ライフサイエンスコーパス: culture media

1 [HEY]) and liquid (Bactec 12B and para-JEM) culture media.

2 ensity and fluorescence during incubation in culture media.

3 ontrolled by the siRNA concentration in cell culture media.

4 urify enveloped particles directly from cell culture media.

5 urer performed protein hydrolysis for use in culture media.

6 h factor beta-1 (TGF beta-1) addition to the culture media.

7 decontamination, antibiotics, and different culture media.

8 ls exposed to mammary tumor-conditioned cell culture media.

9 n skin explants and by exogenous TGFbeta1 in culture media.

10 mode of transmission, and its poor growth on culture media.

11 decreased the levels of NO and PGE2 in cell culture media.

12 nce swabs that were missed by both selective culture media.

13 d PML expression relied on IL6 secreted into culture media.

14 minus that has been purified from plasma and culture media.

15 surface translocation and secretion into the culture media.

16 y the addition of recombinant cysSA into the culture media.

17 d from porcine trabecular meshwork (TM) cell culture media.

18 ased nicotine accumulation in the hairy root culture media.

19 re incubation been applied only to anaerobic culture media.

20 ted from crude cell lysates or purified from culture media.

21 s long-term growth of hES cells in different culture media.

22 identification directly from positive blood culture media.

23 ased when antioxidants were removed from the culture media.

24 ected clinical specimens using only standard culture media.

25 suspicious colonies grown on selective stool culture media.

26 d to the levels of purine nucleotides in the culture media.

27 erences and ion suppression effects from the culture media.

28 tifying bacteria and fungi recovered on agar culture media.

29 levels of or adding exogenous agents to the culture media.

30 MSCs and increased adiponectin levels in the culture media.

31 ar domain is released into the tear fluid or culture media.

32 tubes) and solid (Herrold's egg yolk medium) culture media.

33 igands induced the release of c-Met into the culture media.

34 al screening to adjust culture conditions or culture media.

35 lagen production by Western blot analysis of culture media.

36 (189), whether or not EMD was present in the culture media.

37 Abeta that appear both in cell extracts and culture media.

38 whereas their growth was normal in standard culture media.

39 be detected as secreted proteins in the cell culture media.

40 retion of TNF-alpha and CCL20/MIP3alpha into culture media.

41 ylceramide and an increase of sterols in the culture media.

42 stimulated an early release of BDNF into the culture media.

43 d S100A4/Mts1 protein in hPA-SMC lysates and culture media.

44 to murine macrophages with Amplex Red in the culture media.

45 gnificantly as allopregnanolone was added to culture media.

46 ically stimulated by amelogenin added to the culture media.

47 in 24 hours of drug withdrawal from the cell culture media.

48 elated positively with the osmolarity of the culture media.

49 rivatized free amino acids in mammalian cell culture media.

50 G1 domain (G1-NITEGE(373)), and HA into the culture media.

51 f hypertrophy in the milieu of hyperglycemic culture media.

52 cent AFB smear, SMF, Xpert MTB/RIF, and MGIT culture media.

53 metabolized and released by Caco-2 cells in culture media.

54 ed from human lymphoblastoid cell line (LCL) culture media.

55 derived neurotrophic factor were included in culture media.

56 tor (FR) and an FR+ cancer cell line (KB) in culture media.

57 gly coupled to the host-virus dynamic in the culture media.

58 ly engineered Y lipolytica and purified from culture media.

59 hich often require numerous and complex cell culture media.

60 ply adding the fluorogenic probe to the cell culture media.

61 pyramidal tip, is also very sensitive to the culture media.

62 reducing agent) is a common additive to cell culture media.

63 ted cultures representing 7 types of aerobic culture media.

64 complex samples such as horse serum and cell culture media.

65 MVBs and diminished release of exosomes into culture media.

66 emonstrate through the analysis of bacterial culture media.

67 , produced detectable Klotho protein in cell culture media.

68 he genus Mycobacterium avium grown in liquid culture media.

69 e on-line measurement of metabolites in cell culture media.

70 eterminants from solid and broth Middlebrook culture media.

71 acConkey agar, Chocolate agar and Blood agar culture Medias.

72 main outcome measure was positive growth on cultured media.

73 e detection of lactate within embryonic cell cultures media.

74 In cell culture media, 24-hour exposure to 0.25 to 0.5 mmol/L DE

75 After removal of the inhibitor from culture media, a growth curve inflection point at 3.1 h

76 results suggest that a low glucose supply in culture media activates an apoptosis mediator and marked

77 In contrast, the addition of poly(I-C) to culture media activates the IFN-beta promoter and result

78 actor (CNTF; n = 9) or 2) allowed to grow in culture media alone (n=7).

79 HMGB1 purified from cells grown in culture media alone only minimally increased cytokine pr

80 vivo intradermal microdialysis combined with culture media analysis provides an effective, skin-spari

81 VII collagen was readily detectable in cell culture media and also localized to the dermal-epidermal

82 performed for strains cultured on different culture media and analyzed using different instrumental

83 The bioconjugate is stable in cell culture media and at neutral pH but undergoes hydrolysis

84 itrite, ascorbate, ammonia, etc.) present in culture media and biological fluids.

85 strategies for isolating EVs from both cell-culture media and body fluids, and procedures for quanti

86 anscriptase activity and HIV-1 p24 levels in culture media and cells showed that such endosomal drug

87 n of intracellular ammonia released into the culture media and contributes to alkalinity of the exter

88 essed prostatic secretions (EPS) on enriched culture media and direct microscopic observation of thes

89 ustry to have tools to characterize the cell culture media and evaluate its impact on the cell cultur

90 In addition, Dex was assessed in culture media and extracts from stratum corneum, epiderm

91 this transformation can be conducted in cell culture media and in the presence of cells by addition o

92 able under physiological conditions, in cell culture media and in tissue samples.

93 BMP1 prodomain-BMP4 complexes exist in cell culture media and in tissues.

94 al susceptibility testing is demonstrated in culture media and in urine with clinical bacterial isola

95 Selective fungal culture media and longer incubation periods yielded high

96 )Cl]- (4), a cisplatin species that forms in culture media and probably also in blood.

97 Standard culture media and protocols were used to identify coloni

98 rom the ER to the cell membrane and into the culture media and significantly improved cell viability.

99 ced in paired BACTEC Plus and BacT/Alert FAN culture media and studied simultaneously, consecutively,

100 ng the influence of E. coli bacterial hosts, culture media and the impact of either PelB or DsbA sign

101 of shed TNFalpha, TGFalpha, and sMet in cell culture media and the phosphorylation of ERK1/2.

102 can be influenced by the composition of the culture media and the presence of polyamidoamines.

103 nidia were allowed to form mycelia in tissue culture media and then harvested for DNA extraction.

104 method, we investigated the effects of four culture media and tissue harvesting sites on explant att

105 ifferentiation of three bacterial species in cultured media and spiked human urine samples.

106 er of physiological buffers and fluids, cell culture media, and bacterial broth by the Griess assay,

107 oduced during immuno-editing process in cell culture media, and could reveal that Trp consumption and

108 d fraction generated by mixing COREXIT, cell culture media, and DWH oil (CWAF).

109 temperatures (95 and -78 degrees C), in cell culture media, and in aqueous H2O2 solutions.

110 le in physiological saline solution and cell culture media, and is not cytotoxic.

111 of recombinant acid sphingomyelinase to the culture media, and the corrected sperm also had an enhan

112 e better estimated by using selective fungal culture media, and this may translate to important clini

113 Antimicrobial removal devices in blood culture media are designed to remove antibiotics from th

114 in the compositions of the conditioned cell culture media are likely contributing to different fluor

115 ration in proximal microchannels filled with culture media are precisely regulated by molecular diffu

116 he development of the assay, which uses cell culture media as a sample matrix and has a linear dynami

117 phil viability is maintained for 20 hours in culture media at 37 degrees C under anoxic conditions wi

118 l for 15 h when maintained in an appropriate culture media at 4 degrees C.

119 d chondroitin sulfate were added to the cell culture media at hyperphysiological concentrations (0.2

120 e the levels of glutamine in standard tissue culture media at least ten-fold higher than other amino

121 uman macrophages were exposed to custom cell culture media at pH 7.5-6.0.

122 revented by the presence of IFN-gamma in the culture media, but not by the presence of IL-6-neutraliz

123 toxicity, of toxic species generated in cell culture media by an argon (Ar) plasma jet.

124 Here we map the landscape of existing culture media by extracting natural-language media recip

125 l ALS (fALS) mouse model, and in spinal cord culture media by means of a specific and innovative high

126 cterium tuberculosis complex (MTBC) in broth culture media by using detonation nanodiamonds (DNDs) as

127 rise of temperature increased soluble EPS in culturing media by means of extraction from kefir grain

128 ensities in the presence of conditioned cell culture media can be used to distinguish between prostat

129 f rectal surveillance swabs on two selective culture media, CHROMagar extended-spectrum-beta-lactamas

130 espective proteins from LGG-conditioned cell culture media (CM).

131 oatings combined with components of neuronal culture media collectively support robust attachment and

132 leased five times more ASM activity into the culture media compared with nontransduced NPCs.

133 ibroblast and immortalized keratinocyte cell culture media, confirm that no simple patterns are prese

134 n donors, such as amino acids and other cell culture media constituents, at physiological pH result i

135 CEpi cells were cultured in KGM-2 serum-free culture media containing 0.15 mM calcium.

136 New blood culture media containing antibiotic-binding polymeric be

137 detected in the presence of epithelial cell culture media containing fetal bovine serum.

138 the mutant did not produce a color change in culture media containing fluorene, phenanthrene, and flu

139 Culture media containing whey (W; 2.1g/L) or whey hydrol

140 jor processed form found to be released into culture media contains a 35-residue truncation at the N-

141 more, the amount of recycled albumin in cell culture media corresponded to FcRn-binding affinity, wit

142 Engineered photonic cells dispersed in culture media could revolutionize the monitoring of cell

143 Importantly, the culture media derived from TLR2-activated Muller glia ex

144 his study identified that these two types of culture media determined differential growth of M. avium

145 Supplementing MMP-2 to culture media did not induce EMT, suggesting that EMT in

146 yol process and were incubated in three cell culture media (DMEM, RPMI-1640, and DCCM-1) to examine t

147 field and the soluble iron concentrations in culture media establishing the possibility of single cel

148 hormone analog directly from mammalian cell culture media, even when present in trace amounts.

149 defined medium F-12, but not in other tissue culture media examined, the specific components responsi

150 Viral particles from culture media exhibited morphologic features of beta-ret

151 Compound 17 was unstable in tissue culture media, failed to achieve nuclear access, and was

152 methods involve measurement of H(2)S in cell culture media following incubation with H(2)S-releasing

153 essing CD45 were generated and released into culture media for 6-7 weeks.

154 to be applied to both aerobic and anaerobic culture media for all periprosthetic specimens.

155 n stress response studies, in development of culture media for newly discovered strains, and for asse

156 side inoculation and immediate incubation of culture media for the detection of Trichomonas vaginalis

157 aerobic resin-containing (Peds Plus/F) blood culture media for the isolation of Salmonella enterica s

158 agar and chocolate agar were used as regular culture media for the microbiologic studies, whereas Sab

159 sed MPCCs to hypo-, normo- and hyperglycemic culture media for ~3 weeks.

160 n a microfluidic chip that creates arbitrary culture media formulations in 96 independent culture cha

161 gnificantly reduced the level of VEGF in the culture media from human uveal melanoma cells, mouse mel

162 ate- and (35)S-trans amino acid-radiolabeled culture media from THP-1 monocytes induced to differenti

163 Antibiotic neutralization in blood culture media from two automated systems was evaluated b

164 mycobacterial culture using liquid and solid culture media, from participants with suspected pulmonar

165 molecules inside cells and in standard cell culture media generate toxic by-products that interfere

166 In cell culture media glucose biosensor shows a sensitivity of 4

167 eatment of HBV genome-transfected cells with culture media harvested from cells transfected with each

168 poietic colony-forming units using semisolid culture media has greatly advanced the knowledge of hema

169 Numerous defined culture media have been empirically developed but never

170 V. fischeri culture media have lower osmolarities than are typical i

171 Mass spectrometry analysis of microglia culture media identified protease serine 2 (PRSS2) as a

172 generation of stable ENM suspensions in cell culture media; (ii) colloidal characterization of suspen

173 rhPRL supplementation to islet culture media improved human beta-cell-specific survival

174 lls positioned at different separations from culture media in 3D cultures.

175 The reaction of cyanide with cell culture media in 96-well culture plates reduced cyanide

176 nditions but was similar to the wild type in culture media in the absence of osmotic stress.

177 recommend inclusion of both solid and liquid culture media in the laboratory diagnosis of nonviral ke

178 roperties were measured: stability in tissue culture media in the presence of A549 lung and MCF-7 bre

179 urkat T lymphocytes in serum-containing cell culture media in the presence of the entire Jurkat secre

180 ne with those necessary to grow in different culture media in vitro, combined with isotopologue profi

181 stem (hES) cell growth in several different culture media, including commercially available defined

182 sing standard bacterial and selective fungal culture media, including Sabouraud dextrose agar with ge

183 Liquid culture media increase the chance of isolation of bacter

184 Culture media individually deprived of each of the 20 am

185 We also observed that lactate addition to culture media induced the expression of genes involved i

186 rporation from (15)N-glutamine added to cell culture media is also demonstrated and used to distingui

187 ce that the presence of ascorbic acid in the culture media is critical for overcoming the previously

188 The use of FBS in hybridoma culture media is examined here, with regards to the deve

189 of alginate overproduction observed on solid culture media is referred to as mucoid.

190 HNF1A and HNF4A and increased bile acids in culture media; it further captured multiple molecular si

191 can develop and survive in vitro, in defined culture media lacking exogenous growth factors or serum.

192 teraction with free transition metal ions in culture media leading to the generation of H2O2 and othe

193 All cells internalized cystatin C added to culture media, leading to increased intracellular cystat

194 through genetic deletion or low selenium in culture media leads to low expression of the IP3R due to

195 Evaluation of different culture media led us to discover that culturing primary

196 In analysis of cell culture media, linear calibration curves based on SEC-FD

197 we compared BD GeneOhm MRSA PCR and various culture media (mannitol salt agar with cefoxitin, MRSASe

198 atocytes were cryopreserved in suspension in culture media (Media-cryo group) or HTS (HTS-cryo group)

199 vious in vitro studies, and that common cell culture media might be unsuitable for redox research.

200 th cells, and therefore, the effects of cell culture media must be considered in the analysis of toxi

201 because many specific factors and different culture media must be used.

202 the ability of the bacteria to grow in rich culture media, mutations in each of these genes dramatic

203 lism of human cells, but neither traditional culture media nor mouse plasma mimic the metabolite comp

204 After being inoculated with culture media of cells transfected with the full-length

205 E-EVs added to the culture media of cerebrovascular pericytes were incorpor

206 cing increased the ET-1 concentration in the culture media of endothelial cells.

207 Virus released into the culture media of HCV-infected primary hepatocytes repeat

208 NS5a-positive immunofluorescence of cell culture media of IHH transfected with full-length H77 RN

209 rmed proteomics studies of HCV isolated from culture media of infected hepatoma cells to define viral

210 el of EVs in blood (P < 0.05), as well as in culture media of isolated HCs (P < 0.001) and hepatic ma

211 Like GDNF, addition of GDNF:TTC to culture media of neuroblastoma cells expressing GFRalpha

212 Exosomes were obtained from culture media of primary bronchial fibroblasts and chara

213 rmined extracellular NH2OH concentrations in culture media of several ammonia-oxidizing bacteria (AOB

214 t of surface South Pacific seawater and from culture media of the siderophore producing cyanobacteria

215 sidering current trends, the mycelia and the culture media of these mushrooms might be potential sour

216 However, in culture media of transfected cells, the p.Leu104Val solu

217 uman E-NTPDase 8 which was secreted into the culture media of transfected HEK293 cells was purified b

218 of BMI1 and PSA were performed in blood and culture-media of siRNA-transfected and non-transfected c

219 fluence of the glucose concentration in cell culture media on (18)F-FDG uptake kinetics.

220 the effects of sirolimus supplementation in culture media on human islet preparations, focusing on t

221 exogenous administration, as a component of culture media or as a transgene expressed by adoptively

222 which specimens were positive by one or more culture media or at least one CIDT and PCR were designat

223 mposed by mannitol or polyethylene glycol in culture media or by water deficit in the soil.

224 ely, typical calcium indicators are added to culture media or have low signal to noise after microinj

225 y transient transfection using standard cell culture media or serum-free media.

226 The amount of TSG-6 in culture media or SF was quantified by enzyme-linked immu

227 e myotubes were incubated in standard tissue culture media, or media supplemented with 28 mM glucose,

228 layer, and differences in cell death between culture media over the first 14 days in vitro.

229 A study of the cell culture media performed under stress conditions using fl

230 mmonly associated with the presence of >/= 2 culture media positive for growth, acute inflammation (>

231 The conditioned AEBP1(TG) macrophage culture media promoted NF-kappaB activity and survival s

232 Cheese whey culture media provided high molecular weight (>3000 kDa)

233 ressed from mammalian vectors, secreted into culture media, purified by affinity chromatography and c

234 ion and the addition of selenium to standard culture media recapitulated the effects of RM.

235 The latter failed to grow on commonly used culture media, rendering these isolates difficult to det

236 NT5A inhibitory antibody, added to UGS organ culture media, rescued prostatic budding from inhibition

237 ion of CmeABC, the presence of bile salts in culture media resulted in increased resistance of Campyl

238 Removal of TSC from culture media resulted in loss of promoter-associated po

239 Release profiles in water and tissue culture media showed that no cargo leaked when the valve

240 lidated by the analysis of VEGF-A165 in cell culture media, showing its great potential for the analy

241 1 (Csf1), the specific ligand for Csf1r, to culture media significantly enhanced the self-renewal of

242 S100A4/Mts1 in the culture media stimulated proliferation and migration of

243 can sequester active cholera toxin from cell culture media sufficient to protect intestinal cells.

244 regions, enzymatic dissociation methods, and culture media supplemented with different calcium, serum

245 esistance to nonenzymatic hydrolysis in cell culture media (t(1/2) approximately 21 days).

246 gy to efficiently formulate species-specific culture media that can easily be manipulated.

247 apture of feline calicivirus (FCV) from cell culture media that is exposed to a gold substrate modifi

248 cells in contact with hydrogel scaffolds or culture media, the diffusion coefficient can reflect int

249 Flow was controlled gravitationally to push culture media through the chamber.

250 combinant PRL (rhPRL) supplementation to the culture media to determine its potential use in the cont

251 Exposure of the cell culture media to light, temperature stress, or adventiti

252 particle sedimentation and diffusion in cell culture media to predict delivered dose values.

253 to quantify changes arising due to different culturing media to 17 tRNA families.

254 sed in the ESC-treated rats but decreased in culture media-treated rats, and border-zone function was

255 DOX per mg iron, sustained stability in cell culture media up to 7 days, and a strong r(2) relaxivity

256 mented for monitoring variations in CHO cell culture media upon exposure to high temperature short ti

257 In the same culture media used for the cytokine stimulation study, n

258 samples presented unique subtypes in the two culture media used, while 31% shared the same G-GGT alle

259 asidiomycetes were grown submerged in liquid culture media using seven different by-products of the f

260 mposition of the particles released into the culture media was analyzed.

261 The amount of cytokines in the culture media was assessed by ELISA.

262 Secretion of IL-1beta into the culture media was assessed by enzyme-linked immunosorben

263 The release of c-Met ectodomain into the culture media was determined by Western blotting using a

264 llular endothelin 1 mRNA and endothelin 1 in culture media was inhibited by supratherapeutic concentr

265 ased presence of both Tyr and melanin in the culture media was observed in treated melanocytes.

266 S and associated shifts in the osmolality of culture media was significant and prevented mouse embryo

267 Notably, the serum in the culture media was the only available source for polyunsa

268 esence, in the absence of its application in culture media, was detected in an immortalized choroidal

269 uring preadipocyte differentiation, and cell culture media were collected to analyze leptin secretion

270 Cell lysates and culture media were collected to assess apoptosis with th

271 els of AREG protein in ExeR cell lysates and culture media were confirmed by Western blot analysis an

272 is, various chalcone substrates added to the culture media were converted to an assortment of isoflav

273 SEOV RNA and infectious particles in culture media were detected in both cell types, but at h

274 TWEAK levels in culture media were determined by enzyme-linked immunosor

275 cyte chemotactic protein-1 (MCP-1) levels in culture media were measured by ELISA.

276 llular endothelin 1 mRNA and endothelin 1 in culture media were measured with Northern blots and enzy

277 L for 24h), the levels of MMP-2 and MMP-9 in culture media were significantly increased in a concentr

278 the effective cyanide concentrations in the culture media were significantly lower than reported.

279 s of growth from conventionally plated stool culture media were subjected to the OIA SHIGATOX, and re

280 somes, although isolated from unfractionated culture media, were absent in highly infectious, purifie

281 control are acetylated and secreted into the culture media, whereas lipids that pass the cycle are de

282 ivo concentration of iron to supplement cell culture media which are characterized by low iron conten

283 iffusion rates of nanoparticles suspended in culture media, which largely depend upon the effective d

284 ues; this reduces uptake of sucrose from the culture media, which leads to a repression of lateral ro

285 e found that selenium supplementation of the culture media, which resulted in a hierarchical up-regul

286 H7 only growth 50% when PBE was added to the culture media, while a slight increase on the growth of

287 ar MRSA II (CMRSAII), to that on traditional culture media with 293 stool specimens.

288 Supplementation of culture media with beta-mercaptoethanol rescues CD98hc-d

289 at least 45 chips, were detected in two cell culture media with different compositions.

290 completely rescued by supplementation of the culture media with exogenous cholesterol, while methylst

291 oma cell line Huh7.5 by supplementing tissue culture media with human serum (HS) and examined the pro

292 1 was inducibly expressed in the presence of culture media with or without added IL-1beta, IFN-gamma,

293 ro cyanide toxicity studies done in standard culture media with prolonged incubation times using gas-

294 through transgene rescue or by supplementing culture media with protease inhibitors.

295 onception) that were either 1) pretreated in culture media with the differentiating cytokine ciliary

296 Supplementing C. elegans culture media with these omega-6 PUFAs increases their r

297 in-1 could be enhanced by supplementation of culture media with uridine and N-acetylglucosamine (GlcN

298 The SCCs are soluble in cell culture media within the entire range of studied concent

299 ition, the trxB mutant was unable to grow in culture media without addition of a reductant.

300 o decompose H2O2, we grew E. coli in defined culture media without iron (M9(-)) or with ferrous ions