) in a microtiter plate format.

181 assay aspartyl-beta-hydroxylase activity in microtiter plate format.

182 the surface of individual pins arranged in a microtiter plate format.

183 ors in the presence of only 10 nM sirtuin in microtiter plate format.

184 as a ready-to-go assay was prepared for the microtiter plate format.

185 Rubidium flux was performed in a 96-well microtiter plate format; rubidium was quantified using a

186 d robust in nature, and also compatible with microtiter plate formats.

187 RBP4 in high-density 384-well and 1536-well microtiter plate formats.

188 e protocol is applicable to 96- and 384-well microtiter plate formats; uses a commercially available

189 These devices illuminate samples in microtiter plates from one side and use the RGB-based im

190 exin-V binding to phosphatidyl serine-coated microtiter plates, frozen thawed washed platelets, activ

191 The microtiter plate has been an essential tool for diagnost

192 ystem, the total analysis time for a 96-well microtiter plate has been reduced to approximately 5 min

193 nolates is widely used and a desulphation in microtiter plates has been applied to reach high through

194 rd assays typically are performed in 96-well microtiter plates having 200-microL well volumes and up

195 We have developed a novel 96-well microtiter plate high-throughput screening filtration as

196 We developed a 96-well microtiter-plate high-throughput screening (HTS) assay f

197 of 125I-labeled galectin-3 to IgE coated on microtiter plates; (ii) the galectin-3's hemagglutinatio

198 itopes markedly changed between the free and microtiter-plate immobilized state as revealed by antibo

199 ed as biolabels in quantitative fluorescence microtiter plate immunoassay and qualitative on-site col

200 We have developed a microtiter plate immunoassay for counting single molecul

201 l in wheat and maize samples by fluorescence microtiter plate immunoassay with an IC50 of 220 mug kg(

202 oped a sensitive Europium nanoparticle-based microtiter-plate immunoassay capable of detecting target

203 as several nanomoles can be determined in a microtiter plate in 10-20 min.

204 t, the same assay was performed in a 96-well microtiter plate in 200 microL using 30 min of incubatio

205 or a fluorescein attached to the wells of a microtiter plate in a competitive fashion.

206 erformed unattended runs of up to 17 96-well microtiter plates in 8h was constructed.

207 d the DropArray technology with conventional microtiter plates in a cell-based protein-binding assay.

208 e able to bind to fibronectin immobilized on microtiter plates in a concentration-dependent manner.

209 o collagens type I, II, and IV adsorbed onto microtiter plates in a dose-dependent saturable manner.

210 an also be printed into 96-well glass bottom microtiter plates in a multiplexed manner, and the fluor

211 time, show that genes that are close on the microtiter plates in microarray experiments also tend to

212 ion of mutant cells with cosmid DNA from two microtiter plates in the library produced colonies that

213 gmentation chain transfer) polymerization in microtiter plates in the open atmosphere.

214 d intracellular parasites were cultivated in microtiter plates in the presence of the color substrate

215 FP reporter cells were seeded into a 96-well microtiter plate, incubated for 24 h, and then treated w

216 e of a single-tube reaction in ligand-coated microtiter plates indicates the versatility of PRIME dis

217 Real time PCR (RT-PCR) in a microtiter plate is the preferred method for quantitativ

218 As it is based on a standard 96-well, microtiter plate, it is amenable to automation and high

219 assay is conveniently carried out in 96-well microtiter plates; it is ideally suited for assaying lar

220 ith the convenience and standardization of a microtiter plate, make arrays of SAMs a versatile tool t

221 epithelial cell lines by use of a sensitive microtiter plate method in which measurement of bacteria

222 tive enzyme-linked immunosorbent assay-based microtiter plate method is described for assaying this D

223 EK Diagnostic Systems, Cleveland, OH) uses a microtiter plate MIC format for susceptibility testing o

224 novel compounds at nominal levels of 10mM in microtiter plate (MTP) format.

225 Southern blotting, we evaluated colorimetric microtiter plate (MTP) systems from ViroMed Laboratories

226 A 96- or 24-well microtiter plate (MTP) was positioned on the gadget's sc

227 d covalently attached to a polystyrene based-microtiter plate (MTP), pretreated with KOH.

228 1:1 (v/v) and dispensed in a KOH-pretreated microtiter plate (MTP).

229 lane-functionalized 96-well chemiluminescent microtiter plates (MTP) using 1-ethyl-3-(3-dimethylamino

230 d and cost-effective cellphone-based 96-well microtiter-plate (MTP) reader, capable of performing AST

231 standard STREP-HRP colorimetric reaction in microtiter plates of differing optical quality produced

232 e enables combinatorial polymer synthesis in microtiter plates on the benchtop without the need of hi

233 assay (KIRA-ELISA), consists of two separate microtiter plates, one for cell culture, ligand stimulat

234 gnificant reductions in biofilm formation on microtiter plates or hydroxylapatite disks.

235 pecific capture probes were immobilized onto microtiter plates or silicon chips.

236 e small stationary volumes (e.g., wells of a microtiter plate) or flowing volumes of liquids (e.g., m

237 ridoma cells, as well as clonal expansion in microtiter plates over several weeks, and the number of

238 In addition to a qualitative colorimetric microtiter plate PCR assay (MTP-PCR) and a semiquantitat

239 Use of a 96-well microtiter plate permits automated and sensitive quantif

240 be similar to those generated using a manual microtiter plate procedure.

241 was attained for the on-cell assay using the microtiter plate reader approach, whereas as low as 2 mi

242 The device is then placed into a standard microtiter plate reader for measurement, with the entire

243 leased from mammalian cells using a standard microtiter plate reader to measure wells integrated into

244 e that the inner filter effect correction of microtiter plate reader velocities enables rapid measure

245 ntracellular C1-BODIPY-C12 fluorescence on a microtiter plate reader, whereas extracellular fluoresce

246 croscope and quantification after lysis in a microtiter plate reader.

247 ligation and detection using a fluorescence microtiter plate reader.

248 bda(ex)=379 nm and lambda(em)=513 nm using a microtiter plate reader.

249 sity of which can then be determined using a microtiter-plate reader.

250 ws measurements of the reactions by standard microtiter plate readers without any additional steps in

251 ity is incompatible with enhanced throughput microtiter plate screening.

252 ed to the bioactive surface of scintillating microtiter plates served as the basis to evaluate enzyme

253 ows them to be arrayed in a standard 96-well microtiter plate spacing, making this device ideal for h

254 the results obtained with a PCR colorimetric microtiter plate system by use of clinical CSF specimens

255 the integration of these arrays with 96-well microtiter plate technology to create microarrays in mic

256 uent into a system that can be combined with microtiter plate technology.

257 r to subsequent merging of microfluidics and microtiter-plate technology for high-throughput assessme

258 detection of a sandwich hybridization, in a microtiter plate, that occurs in a single step.

259 tests can be performed simultaneously in one microtiter plate, the assay is ideal for evaluation of a

260 ls were placed in the stroma-coated wells of microtiter plates, the percentage of wells with leukemic

261 phase approach, SPEG can be performed with a microtiter plate to provide a high-throughput platform f

262 adily multiplexed and scaled up in multiwell microtiter plates to allow simultaneous parallel detecti

263 ed antiglobulin bound to streptavidin-coated microtiter plates to immobilize antiphospholipase C-gamm

264 s only 100 ng of input RNA and uses standard microtiter plates to process samples in parallel.

265 The AK assay is performed in a single microtiter plate using an 'add and read' procedure that

266 ed 450 high-confidence interactions using 47 microtiter plates, versus thousands of plates expected u

267 d into six 96-well (576 total) polypropylene microtiter plates via a fraction collector.

268 and most related analogs to the wells of the microtiter plate was found to occur in the first 5 min o

269 The microtiter plate was placed vertically on a three-dimens

270 of acapsular S. aureus to fibrinogen-coated microtiter plates was enhanced.

271 screens, and mutant recovery all in 96-well microtiter plates, we have scaled up this approach to is

272 ured by one set of antibodies immobilized in microtiter plate wells and detected using a second antib

273 The assay is carried out in microtiter plate wells and therefore offers the potentia

274 When HDMVEC were cultured in microtiter plate wells coated with concentrations of C1q

275 immunoassay was performed in antigen-coated microtiter plate wells for simultaneous qualitative and

276 Microtiter plate wells modified with thin (approximately

277 Capture DNA is conjugated to the surface of microtiter plate wells through a biotin-streptavidin int

278 es can be predried to the assay vials, e.g., microtiter plate wells, and readout is ready in 10 min a

279 proteins, but not fibronectin-coated plastic microtiter plate wells, was specifically blocked by anti

280 fibronectin, collagen IV, and laminin-coated microtiter plate wells, with the rank order of attachmen

281 ransfer to a polymeric substrate coated onto microtiter plate wells.

282 and the amount of substrate used to coat the microtiter plate wells.

283 amperometric sensing of glucose solutions in microtiter-plate wells used computer-controlled stepper

284 wn by enzyme-linked immunosorbent assay when microtiter plates were coated with platelet membrane pro

285 ts of custom-made frozen 96-well polystyrene microtiter plates were used and prepared with 2x predilu

286 The HNO-sensing microtiter plates were used to quantify pH-dependent HNO

287 The assay was adapted to microtiter plates, which permits a large number of sampl

288 of a PIC integration assay using DNA-coated microtiter plates, which speeds assays of PIC integratio

289 us to monitor protein unfolding in a 96-well microtiter plate with a UV plate reader.

290 P can quantify an analyte as precisely as in microtiter plate with insignificant non-specific binding

291 by functionalizing a KOH-treated polystyrene microtiter plate with multiwalled carbon nanotubes (MWCN

292 Here, we show that simultaneous treatment of microtiter plates with chitosan, a deacetylated form of

293 yme A reductase (HMGR) inhibitors in 96-well microtiter plates with rapid workup using established ma

294 By co-coating microtiter plates with SNAP25 substrate and a monoclonal

295 Precoating of microtiter plates with two species of oxidized A2E, pero

296 mpounds against aminopeptidase M in 384-well microtiter plates with Z factors ranging from 0.53 to 0.

297 e introduction from a commercially available microtiter plate without the need for a separate fluid d

298 f 96-well or 384-well density PPSF-resistant microtiter plates without the requirement for multiple o

299 se assay is done in a single tube (well of a microtiter plate), without separation, precipitation, or

300 Our platform is an ideal alternative to the microtiter plate, works with different volumes, is compa