ライフサイエンスコーパス: plating

1 urrent of mid-stage hES-CMs (20-35 days post plating).

2 ta-glycerol phosphate to cells at 64 h after plating.

3 ng, in some cases nearly 2 years postinitial plating.

4 nced activation of ERK following fibronectin plating.

5 ed ERK activation in response to fibronectin plating.

6 s may be best treated with locked nailing or plating.

7 me, being wider on day 1 than on day 2 after plating.

8 as determined with calcein-AM 24 hours after plating.

9 followed by overnight enrichment in TSB and plating.

10 ving intramedullary nailing in comparison to plating.

11 y-forming units were then counted 40 h after plating.

12 rmation of cobblestone colonies on secondary plating.

13 es C is at least as good as that from direct plating.

14 kjet printing and subsequent chemical copper plating.

15 ional silver mirror reaction and electroless plating.

16 gnificantly higher carriage rate with direct plating (11.8 versus 6.1%; P < 0.001).

17 transport medium at room temperature before plating, 51% used Campy blood agar plate medium, 52% rea

18 ere positive for pneumococci from the direct plating; 94 (98%) of these were positive from the fresh

19 e of cross-contamination was demonstrated by plating a total of 200 alternating inoculated and steril

20 tic conditions in the presence of particular plating additives (SPS, Imep, PEI, and PAG) used in the

21 To probe the trend of these plating additives toward inclusion into the deposit upon

22 nificantly more VRE isolates than did direct plating alone (28 versus 18 VRE isolates, respectively).

23 PPy-chitosan plating also improved electric coupling between skeletal

24 at low temperature metal pastes, electroless plating and atomic layer deposition can all be used with

25 atients by selective and nonselective direct plating and broth enrichment.

26 limitations, including labor-intensive agar plating and colony selection methods associated with the

27 resenting four different periods: (i) manual plating and conventional biochemical identification (CON

28 g development, with levels peaking 7 d after plating and declining thereafter.

29 greement was 83.5% The time interval between plating and final organism identification was decreased

30 of detection of E. coli O157 by both direct plating and IMS was highly dependent upon the initial co

31 concentrations is very poor for both direct plating and IMS.

32 n sensory neurons and L7 begins by 3 h after plating and is accompanied by a rapid accumulation of a

33 s were developed and implemented to minimize plating and liquid handling errors, reduce dead times wi

34 ochemical identification (CONV), (ii) manual plating and MALDI-TOF MS identification (MALDI), (iii) M

35 hout the tissue extraction, serial dilution, plating and manual scoring involved in standard assays o

36 creased available surface for homogeneous Li plating and minimize volume fluctuation of Li electrodes

37 cells with two mutations, one formed before plating and one after.

38 OM crystal adhesion reached a peak 2 d after plating and progressively fell thereafter.

39 technique to impose the exhaustive oxidative plating and re-reduction of halides on the silver elemen

40 Both the plating and replication efficiencies of ICP0- viruses we

41 Results were further validated by plating and sequencing of individual colonies, and also

42 anodes suffer from poor reversibility during plating and stripping processes due to their high reacti

43 overcome is the inferior reversibility of Li plating and stripping, typically thought to be related t

44 However, under repeated plating and stripping, zinc metal anodes undergo a well-

45 and the other transported in BHI followed by plating and subculturing in an enrichment medium, provid

46 nstrate the effects of two strategies, pulse plating and the use of electrolyte additives.

47 s 2.11 times higher in patients who received plating and this reached statistical significance (95% C

48 plating with the same instrument (replicate plating) and of the consensus agreement between the two

49 face activity, retarded cell spreading after plating, and led to the formation of immobile, tightly a

50 oast by plating on mCPC agar, enrichment and plating, and quantitative PCR (qPCR).

51 By using cell fractioning, plating, and single-cell fluorescent microscopy, we find

52 , coating the template by electroless nickel plating, and subsequently etching away the template.

53 aluated cross-contamination, the accuracy of plating, and the quality of the results.

54 nrichment in salt-containing TSB followed by plating; and Stuart's preincubation for 72 h followed by

55 brid In-Li anodes that use both alloying and plating approaches for charge storage.

56 It also enhances efficient hPSC plating as single cells.

57 new gene activities, a simple and versatile plating assay was developed in Saccharomyces cerevisiae

58 Bacterial viability was assessed by plating assay, and TNF-alpha release was measured by enz

59 Re-plating assays of primary RB1(-/-) calvarial cells after

60 olony-forming cells, by performing secondary plating assays.

61 Clonogenic (single-cell plating) assays were used to define and quantify subpopu

62 | Li cell during repeated lithium stripping/plating at room temperature, with a current density of 0

63 an appropriate medium (NS-A+B27 supplement), plating at sufficient densities (>5 cells per mm(2)), an

64 ersus Li(+)/Li, avoiding problematic lithium plating at the expense of reduced cell voltage.

65 ransiently, peaking within a few hours after plating, at which time the protein was in the form of pe

66 position can significantly alter the lithium plating behavior, affording a promising route to suppres

67 including surface functionalization and cell plating, can be completed in 10 h.

68 d by incubating cultures with gentamicin and plating cell lysate on agar.

69 as TGF-beta2 production was not inhibited by plating cells on a synthetic nanofiber matrix with a thr

70 subcellular regions of cells is achieved by plating cells on an electrode array created by standard

71 In contrast, plating cells on collagen I triggered a TGFbetaRI kinase

72 After plating cells on fibrinogen, complexes of alphaIIbbeta3-

73 CLANs were induced by plating cells on fibronectin (a beta1 integrin ligand) i

74 We now report that plating cells on fibronectin triggers association of Grb

75 to take approximately 3 d (from the time of plating cells on imaging dishes).

76 h recording method was used to determine how plating cells on laminin (20 microg ml(-1); >2 h) alters

77 By plating cells on media that do not support plasmid repli

78 This includes plating cells on six-well tissue culture plates or imagi

79 At 21 days post-plating, co-cultures were deformed to 0.50 shear strain

80 on potential of the fusion protein in serial plating colony assays.

81 Here we show a backside-plating configuration that enables long-term cycling of

82 a-Bertani (LB) medium, as well as a profound plating defect.

83 ntal conditions such as cell cycle phase and plating delay (correlation between modelled and observed

84 a stable density of approximately 40% of the plating density for more than 30 days.

85 is integrated model to examine the effect of plating density on tissue growth via autocrine/paracrine

86 ly exposing to serum at a contact-inhibiting plating density, TKT loss was inhibited.

87 junction communication level and fibronectin plating density.

88 this localization pattern is insensitive to plating density.

89 ntified a critical boundary 16 to 20 h after plating during which bFGF induced MAPK activity is able

90 14 days of progressive activation following plating, during which time alpha-smooth muscle actin (al

91 s in ESwab tubes, the manual method and WASP plating each yielded 90 potential pathogens.

92 The plating efficiencies and shelf lives of locally made buf

93 or expression correlated with alterations in plating efficiencies but with modest affects on growth.

94 Double dnaA seqA mutants exhibited plating efficiencies much superior to wild-type strains

95 Utilizing a difference in plating efficiencies, we were able to enrich the neuron

96 ly burst-forming unit-megakaryocytes, with a plating efficiency >60% at the single-cell level.

97 mined to investigate nonheritable changes in plating efficiency and burst size that depended on which

98 transgenic keratinocytes show alterations in plating efficiency and calcium-induced differentiation,

99 and NPC cells inhibited cell proliferation, plating efficiency and migration, and enhanced sensitivi

100 further investigated using a more-sensitive plating efficiency assay.

101 nstrate differences in cellular viability or plating efficiency but did exhibit a decreased replicati

102 We have found, however, that the enhanced plating efficiency did not occur when cells were synchro

103 Their HSC have an increased plating efficiency in vitro, engraft at least as well as

104 Peak plating efficiency occurred as cells cycled out of G1 an

105 cetylated low-density lipoprotein) colonies (plating efficiency of 3%).

106 This lab reported previously that the plating efficiency of a herpes simplex virus type 1 ICP0

107 ine deprivation alone is able to enhance the plating efficiency of an ICP0(-) virus and that isoleuci

108 To quantitate the plating efficiency of CD34(+) cells that give rise to en

109 s, as well as the cloning vector, reduce the plating efficiency of HeLa cells.

110 We now report that the plating efficiency of ICP0- viruses is not enhanced at a

111 on the isogenic F(-) strain or as a reduced plating efficiency of the F(+) strain on solid media; at

112 d in five of eight plaques of T2294, and its plating efficiency under foscarnet was increased approxi

113 d into S phase, suggesting that the enhanced plating efficiency was due to cellular activities presen

114 PALB2-deficient cells, a severe reduction in plating efficiency was observed, with many abortive atte

115 (+) strain on solid media; at 2% bile salts, plating efficiency was reduced 10(4)-fold.

116 east one year, with the post-thaw viability, plating efficiency, and full retention of pluripotent ph

117 Dicumarol also inhibited cell growth, plating efficiency, and growth in soft agar.

118 exhibited an elongated cell cycle, decreased plating efficiency, and reduced DNA synthesis compared w

119 (ES) cells lacking Cfp1 exhibit a decreased plating efficiency, decreased cytosine methylation, elev

120 These cells showed decreased plating efficiency, elongated cell population doubling t

121 yers prior to infection resulted in enhanced plating efficiency.

122 tions, mutations, micronuclei, and decreased plating efficiency.

123 rs is the primary determinant of ICP0- virus plating efficiency.

124 mu could not be attributed to variations in plating efficiency.

125 ssing cells were indicated by: (a) decreased plating efficiency; (b) elongated cell population doubli

126 a simple magnetic separation without a large plating effort.

127 However, a Nafion((R)) coated copper plating electrode shows a successful decrement of the in

128 ous starch compared to the spray dried HOSO, plating flavour oils on porous starch could be a suitabl

129 n donors were analyzed within 48 hours after plating for E-cadherin gene and protein expression (by R

130 wing cells to atmospheric levels of O(2) and plating for survivors at 2-h time intervals.

131 mycin broth enrichment is superior to direct plating for the detection of vancomycin-resistant entero

132 dvantage over conventional direct blood agar plating for the diagnostic confirmation of bartonellosis

133 disaggregating the clumps, then diluting and plating for viable cell enumeration.

134 es by a conventional method that used direct plating from the transport/storage medium (50 specimens

135 ns that were negative by conventional direct plating from transport medium (range of numbers of posit

136 Here, we demonstrate that plating GI-101A human breast cancer cells on hard (0.9%)

137 Patients who received plating had a 2.19 times increased risk of treatment fai

138 ntramedullary nailing and submuscular bridge plating have also recently been reported to produce exce

139 Dissecting the hippocampus and plating hippocampal neurons takes 2-3 h.

140 ynapsin III was suppressed immediately after plating, hippocampal neurons extended minor processes bu

141 Bacterial colonization was determined by plating homogenates onto MacConkey agar, and immunofluor

142 noelectrodes are prepared by electrochemical plating in a laser-pulled quartz nanopipette tip immerse

143 of NT-3 is detectable in cultured SGNs after plating in either depolarizing or nondepolarizing medium

144 ion capacity compared to wt controls upon re-plating in methylcellulose supplemented with interleukin

145 Single cell plating in serum-free medium allows direct assessment of

146 Twenty-four hours after plating in serum-free medium, cultures were exposed to D

147 de direct plating onto solid medium or later plating in the laboratory.

148 he broth enrichments were superior to direct plating in their ability to detect E. coli O157:H7.

149 fferentiated hepatocytes through day 30 post plating, including liver-specific gene expression.

150 st evaluation of a new microbiology specimen-plating instrument, the WASP, which offers opportunities

151 We observed that derivation from plating intact human blastocysts resulted predominantly

152 Intramedullary fixation rather than plating is preferred, and allowing early protected weigh

153 scopic fluorescent plaque in a Petri dish by plating it in a host bacterial medium.

154 This motility defect is rescued by plating knockdown cells on preformed laminin-332 matrix.

155 ed a modified culture protocol that included plating larger volumes of urine, incubation under varied

156 s are defined as bacterial CFU enumerated by plating lung homogenates; total counts are defined as ba

157 Two to 4 days after plating, many cells underwent spontaneous contraction an

158 lent long-term functional outcomes; however, plating may lead to a higher risk of treatment failure a

159 rmined from unstimulated saliva on CHROMagar plating medium.

160 Such a backside-plating method can be applied to not only zinc metal sys

161 urthermore, we show here that an electroless plating method can be used to deposit a gold nanotube wi

162 g of the nerve fibers; (2) an adaptable drop-plating method for selective cell attachment, removal of

163 induced chondrogenesis, using a novel direct plating method in which intervening embryoid body format

164 (4.5 microm) is achieved via an electroless plating method involving initial reaction of the particl

165 An electroless gold plating method was used to deposit Au nanotubules within

166 Compared to the conventional agar plating method, the assay was rapid (1.5 h) and showed h

167 these observations using standard bacterial plating methods.

168 st probable numbers" method and conventional plating methods.

169 Among the four media evaluated with direct plating, MSAL(Ox) was 11 to 25% more sensitive for detec

170 Approximately 1 month after plating, multiple clusters of very small cells became ap

171 Lastly, for the plating of 113 specimens in ESwab tubes, the manual meth

172 erase beta' subunit and is nonpermissive for plating of bacteriophage P2.

173 dly phosphorylated on tyrosine residues upon plating of bone marrow-derived DCs (BMDCs) on integrin a

174 GDPD activity, adsorption, and efficiency of plating of Ca(2+) ions supports a role for GDPDLd17 acti

175 We previously reported that short-term (2 h) plating of cat atrial myocytes on the extracellular matr

176 In the present study direct plating of cattle feces was compared to three different

177 ny color with stock cultures and with direct plating of clinical specimens.

178 rical coding and identification (through the plating of different metal markers and of multimetal red

179 Encoded redox rods, prepared by sequential plating of different metal tracers into the pores of a h

180 Starting with the plating of digested tissue material, full-grown organoid

181 Direct plating of dilutions of bovine feces on SMACct can be us

182 mmunomagnetic separation (IMS) and to direct plating of dilutions of bovine feces onto sorbitol MacCo

183 The pores are fabricated by electroless plating of gold into the nanopores of an NCAM (Au-NCAM).

184 ed electrochemical synthetic route involving plating of indium into the pores of a host membrane.

185 The plating of lithium metal within the interior of the poro

186 isruption of the actin cytoskeleton, whereas plating of melanoblasts on an ephrin-B substratum induce

187 Here we report the defect-induced plating of metallic lithium within the interior of a por

188 which offers opportunities for the automated plating of microbiology specimens to an extent that has

189 Compared to PCR, direct plating of nasal swabs performed poorly, especially for

190 Subsequent isolation and plating of nonadherent FL-derived VEGFR-2(+) cells with

191 bla(KPC) from enrichment broth versus direct plating of rectal surveillance swabs on two selective cu

192 Direct plating of rectal swabs onto MacConkey agar containing 1

193 Therefore, direct plating of rectal swabs onto selective medium proved to

194 e completed in approximately 8 h and include plating of serum-deprived VSM or ASM cell suspension on

195 the effects are unique to perlecan, because plating of SMCs on several other basement membrane prote

196 , with this association being abrogated upon plating of the cells onto vitronectin.

197 r operates by the exhaustive electrochemical plating of the halides from the thin layer sample onto a

198 ]) in restrictive cells, we noticed that the plating of the ICP22 null (d22) and 3xstop mutants was r

199 Plating of these cells resulted in the formation of adhe

200 Plating of urine specimens with the WASP was compared to

201 abbit corneal epithelial cells is reduced by plating on a basement membrane-like extracellular matrix

202 ved growth factor (PDGF) and prepolarized by plating on a fibronectin line substrate exhibit persiste

203 , polymyxin, bacitracin, and lactose) and by plating on antibiotic-containing media (MacConkey agar w

204 A culture method utilizing quantitative plating on antibiotic-containing media has been proposed

205 Upon plating on basement membrane Matrigel, NIH3T3 cells form

206 differential broth and compared it to direct plating on bile esculin azide (BEA) agar for the isolati

207 chment is not required for apoptosis because plating on bovine serum albumin-blocked poly-L-lysine (a

208 Plating on control surfaces with TGFbeta induced hypermo

209 An increase in apoE synthesis after plating on fibronectin could be observed by 2 h and was

210 gher percentage of spreading cells 1 h after plating on fibronectin-coated plates than keratinocytes

211 ons in the isolates were readily obtained by plating on gemifloxacin- or moxifloxacin-containing agar

212 of cortactin-KD cells were fully rescued by plating on increasing concentrations of exogenous ECM.

213 Plating on LN5' triggered smad nuclear translocation, an

214 which a 10-mug meropenem disk was placed and plating on MacConkey agar after overnight enrichment of

215 ter and oysters from Florida's Gulf Coast by plating on mCPC agar, enrichment and plating, and quanti

216 more convenient than traditional spontaneous plating on metallic discs, and similar yields were obtai

217 ated rayon), which were processed by primary plating on MSA, MSA(Ox), MHA(Ox), and MSAL(Ox); Stuart's

218 irect transformation of growing cultures and plating on selective media.

219 Among positive samples identified by direct plating on SMACct, the direct counts of E. coli O157:H7

220 more rapidly than wild-type cells following plating on surfaces that cross-linked cellular beta2 int

221 igated by using three different methods: (i) plating on Thayer-Martin selective medium and testing by

222 V versus Li(+)/Li and can result in lithium plating on the graphite surface, raising safety concerns

223 Stuart's preincubation for 72 h followed by plating on the solid media; overnight enrichment in salt

224 motes actin-stress fiber formation following plating onto an integrin activating substrate whereas Fl

225 broth with 6.5% sodium chloride) followed by plating onto CHROMagar MRSA medium (broth-enriched CM cu

226 nt manner compared to the levels observed on plating onto fibronectin in the absence of stimulation.

227 Routine methods include direct plating onto solid medium or later plating in the labora

228 ssay, compared to detection by either direct plating or enrichment broth selective culture methods.

229 emoval of substrate interface by shadow mask-plating, or inhibition of Rho kinase or nonmuscle myosin

230 , human factors (lack of strict adherence to plating order, leading to only intermittent observation

231 The dissection and plating out of neurons takes 3-4 h and neurons can be ma

232 dishes and a further 3-4 h for isolation and plating out the cells.

233 her than that on SF at 24 and 72 hours after plating (P = 0.001 and 0.0005, respectively).

234 Axons grew up to 200 microm within 1 day of plating P19 embryoid bodies on laminin-1 (EHS laminin).

235 After infecting and plating phage on a hfl- bacterial host, cII mutants were

236 asurement parameters, 0.1 M HCl electrolyte, plating potential of 0 mV, and staircase scan mode were

237 atteries (SIBs) (0.01 V), and well above the plating potential of metal.

238 Plating primary human keratinocytes on the gamma2 precur

239 s excellent guides in which the Li stripping/plating process can take place and effectively confine t

240 finite volume change during the Li stripping/plating process results in cracks and fractures of the s

241 Given the stochasticity of the plating process, we show that the number of atoms plated

242 plating solution, indicating a reproducible plating processes.

243 (90 mV at 3 mAcm(-2)), more-stable stripping/plating profiles, and better cycling performance ( appro

244 ults suggest that intramedullary nailing and plating provide equivalent long-term functional outcomes

245 %, and 97% of samples respectively by direct plating, qPCR, and enrichment.

246 control of the arrival of ions and thus the plating rate on the Bi UME, to one ion every few seconds

247 The replicate plating results were comparable for both instruments, wh

248 Plating SCN neurons at <100 cells/mm(2) eliminated synap

249 Finally, plating significantly prolonged operative duration by 20

250 Serial-dilution plating, single-cell fluorescence microscopy, and flow-c

251 e number of cells at the edge of colonies by plating small colonies can increase differentiation effi

252 edetermined composition of the metal mixture plating solution (and hence the nanowire composition).

253 e optimised design focused on increasing the plating solution flow to avoid sedimentation, and as a r

254 ll with the composition of the metal mixture plating solution, indicating a reproducible plating proc

255 g different types of template and by varying plating solvent composition.

256 ral assemblages often dominated by domed and plating species of the genera Agaricia, Porites and Side

257 ion of striped nanowires based on sequential plating steps from different metal solutions and leads t

258 the long term by repeated re-sorting and re-plating steps.

259 metallic Li through in situ monitoring of Li plating-stripping processes.

260 ation, and stable cycling performance for Mg plating/stripping and Mg insertion/de-insertion in a mod

261 aller impedance and excellent stability upon plating/stripping cycles compared to cells using bare ga

262 ibutes toward the understanding of potassium plating/stripping electrochemistry and paves the way for

263 e of potassium enabling reversible potassium plating/stripping electrochemistry with high efficiency

264 ng of this composite electrode with small Li plating/stripping overpotential (<90 mV) at a high curre

265 controlled lithium deposition during lithium plating/stripping results in low Coulombic efficiency an

266 Although plating studies showed that the yeast were still [PSI+],

267 Plating suspended Swiss 3T3 cells onto fibronectin-coate

268 separation of the lanthanides, the molecular plating technique was applied to prepare thin samples to

269 preparation of proper samples, by molecular plating technique, for alpha-spectrometry measurements.

270 ion, we compared broth enrichment and direct plating techniques by using brain heart infusion broth a

271 Electrochemical plating techniques were used to form quasi-reference and

272 lectrodes are modified using anodisation and plating techniques which do not require intricate and ex

273 Plating tests and PCR amplification indicated that the i

274 constructed by picking colonies from primary platings that may contain single or multiple microorgani

275 By plating the bacterium on medium containing the CAMP nisi

276 -ir neurons when administered at the time of plating the E14 VM cells in culture.

277 Plating the infected cells on a basement membrane matrig

278 lagenase XI, dispase and trypsin followed by plating the resultant muscle slurry on collagen type I-c

279 into an invertase-deficient yeast strain and plating the transformants on a medium containing sucrose

280 After subsequent plating, the hyaluronan-binding chondroitin sulfate prot

281 ompared to a broth preenrichment followed by plating to Baird-Parker agar.

282 in the detection of VRE than is direct fecal plating to BEA agar.

283 Direct plating to CHROMagar (BD Diagnostics) was compared to a

284 containing 2 microg/ml imipenem followed by plating to MacConkey agar (MAC) (method 1) and (ii) stre

285 , and 12-month visits and cultured by direct plating to mannitol salt agar (MSA) and CHROMagar MRSA (

286 ally mapped after CM treatment or fibroblast plating to obtain conduction velocity and action potenti

287 rospheres (10-20 microm) through electroless plating to produce bulk (i.e., gram) quantities of nanop

288 structed tumor cell streaming in vitro by co-plating tumors cells, macrophages and endothelial cells

289 nd antigen expression profile as compared to plating unfractionated CD34(+)/lin(-)-enriched bone marr

290 This study compared results from plating urine specimens with the BD InoqulA instrument u

291 However, the efficiency of plating was about 12% of that of the parent strain.

292 phenotype during the 72 hours after initial plating was coincident with progressive UPP induction.

293 ed in more than 50 industries such as chrome plating, welding, wood processing and tanneries.

294 he sensitivities of ESwab and LS upon direct plating were 93.8% and 87.5%, respectively, and increase

295 Only 8% of typical colonies from direct plating were confirmed by PCR for vvhA; others yielded n

296 c backbone enables uniform lithium stripping/plating, which successfully confines lithium within the

297 oltage is sufficiently high to avoid lithium plating while not significantly reducing cell potential.

298 Electrochemical dual-pulse plating with sequential galvanostatic and potentiostatic

299 rine specimens with the WASP was compared to plating with the Dynacon Inoculab instrument.

300 The results of duplicate plating with the same instrument (replicate plating) and