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

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

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

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

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

9 an enzyme amplification cascade in the same microtiter plate.

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

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

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

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

14 thod that employs I-PhiAB6TSP immobilized on microtiter plate.

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

16 Milk also removes ricin bound to the microtiter plate.

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

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

19 t efficiently reduces nonspecific binding on microtiter plates.

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

21 ntifying CTB bound on epithelial surfaces in microtiter plates.

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

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

24 -triphosphate (ATP) bioluminescence assay in microtiter plates.

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

26 enables nESI-MS based HTS assays in 96-well microtiter plates.

27 of in vitro biofilm formation on polystyrene microtiter plates.

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

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

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

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

32 ploying native enzyme that is immobilized on microtiter plates.

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

34 to high molecular weight kininogen linked to microtiter plates.

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

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

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

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

39 The library is arrayed in microtiter plates.

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

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

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

43 ays running at low sirtuin concentrations in microtiter plates.

44 compared with static protocols performed in 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 proximately 17 pCi/ well (or 1.6 nCi/96-well microtiter plate) 14C-1A5 was used, which is far below t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

81 A microtiter plate assay based on the original quartz cuve

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

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

84 A microtiter plate assay format permitted a rapid determin

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

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

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

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

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

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

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

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

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

94 antifungal activity were determined using a microtiter plate assay.

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

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

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

98 We then describe a direct fluorescent microtiter plate assay.

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

100 matographic column fractionation followed by microtiter plate assay.

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

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

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

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

105 Quantitative microtiter plate assays revealed marked differences in s

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

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

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

109 405, and mixtures of the two organisms using microtiter plate assays.

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

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

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

113 developed to handle 12 samples (one row of a microtiter plate) at a time.

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

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

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

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

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

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

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

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

122 COS available, we have developed a two-step, microtiter plate-based high-throughput screening assay t

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

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

125 Microtiter plate-based robotic electrochemical antioxida

126 me investment for conventional agar plate or microtiter plate-based screening assays represents a maj

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

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

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

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

131 Microtiter plate-binding assays, coprecipitation experim

132 Microtiter plate biofilm analyses indicated that biofilm

133 In microtiter plates, biotinylated high molecular weight ki

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

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

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

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

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

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

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

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

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

143 In ELISA, microtiter plates coated with zymosan induced efficient

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

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

146 tive extraction were tested against standard microtiter plate ELISA.

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

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

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

150 r nanoparticle assay (MINA) are assembled in microtiter plates fitted with magnetic inserts.

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

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

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

154 640 compounds in the footprint of a standard microtiter plate for the identification of novel agonist

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 tibility of the immunoassay with the 96-well microtiter plate format, a stop reagent, containing form

172 ing aptamers against protein biomarkers in a microtiter plate format, obliterating the need for multi

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

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

175 25I-labeled RIA ([125I] RIA) is adapted to a microtiter plate format, termed mini-RIA.

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

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

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

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

180 rization of (33)P-rEBP and rEBP in a 96-well 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 ermination of PEG molecular weight (MW) in a microtiter plate format.

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

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

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

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

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

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

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

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

192 The microtiter plate has been an essential tool for diagnost

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

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

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

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

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

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 In a microtiter plate immunoassay, individual sandwich immune

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

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

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

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

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

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

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

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

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

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

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

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

215 of individual nanoliter-scale droplets from microtiter plates, including the first demonstration of

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

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

218 s to deliver analyte molecules directly from microtiter plates into the mass spectrometer at subsecon

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

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

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

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

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

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

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

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

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

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

229 1:1 (v/v) and dispensed in a KOH-pretreated microtiter plate (MTP).

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

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

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

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

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 ntional ELISA-based sandwich immunoassays on microtiter plates, our microfluidic setup offers a 25-50

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

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

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

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

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

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

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

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

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

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

248 ligation and detection using a fluorescence microtiter plate reader.

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

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

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

252 A panning in microtiter plates resulted in 22 unique in vitro neutral

253 ity is incompatible with enhanced throughput microtiter plate screening.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 ies in a circular pattern at the bottom of a microtiter plate well.

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

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

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

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

278 ple droplets are acoustically dispensed from microtiter plate wells into a continuous fluid transfer

279 Microtiter plate wells modified with thin (approximately

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

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

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

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

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

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

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

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

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

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

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

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

292 cessing is performed in standardized 96-well microtiter plates with commonly available laboratory ins

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