ライフサイエンスコーパス: microtiter

1 ved for Fg in all FnBPA variants tested with microtiter.

2 Microtiter 96-well and three-dimensional cell-based micr

3 Here we used microtiter and atomic force microscopy (AFM) to investig

4 n biofilm initiation, as confirmed by static microtiter and continuous culture flow cell and tubing b

5 The microtiter array including IID sensors 1 and 2 is capabl

6 Here, the characterization of sensors and microtiter arrays comprising the IIDA are reported.

7 A microtiter assay was developed for the improved detectio

8 AMP reaction, and a quantitative cohemolysis microtiter assay was developed using purified sphingomye

9 , the level of biofilm formation in a static microtiter assay was diminished in T2S mutants.

10 Using a plasma-coated microtiter assay, biofilm formation was restored to the

11 For the microtiter assay, either spent bacterial culture superna

12 d in a modified version of the 96-well plate microtiter assay.

13 We employed this microtiter-based assay to determine the antifungal susce

14 wo Petri dishes connected with tubing; and a microtiter-based assay.

15 sing SPR is feasible and has advantages over microtiter-based binding assays, especially under flow c

16 om different epithelial sites, using SPR and microtiter-based binding assays.

17 A simple, rapid, and reproducible microtiter-based chondroitinase (CSase) assay is reporte

18 ribe a rapid and highly reproducible 96-well microtiter-based method for the formation of fungal biof

19 In contrast with microtiter-based screening, this system does not involve

20 lectrodes integrated within ultra-low-volume microtiter chambers for the amperometric determination o

21 s is a versatile method that can be used for microtiter determinations of biofilm antimicrobial susce

22 tibility to chlorhexidine gluconate (CHG) by microtiter dilution; mupirocin susceptibility was tested

23 The microtiter dish assay is a more expedient method for mea

24 We report here the development of a 96-well microtiter dish assay.

25 oughput sample analysis of APR activity in a microtiter dish format.

26 iene C(4) (LTC(4)) was measured in a 96-well microtiter dish with rapid filtration onto a Perkin Elme

27 In an earlier report, we optimized a microtiter format assay system to screen potential bioac

28 Additionally, in the microtiter format, multiple sets of kinetic experiments

29 We adapted the FD sensors to microtiter format, where they allow high-throughput scre

30 amster ovary cells, in both microfluidic and microtiter formats.

31 by subsequent optimization through iterative microtiter library synthesis followed by in situ activit

32 Testing was performed in frozen microtiter panels according to the Clinical and Laborato

33 lts were compared to those of a colorimetric microtiter PCR enzyme immunoassay (PCR-EIA) used as a di

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

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

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

37 1:1 (v/v) and dispensed in a KOH-pretreated microtiter plate (MTP).

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

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

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

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

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

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

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

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

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

47 A microtiter plate assay based on the original quartz cuve

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

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

50 A microtiter plate assay format permitted a rapid determin

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

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

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

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

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

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

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

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

59 antifungal activity were determined using a microtiter plate assay.

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

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

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

63 matographic column fractionation followed by microtiter plate assay.

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

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

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

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

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

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

70 405, and mixtures of the two organisms using microtiter plate assays.

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

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

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

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

75 Microtiter plate biofilm analyses indicated that biofilm

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

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

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

79 tive extraction were tested against standard microtiter plate ELISA.

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

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

82 640 compounds in the footprint of a standard microtiter plate for the identification of novel agonist

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 25I-labeled RIA ([125I] RIA) is adapted to a microtiter plate format, termed mini-RIA.

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

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

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

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

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

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

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

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

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

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

108 The microtiter plate has been an essential tool for diagnost

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

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

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

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

113 In a microtiter plate immunoassay, individual sandwich immune

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

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

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

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

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

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

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

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

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

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

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

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

126 ligation and detection using a fluorescence microtiter plate reader.

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

128 ity is incompatible with enhanced throughput microtiter plate screening.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

162 Microtiter plate-based robotic electrochemical antioxida

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

164 Microtiter plate-binding assays, coprecipitation experim

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

166 Milk also removes ricin bound to the microtiter plate.

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

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

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

170 erformed simultaneously in single wells of a microtiter plate.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

199 In ELISA, microtiter plates coated with zymosan induced efficient

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

236 In microtiter plates, biotinylated high molecular weight ki

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

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

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

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

241 t efficiently reduces nonspecific binding on microtiter plates.

242 of an appropriate desulphation procedure in microtiter plates.

243 ommended for high throughput desulphation in microtiter plates.

244 ubculturing visibly clear wells from the MIC microtiter plates.

245 aphic resins aliquotted in membrane-bottomed microtiter plates.

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

247 ntifying CTB bound on epithelial surfaces in microtiter plates.

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

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

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

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

252 of in vitro biofilm formation on polystyrene microtiter plates.

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

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

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

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

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

258 ploying native enzyme that is immobilized on microtiter plates.

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

260 to high molecular weight kininogen linked to microtiter plates.

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

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

263 ays running at low sirtuin concentrations in microtiter plates.

264 compared with static protocols performed in microtiter plates.

265 borosilicate glass surfaces and polystyrene microtiter plates.

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

267 Microtiter proliferation assays revealed that the Tax-1

268 sub-second positioning of any location on a microtiter-sized target with up to 1536 samples with mic

269 tibodies to respective nitro-explosives on a microtiter strip, resulting in the formation of specific

270 ility of this glycosaminoglycan to adhere to microtiter surfaces.

271 I guidelines using a custom, broth dilution, microtiter system.

272 ence of treated versus untreated polystyrene microtiter trays on caspofungin MICs using 209 isolates

273 sites found nonspecifically in conventional microtiter well assays.

274 describe simple screens using red cells in a microtiter well format to identify intercalating agents

275 mmobilize the enzyme on a solid surface in a microtiter well format.

276 occus aureus biofilms was investigated using Microtiter Well Plates (MWP) and Drip Flow Reactors (DFR

277 Chitin-coated microtiter well plates captured a CBD-tagged heterodimer

278 e, similar in size and pitch to conventional microtiter well plates, but offer electrodes along the i

279 sable pipet tips and conventional disposable microtiter well plates.

280 carbon chain that noncovalently binds to the microtiter well surface.

281 and 200 eukaryotic cells were measured in a microtiter well under the optimized conditions.

282 t hearts; cells were plated (5 x 10(4) cells/microtiter well) and challenged with either vehicle or n

283 PSA antibody immobilized to the surface of a microtiter well, (2) PSA, and (3) an anti-PSA antibody-U

284 ome this problem, we designed an alternative microtiter well-based binding assay in which Gluc is cap

285 in individual aquatic invertebrates kept in microtiter well-plates.

286 poB) was measured by capturing h-apoB-100 in microtiter wells and detecting OxPL by antibody E06.

287 and were defective in pellicle formation in microtiter wells and in a biofilm attachment assay.

288 )beta(3) bound in a dose-dependent manner to microtiter wells coated with the isolated 190-kDa proteo

289 eterize the unique features occurring within microtiter wells containing specific growth media source

290 In microtiter wells factor XI binds to more sites in the ab

291 ssive noncovalent adsorption of heparin onto microtiter wells following their treatment by plasma pol

292 enterica grown either in polyvinyl chloride microtiter wells or in urethral catheters.

293 eating the specific immuno-complex formed on microtiter wells resulted in thermal lysis of nitro-expl

294 Isolates formed biofilms in microtiter wells to various degrees.

295 ormat onto the bottom of streptavidin-coated microtiter wells.

296 VCAM-1 and 7d-VCAM-1 coated onto polystyrene microtiter wells.

297 tachment of the tested strain to polystyrene microtiter wells.

298 (B)) necessary for coupling to avidin coated microtiter wells.

299 ormat onto the bottom of streptavidin-coated microtiter wells.

300 nd reduced GBS binding to fibronectin-coated microtiter wells.