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 romoted an increase in irisin release in the culture medium.

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

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

5 oil, which were reproducibly transferred to culture medium.

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

7 all molecule antagonists present in the cell culture medium.

8 epitaxial growth in aqueous solvent and cell culture medium.

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

10 ression of the plc2 gene was not detected in culture medium.

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

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

13 down increased MG concentration in cells and culture medium.

14 ected by the environmental osmolality of the culture medium.

15 ecreased release of progeny virions into the culture medium.

16 f nearly homogeneous gp140 directly from the culture medium.

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

18 y reference strains differs depending on the culture medium.

19 etection of Staphylococcus aureus from blood culture medium.

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

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

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

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

24 iffer in stability at 37 degrees C in tissue culture medium.

25 a sterile basin partially filled with tissue culture medium.

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

27 8 days postinoculation compared to growth in culture medium.

28 tudies omitted translation inhibitors in the culture medium.

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

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

31 gators for method development and testing of culture medium.

32 n-alpha-O-glycans that are secreted into the culture medium.

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

34 sitive controls overexpressed into the HNSCC culture medium.

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

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

37 following inoculation and incubation in cell culture medium.

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

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

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

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

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

43 erum concentration and buffering capacity of culture medium.

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

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

46 in the BBB to incorporate ecdysone from the culture medium.

47 ts on six Daphnia species using a soft water culture medium.

48 loped to stabilize the nanoparticles in cell culture medium.

49 at the microliter scale in a mammalian cell culture medium.

50 protein fragments, some originating from the culture medium.

51 1,000-fold more than that of the drug in the culture medium.

52 mate of the PCB levels in the cells and cell culture medium.

53 of the 2-carbon unit back to acetate of the culture medium.

54 ndogenous murine soluble TNF secreted to the culture medium.

55 (6.1%) are at time of this analysis still in culture medium.

56 ically active, monomeric s-DAB-IL-2 into the culture medium.

57 l growth phase released 220 exosomes/cell in culture medium.

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

59 calcitonin-related species released into the culture medium.

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

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

62 and placed in a well plate containing organ culture medium 1 without dextran.

63 PCBs were present in the cell culture medium (60.7-88.8%), cells (8.0-14.6%), and dish

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

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

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

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

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

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

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

71 tact shed cilia that could be recovered from culture medium and contained both membrane and axoneme p

72 By refining the experimental culture medium and creating an environment conducive to

73 control, and protein Exl1 can be observed in culture medium and during plant infection.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

91 human vascular endothelium and perfused with culture medium, and a porous membrane separating the two

92 n ectonucleotidase inhibitor were applied in culture medium, and hDPSC survival and proliferation wer

93 characterized the oxygenation of water, cell culture medium, and human blood in the FABRICA as functi

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

95 of nutrients and oxygen from the surrounding culture medium, and their consumption by tumour cells, c

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

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

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

99 reotide conjugates were found stable in cell culture medium as well as noncytotoxic in HeLa cells, an

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

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

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

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

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

105 corneas, 5 pairs each, were stored in organ culture medium before deswelling either at 31 C or at ro

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

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

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

109 ld (p <= 0.0001), while increasing CX3CL1 in culture medium by 5.8-fold (p <= 0.0001).

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

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

112 SP and IL-1beta levels were assayed in the culture medium by ELISA.

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

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

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

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

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

118 Krox20 and myelin basic protein (MBP) in SC culture medium containing dBcAMP/NRG1, which induced dif

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

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

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

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

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

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

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

126 suggesting that molecular analysis of embryo culture medium could assist in non-invasive single embry

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

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

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

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

131 to IL-6 detection using blood serum and cell culture medium demonstrates that FAIRS can quantify IL-6

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

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

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

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

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

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

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

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

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

141 40 (Zn(2+)-Abeta40) oligomers formed in cell culture medium exhibit quasi-spherical structures simila

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

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

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

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

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

147 We elucidate the significance of this new culture medium for chronic disease modeling of IL-13-ind

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

149 ile duct slices were incubated in oxygenated culture medium for up to a week.

150 This novel approach to culture medium formulation could help define the optimal

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

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

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

154 Culture medium from pellets contained high molecular wei

155 Removal of glucose from tissue culture medium further enhanced these phenotypes and, in

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

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

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

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

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

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

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

163 ion in vitro (IVF), but the available embryo culture medium in the current method is only a few micro

164 nd the secretion of surfactant into the cell culture medium in the organoids of lentiviral infected c

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

166 ly, we generate a minimal chemically-defined culture medium in which IGF1 together with Activin maint

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

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

169 Furthermore, conditioned podocyte culture medium increased glomerular transendothelial alb

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

171 olymers increasing the bulk viscosity of the culture medium independently of polymer molecular weight

172 Pure L. murinus conditioned culture medium inhibited growth and reduced the extensio

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

174 Compared to conventional culture medium, insulin-supplemented culture medium prov

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

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

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

178 measurement of growth factors released in a culture medium is considered to be an attractive non-inv

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

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

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

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

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

184 g these simple structural elements into a 3D culture medium made from packed microgels, creating a me

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

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

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

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

189 ich are predicted to be lipoproteins, in the culture medium of an ETBF strain.

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

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

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

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

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

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

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

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

198 efore used to measure alpha-synuclein in the culture medium of human brain organoids generated from n

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

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

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

202 aluated by quantifying TNF-alpha in the cell culture medium of lipopolysaccharide stimulated and non-

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

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

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

206 ection of the growth factor from each embryo culture medium of such a small concentration hence remai

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

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

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

210 impact of reduced nutrient concentrations in culture medium on mouse embryo development, metabolism,

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

212 EV isolations by precipitation from basal culture medium or apical surface wash were characterized

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

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

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

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

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

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

219 Giardia did not grow in spent cell culture medium or when separated by a permeable membrane

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

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

222 We found that in culture medium plc1 gene expression increased with incre

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

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

225 ntional culture medium, insulin-supplemented culture medium provides no additional benefit in preserv

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

227 interaction by the addition of biotin to the culture medium rapidly dissociates the motor construct f

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

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

230 The addition of manganese in culture medium restored ROS resistance in both the toxR

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

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

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

234 In cell culture medium, serum increased the rate of CVB3/28 conv

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

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

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

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

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

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

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

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

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

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

245 The addition of fatty acids to culture medium suppressed this signal, which required an

246 lls and that, in the absence of R-spondin in culture medium, taste bud cells are not generated ex viv

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

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

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

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

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

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

253 er, by direct addition of alphaSyn PFFs into culture medium, the formation of misfolded alphaSyn incl

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

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

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

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

258 The nanoparticles were characterized in cell culture medium to assess how their physical properties a

259 dium modified from an established plant cell-culture medium to nourish detached leaves laid atop it w

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

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

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

263 The osmotic pressure of GBM cell culture medium was adjusted using sodium chloride or wat

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

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

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

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

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

269 y proteins, miR-144 treated endothelial cell culture medium was subjected to proteomic analysis inclu

270 plication and/or survival only when the cell culture medium was supplemented with nonessential amino

271 The artificial culture medium was tested with two herbivorous mite spec

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

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

274 Using an insulin-supplemented culture medium, we prolong the small airway contractilit

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

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

277 esonance (NMR), the metabolic changes in the culture medium were measured in glial cells.

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

279 ytosis and the addition of serum to the cell culture medium were required for thapsigargin-mediated N

280 Production and release of CTGF in culture medium were significantly augmented in human emb

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

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

283 e), while its decomposition products in cell culture medium were ~8-fold less toxic.

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

285 Further, enzyme-loaded exosomes/EVs added to cultured medium were taken up by recipient cells.

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 (MHB) and a 64-fold lower MIC in this tissue culture medium with 20% human serum.

292 media, AZM had a 16-fold lower MIC in tissue culture medium with 5% Mueller Hinton broth (MHB) and a

293 -alpha, from an individual droplet of embryo culture medium with a bead-based digital microfluidic ch

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 stodes was different from parasite-incubated culture medium with respect to the abundance, but not th

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

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

300 ect detection of EVs in human serum and cell culture medium without tedious sample preparation was de