ライフサイエンスコーパス: culture medium

1 and saliva) to 3 h (in prostate cancer cell culture medium).

2 etection of Staphylococcus aureus from blood culture medium.

3 between isolates and is also depended on the culture medium.

4 rP) in a real clinical scenario such as cell culture medium.

5 h in ATL compared to that in GM17 laboratory culture medium.

6 ng a tyrosine-sulfated CCR5 peptide from the culture medium.

7 a sterile basin partially filled with tissue culture medium.

8 (ELISA) detection of the protein in the cell culture medium.

9 tudies omitted translation inhibitors in the culture medium.

10 L mounted syringe was filled with the tissue culture medium.

11 ompared to the direct infusion of Dex in the culture medium.

12 gators for method development and testing of culture medium.

13 ide HMGB1 species in serum, saliva, and cell culture medium.

14 total biotin, most of which is found in the culture medium.

15 trometry (GC-MS) analysis of cell-free spent culture medium.

16 following inoculation and incubation in cell culture medium.

17 meta-hydroxybenzoate were taken up from the culture medium.

18 calcitonin-related species released into the culture medium.

19 tor vessels and stabilized over 2-wk using a culture medium.

20 amage was determined by LDH leakage into the culture medium.

21 be prevented by buffering the Ca(2+) of the culture medium.

22 ased along with an increase in Fe(3+) in the culture medium.

23 erum concentration and buffering capacity of culture medium.

24 aining MFC by adding calcium chloride to the culture medium.

25 ase of dopamine from NG108-15 cells into the culture medium.

26 h the secretion of cleaved IL-1beta into the culture medium.

27 e surface the desorption is very weak in the culture medium.

28 lucose or glucosamine or exogenous HA to the culture medium.

29 nanocomplexes were stable in serum-free cell culture medium.

30 uced by the addition of purified BslO in the culture medium.

31 hat were detectable in cell lysates and cell culture medium.

32 ed TF-positive microparticles (MPs) into the culture medium.

33 romoted an increase in irisin release in the culture medium.

34 ss spectra of various components of the cell culture medium.

35 incubation in an oxacillin-containing liquid culture medium.

36 wth factor-4 (FGF4) and heparin supplemented culture medium.

37 e articular cartilage explants in serum-free culture medium.

38 ases in IL-10 concentration were observed in culture medium.

39 e of hES cells on PMEDSAH coating in defined culture medium.

40 , leading to release of fatty acids into the culture medium.

41 of A549 cells and are not secreted into the culture medium.

42 days after removal of cyclodextrin from the culture medium.

43 oil, which were reproducibly transferred to culture medium.

44 ere dependent on the supplement added to the culture medium.

45 n of physiologic levels of ST6Gal-1 into the culture medium.

46 olize GlcNAc provided as a supplement to the culture medium.

47 reduced by adding a human sialic acid to the culture medium.

48 pression of control bacteria grown in tissue culture medium.

49 d culture at 22 degrees C or 37 degrees C in culture medium.

50 and increases soluble fractalkine content in culture medium.

51 ies and to the release of the S layer in the culture medium.

52 y fluorochrome-labeled avidin present in the culture medium.

53 all molecule antagonists present in the cell culture medium.

54 epitaxial growth in aqueous solvent and cell culture medium.

55 (FBS) than when it was grown in the standard culture medium.

56 growth phase released 220 exosomes/cell in culture medium.

57 f non-biological origin in chips filled with culture medium.

58 ype D virus, and dimethyl sulfoxide added to culture medium.

59 TB-9 bladder cells when added exogenously to culture medium.

60 down increased MG concentration in cells and culture medium.

61 ected by the environmental osmolality of the culture medium.

62 ecreased release of progeny virions into the culture medium.

63 f nearly homogeneous gp140 directly from the culture medium.

64 DBM was lyophilized, ground, and placed into culture medium.

65 y reference strains differs depending on the culture medium.

66 alpha1(I) and mature alpha1(I) expression in cultured medium.

67 ential in simple buffer solution and in cell culturing medium.

68 Chelating divalent cations from the culture medium abolished these interactions, as did inhi

69 CCN2 protein levels, with secretion into the culture medium after APF treatment.

70 applying methylated beta-cyclodextrin to the culture medium allows the sequestration of heterologous

71 the levels of reactive oxygen species in the culture medium, along with collagen I and fibromodulin p

72 riments performed directly from the gelified culture medium also allowed us to identify a new variant

73 depended on the presence of rhamnose in the culture medium and arginine in the challenge medium.

74 ted with bacteria in different media (Zobell culture medium and artificial seawater) with or without

75 EVs were identified in fluke culture medium and bile specimens from infected hosts.

76 ucrose density gradient fractionation of the culture medium and cellular extracts suggests continued

77 shown by ELISA measurement of IL-17A in the culture medium and flow cytometric analysis of IL-17A-se

78 ion of frmRAB, detection of dimethylamine in culture medium and formaldehyde production when cell-fre

79 iron at physiological concentrations in cell culture medium and human plasma.

80 first used to isolate exosomes from the cell culture medium and human serum, respectively.

81 ncreased pyrophosphate concentrations in the culture medium and in bone, respectively.

82 Levels of cytokines in cell culture medium and in GCF were measured by Luminex over

83 ed extracellular reelin concentration in the culture medium and increased phosphorylation of the down

84 nes released significantly more BPA into the culture medium and induced more cytokine production in c

85 dly increase the pH of plant suspension cell culture medium and inhibit root growth.

86 ection device was used to directly inoculate culture medium and LIM broth.

87 upregulated in abscesses and iron-restricted culture medium and negatively regulated by Fur, but only

88 sult in a loss of recombinant protein in the culture medium and no association with microfibrils.

89 ak down LPA present at substantial levels in culture medium and normal skin to generate outward-facin

90 the addition of excess exogenous iron to the culture medium and not a variety of other metals.

91 ial neuronal migration, we added BDNF to the culture medium and observed increased cell migration.

92 Soluble factors contained in culture medium and serum were measured by enzyme-linked

93 vatives are quite stable in conditioned cell culture medium and show promise for delivering drugs and

94 several bio-adaptable solutions, mainly cell culture medium and simple buffered solutions.

95 port a substantial amount of miRNAs into the culture medium and the export process is largely energy

96 o a combined effect of McC imported from the cultured medium and intracellularly synthesized antibiot

97 e microwave parasitic effects (including the cultured medium and substrate materials).

98 y oral artificial connective tissue (ACT) in culture medium, and a method to manufacture unidirection

99 ed using protein ELISAs and conditioned cell culture medium, and showed that NFATc4 siRNA reduced CXC

100 count, the absence of EF-Tu and SecA in the culture medium, and the lack of effect of autolysin-defi

101 creased salt concentrations in the bacterial culture medium, and, concordant with the in vitro result

102 In the presence of adipocyte-conditioned culture medium, anticontractile effects of the adipose t

103 regulation of a subset of genes in standard culture medium are maintained throughout at least 80% of

104 r background levels of this compound in cell-culture medium are sufficient to up-regulate CYP1A1 mRNA

105 ng the release of adenylate kinase (AK) into culture medium as a reporter of yeast cell lysis.

106 sed on HPLC analysis of cell lysates and the culture medium, as well as cell-free experiments with ur

107 tissues were preserved for 7 days in tissue culture medium at 31 degrees C.

108 ared to bacteria grown in a conditioned cell culture medium at 37 degrees C to identify genes that we

109 ferentiation are often added directly to the culture medium at fixed concentrations and effects are u

110 uffered saline (PBS, oligotrophic) and basal culture medium (BCM, eutrophic).

111 rve with the concentration of glucose in the culture medium being varied across 42 wells of a 96-well

112 In the culture medium BG-11 amended with 250 muM Ca and 50 or 2

113 II inhibitors, guided by measurement of cell culture medium binding, revealed the structure-activity

114 ion of uric acid to cells grown in a defined culture medium, but only when molybdate (Mo) and selenit

115 cally enhanced C3 (but not C5) production in culture medium by 9.8- or 7.1-fold, respectively.

116 sence of selenocyanate in Chlorella vulgaris culture medium by electrospray mass spectrometry, based

117 COOH-terminal fragment is released into the culture medium by SubA treatment, and COOH-terminal doma

118 approximately 100 kDa, respectively, in the cultured medium by Western blot analysis.

119 ude of daily temperature fluctuations in the culture medium can be drastically reduced, while maintai

120 en and glucose deprivation, conditioned cell culture medium collected after CORM-3 treatment enhanced

121 reased acidification of HCO(3)(-)-containing culture medium compared with cells expressing vector alo

122 more prone to degradation in EXT1(-/-) mESCs culture medium compared with that of wild type cells.

123 entiation; specific depletion of TH from the culture medium completely blocked terminal erythroid dif

124 Blood serum, a common cell culture medium component, is replete with EVs and must b

125 The protocol is based on a selective culture medium comprising both mitogens (forskolin and o

126 dent upon in vivo exposure of mouse uteri to culture medium conditioned by low-quality human embryos.

127 ion that varies with the drug concentration, culture medium conditions, and bacterial species tested.

128 The substrate was then immersed in the culture medium containing drug for 2 days.

129 biosensing technique in the presence of cell culture medium containing fetal bovine serum (FBS), whic

130 The exogenous addition of culture medium containing Mcc(ia) or purified in vitro-g

131 er se but is added to the cells via the cell culture medium containing serum or serum-derived compone

132 us type 1 (HSV-1) in detergents-treated cell culture medium containing various serum concentrations w

133 h varicella-zoster virus (VZV), and the cell culture medium contains no infectious virus.

134 n both sonicated bacteria and B. burgdorferi culture medium contribute to type I IFN-responsive gene

135 ficantly, cholesterol supplementation of the culture medium corrects the elongation and migration def

136 s were isolated and incorporated into tissue culture medium, cotton SE was promoted.

137 whether supplementation of antioxidants in a culture medium could protect immature mouse oocytes from

138 We found that cGAMP added to the culture medium could suppress the replication of the hep

139 ncreased as the glucose concentration in the culture medium decreased, and this finding did not match

140 and the levels of mutant HTT released to the culture medium decreased.

141 albumin at physiologic concentration in the culture medium did not abolish the effect of IS.

142 Since the conductivity of the culture medium did not change after the addition of CaCl

143 ures treated with ceftriaxone, the pH of the culture medium did not change through day 56, whereas it

144 PC by supplementation of 20:4-PC to the cell culture medium diminished Akt [serine (Ser)473] phosphor

145 llected from Emb-LPD mothers within standard culture medium displayed enhanced TE endocytosis compare

146 of ATP or the enzymatic depletion of ATP in culture medium does not modulate viral fusion.

147 -well plates (1 x 10(4) cells/well) in plain culture medium (Dulbecco's modified Eagle's medium [DMEM

148 ow that EndA molecules are secreted into the culture medium during the growth of pneumococcal cells,

149 ine serum (FBS), which is commonly used as a culture medium during vaccine production.

150 40 (Zn(2+)-Abeta40) oligomers formed in cell culture medium exhibit quasi-spherical structures simila

151 osinase into exosomes and secretion into the culture medium, explaining the hypopigmentation in OCA-4

152 ignificant enrichment of diterpenoids in the culture medium, fast-growing adventitious root cultures

153 mately 66% of the wild-type growth rate in a culture medium featuring lipid as the only carbon source

154 o robustly increased in neuronal lysates and culture medium following lithium-VPA co-treatment.

155 y challenged by more than 10(9) cells mL(-1) culture medium for 30 d.

156 porcine hearts were dissected and placed in culture medium for 72 hours before infection with C. pne

157 oidal solutions in aqueous solution and cell culture medium for biological applications.

158 chromogenic medium, to conventional primary culture medium for evaluation of urine specimens.

159 Using serum-free fully-defined culture medium formulations, we measured synthetic, deto

160 HC) cells were incubated with [(14)C]MTHF in culture medium from 30 min to 2 h, and uptake of radiotr

161 addition of recombinant RANKL to conditioned culture medium from Akt1-deficient osteoblasts.

162 Furthermore, the culture medium from PAR-2-treated pancreatic cancer cell

163 Culture medium from pellets contained high molecular wei

164 In some studies, the cultured medium from mesenchymal stem cells has been as

165 group 2 (critical limb ischemia treated with culture medium), group 3 (critical limb ischemia treated

166 ia-reperfusion injury with intravenous fresh culture medium; group 3: Ischemia-reperfusion injury wit

167 lytical variables were also assayed, such as culture medium, growth temperature, and use of serial su

168 thal; the presence of purified Dtx or Stx in culture medium has no effect on predator viability.

169 retion of T3SS2 effectors into the bacterial culture medium; however, it is essential for transfer of

170 as observed, both in cell extracts and spent culture medium (i.e. tumor cell-free but mycoplasma-cont

171 nalyses showed that addition of galactose to culture medium improves total oxidative capacity of the

172 s were stapled in parallel, directly in cell culture medium in 96-well plates, and simultaneously eva

173 ivo, removing it whole and perfusing it with culture medium in a microfluidic device.

174 ace of a Petri dish, and then immersed under culture medium in which cells are suspended.

175 Accumulation of SZP in the culture medium, in response to hedgehog proteins (sonic

176 A culture medium, in which gliadins were the sole source o

177 Finally, rCASP6-activated microglial culture medium increased EPSCs in spinal cord slices via

178 Furthermore, conditioned podocyte culture medium increased glomerular transendothelial alb

179 Here we show that maintaining PEG in culture medium increases the rate of infection by at lea

180 cult because of the quick evaporation of the culture medium inside the reactors.

181 system to extract aldosterone from the cell culture medium into organic solvent enabled the developm

182 ced by high-concentration ascorbate and cell culture medium iron efficiently kills cancer cells.

183 Cell culture medium is a critical factor for hPSC to maintain

184 The density of the culture medium is chosen such that the bacteria initiall

185 When cell culture medium is deprived of threonine, ES cells rapidl

186 uggests that exposure of virions to the cell culture medium is obligatory during spread in epithelial

187 n the adherent cells are at low density, the culture medium is responsible for coordinating cell divi

188 nd cell debris, a 0.50 mL sample (e.g., cell culture medium) is incubated with CM-Dil dye to fluoresc

189 [(13)C]Itaconate in the cell culture medium leads to elevated intracellular levels of

190 ontinued to show satisfactory performance in culture medium (linear range to 2 mM, dynamic range to 7

191 acid, and reduction of ascorbic acid in the culture medium mimicked the osteoclastogenic effect of l

192 The coordination and structure of 1 in cell culture medium (minimum essential medium, MEM) and fetal

193 dditionally, depletion of cholesterol in the culture medium mitigated the inhibitory effects of mutan

194 Neither the tissue culture medium nor a homogenate prepared from VZV-infect

195 Supplementation of recombinant LTBP-2 in culture medium not only rescued the microfibril meshwork

196 attributable to dimethyl sulfoxide (DMSO) in culture medium, NTCP overexpression, and HBV genotype D.

197 tion, we confirmed that acidification of the culture medium occurs independent of the availability of

198 phase, was discovered and purified from the culture medium of Bacillus cereus, Bacillus anthracis, a

199 heir MTs after air exchange above the static culture medium of biofilms.

200 d hepatitis E virions were released into the culture medium of both cell lines.

201 opied by adding monomeric alphaS to the cell culture medium of control pMac.

202 the neoepitope Ser77 were released into the culture medium of cytokine (TNF-alpha and IL-6/soluble I

203 Exosomes were isolated from the culture medium of drug-treated donor cells (Donor cells)

204 To do this, we purified exosomes from culture medium of eosinophils and characterized them.

205 oth effects prevented by the addition in the culture medium of FGF21 in a concentration-dependent man

206 n both in the pericellular matrix and in the culture medium of HaCaT cells.

207 Addition to culture medium of IL-6 and TGF-beta1 caused more activat

208 AHCC was added to the culture medium of intestinal epithelial cells (IEC18 and

209 t that when isoleucine is withdrawn from the culture medium of intraerythrocytic P. falciparum, the p

210 e in bronchoalveolar lavage fluid (BALF) and culture medium of lung epithelial cells.

211 When added in the culture medium of mammalian cells, PB1-F2 amorphous aggr

212 mbinant TSG-6 (TNF-stimulated gene-6) to the culture medium of murine airway smooth muscle (MASM) cel

213 Supplementation of the culture medium of the heme-auxotrophic SCV with heme, bu

214 However, NAR accumulation in the culture medium of these cells was only detectable under

215 ing glucose concentration (up to 46%) in the culture medium of Volvariella volvacea resulted in a not

216 es were either treated with EMD dissolved in culture medium or added to wells/inserts precoated with

217 homeostasis in vitro or in vivo by analyzing culture medium or blood.

218 ory cells from liquefied sputum samples to a culture medium or buffer solution is a critical step bec

219 e influenced by the nutrients present in the culture medium or by the utilization of endogenous store

220 viral spreading of US28-deficient HCMV, via culture medium or cell-to-cell transmission, was signifi

221 o use either feeder cell, serum, conditioned culture medium or embryoid body, methods that cannot avo

222 Indeed, increasing the buffering capacity of culture medium or frequency of media replacement partial

223 mporal resolution PDGF that is added in cell culture medium or secreted by neighbouring cells.

224 Depletion of threonine from the culture medium or threonine dehydrogenase (Tdh) from mES

225 ival did not differ with respect to age, MSC culture medium, or dose of MSCs delivered.

226 C3 accumulated in mast cell culture medium over time and by 3 d reached a concentrat

227 Interestingly, CPEC-conditioned SMC culture medium promoted EC proliferation and migration b

228 e demonstrate that T. congolense-conditioned culture medium promotes T. brucei stumpy formation in vi

229 on of lactate in a commercial embryonic cell culture medium providing excellent agreement between the

230 assessed in phosphate-buffered saline, cell culture medium, rat serum, and cellular lysate, and resu

231 er, supernatants from r-HuBDNF-activated EGC culture medium, rather than r-HuBDNF alone, triggered ma

232 ition of geranylgeranyl pyrophosphate to the culture medium restored actin stress fiber organization

233 les compared with that detected in bacterial culture medium, resulting in an underdetection of fungi

234 A new culture medium (RGM medium) for the isolation of rapidly

235 e of <10 kDa from S. epidermidis conditioned culture medium (SECM), but not similar preparations from

236 relationship between selenium levels in the culture medium, selenoprotein expression, and replicativ

237 Pulldown experiments from adult parasite culture medium showed that rFhKT1 interacts specifically

238 Experiments with cell culture medium showed that virus inactivation by deterge

239 decreases soon after they are transferred to culture medium, showing that generation of the shorter i

240 findings show that the presence of WNT3A in culture medium significantly promotes myogenic commitmen

241 Lactate levels in the culture medium starting from 50microM with production ra

242 tion of norepinephrine or epinephrine to the culture medium stimulated ghrelin secretion, and this ef

243 urce of bacteria) was plated on an AHG-based culture medium, strains with gliadinase activity were is

244 es with reduced structures were found in the culture medium, suggesting that cells are able to transp

245 eus predominantly accumulates acetate in the culture medium, suggesting that the phosphotransacetylas

246 ts of intestinal layers were cultivated with culture medium supplemented with growth factors and anti

247 ventricular zone were propagated in vitro in culture medium supplemented with IGF-II analogs.

248 y in these cells, and copper addition to the culture medium suppressed these biochemical defects.

249 e DCs with a sustained release of CsA to the culture medium, suppressing alloreactive T-cell prolifer

250 ormation is more strongly suppressed in cell culture medium than in aqueous buffer.

251 on of lipolysis in the absence of BSA in the culture medium that acts as a fatty acid scavenger.

252 Here we develop a cell culture medium that enables us to routinely establish ce

253 esence of AGS cells or in purine-free tissue culture medium that has been conditioned by AGS cells in

254 A caused an increase in ATP concentration in culture medium that was abolished by preincubation with

255 o exhibit increased cytotoxicity in PC3 cell culture medium that was already below pH 7.0 at the time

256 On removal of serum and insulin from the culture medium, the morphological characteristics of the

257 placed in a vacuum filtration setup to pull culture medium through the microdevice, trapping the cel

258 Increasing the osmolarity of the culture medium to 800 mOsm extended CLN3 distribution aw

259 n water, phosphate-buffered saline, and cell culture medium to afford tough hydrogels capable of with

260 (Ca), phosphorous (P) and proteins from cell culture medium to anatase nanoparticles that are extreme

261 the construct and pumped with nutrient-rich culture medium to supply nutrients to the cells and remo

262 We found that iron depletion from the culture medium triggered expression of the ferrous iron

263 e transgenic plant lines grown in hydroponic culture medium, two expressing monoclonal antibodies Guy

264 kill for all strains 6 hours, regardless of culture medium used.

265 e to quantify 20 muM of fluorouracil in cell culture medium using a standard FTIR instrument, while i

266 gative bacteria directly from positive blood culture medium using the Bruker MALDI Biotyper and to ra

267 re by direct nanoparticle suspending in cell culture medium was also performed as control.

268 GDNF protein content in cells and in culture medium was analyzed by enzyme-linked immunosorba

269 The cell culture medium was assayed for the presence of the fluor

270 ibitors of MMPs (TIMPs) 1, 2, and 4 into the culture medium was assessed using enzyme-linked immunoas

271 The majority of TF protein in the culture medium was associated with MPs.

272 brain extract from aged APP tg mice and the culture medium was continuously supplemented with synthe

273 limit of detection of yeast species in blood culture medium was determined to be 5.9 x 10(5) CFU, wit

274 at the P content in bacteria grown in +As/-P culture medium was far below the quantity needed to supp

275 The level of VEGF protein in the culture medium was measured by ELISA.

276 When the DCCM-1 cell culture medium was separated into its small molecule sol

277 silica-titania), when the serum level of the culturing medium was 0.0-0.01%.

278 Using an enriched culture medium, we established and characterized 11 MCC

279 he method, 19 samples from two human embryos culture medium were analyzed by high-pressure liquid chr

280 d SDC4 and sulfated glycosaminoglycan in the culture medium were increased by 52 and 65%, respectivel

281 The cytokines in the culture medium were measured by ELISA.

282 content in myotubes and GDNF in conditioned culture medium were quantified by enzyme-linked immunoso

283 plasma under venous shear in iron-free cell culture medium were significantly more susceptible to an

284 mic conditions nor the absence of insulin in culture medium were sufficient to promote cell death.

285 Odorant aglycones released in the culture mediums were isolated and analysed by HS-SPME-GC

286 ld-type rF70K and rFN were secreted into the culture medium, whereas all mutant proteins were either

287 -positive samples were detected in bacterial culture medium, whereas greater rates of detection for f

288 psilonRI did not affect C3 protein levels in culture medium, whereas incubations with PMA, TNF-alpha,

289 d particles (38-100%) was observed in Zobell culture medium, which may be related to nutrient availab

290 ked to stimulatory/inhibitory factors in the culture medium, which ultimately affect cell growth.

291 Ca(2+) was removed, then reintroduced to the culture medium while IP and TER readings were taken.

292 Supplementation of culture medium with 2 mM ascorbate reductant was inhibit

293 Treatment of the culture medium with anti-TGF-beta Ab or TGF-beta inhibit

294 Supplementation of culture medium with Neu5Ac stimulated expression of IL-6

295 Here, we developed a culture medium with polar metabolite concentrations comp

296 Supplementation of the epithelial cell culture medium with pyruvate allowed the glycolysis muta

297 Supplementation of the culture medium with synthetic autoinducing peptide (sAIP

298 Supplementation of the culture medium with the KLB ligand FGF19 had a similar e

299 for their abilities to alkalinize suspension culture medium, with synthetic SnHypSys I demonstrating

300 iated with an increase in TIMP-3 in the cell culture medium without a change in TIMP-3 mRNA expressio