ライフサイエンスコーパス: culture media

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

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

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

4 derived neurotrophic factor were included in culture media.

5 P65 along with reduced procollagen type I in culture media.

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

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

8 ly engineered Y lipolytica and purified from culture media.

9 hich often require numerous and complex cell culture media.

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

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

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

13 ted cultures representing 7 types of aerobic culture media.

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

15 MVBs and diminished release of exosomes into culture media.

16 emonstrate through the analysis of bacterial culture media.

17 , produced detectable Klotho protein in cell culture media.

18 he genus Mycobacterium avium grown in liquid culture media.

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

20 eterminants from solid and broth Middlebrook culture media.

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

22 ensity and fluorescence during incubation in culture media.

23 ontrolled by the siRNA concentration in cell culture media.

24 urify enveloped particles directly from cell culture media.

25 urer performed protein hydrolysis for use in culture media.

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

27 decontamination, antibiotics, and different culture media.

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

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

30 due to poor survival after exposure to fresh culture media.

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

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

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

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

35 surface translocation and secretion into the culture media.

36 ly less than what is supplied in traditional culture media.

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

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

39 ased nicotine accumulation in the hairy root culture media.

40 re incubation been applied only to anaerobic culture media.

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

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

43 identification directly from positive blood culture media.

44 ased when antioxidants were removed from the culture media.

45 ected clinical specimens using only standard culture media.

46 suspicious colonies grown on selective stool culture media.

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

48 tifying bacteria and fungi recovered on agar culture media.

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

50 nd between tissues stored in the 2 different culture media.

51 MSCs and increased adiponectin levels in the culture media.

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

53 ve for microorganisms identified by specific culture media.

54 d by size-exclusion chromatography from cell culture media.

55 sence of neutralizing components in the cell culture media.

56 sts depend on the level of folic acid in the culture media.

57 hat can be readily isolated from conditioned culture media.

58 the necklace, and the improved stability in culture media.

59 s coating on nanoparticles dispersed in cell culture media.

60 e and from cell-free DNA collected from cell culture media.

61 l bla(CTX-M-14) gene, and was independent of culture media.

62 mical structure of PNA microcapsules in cell culture media.

63 od species grown in monoculture on different culture media.

64 e editing and acetate supplementation of the culture media.

65 ll proteins and other components in the cell culture media.

66 omes, derived from human body fluids or cell culture media.

67 related to the biodegradation of gelatin in culture media.

68 m the plasma samples, as well as conditioned culture media.

69 ological route due to the required bacterial culture media.

70 lemented in different salt concentrations to culture media.

71 oncentration of TNF-alpha in astrocytes cell culture media.

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

73 erences and ion suppression effects from the culture media.

74 al screening to adjust culture conditions or culture media.

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

76 main outcome measure was positive growth on cultured media.

77 e detection of lactate within embryonic cell cultures media.

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

79 at can only exist extracellularly or in cell culture media, 95% elimination of H(2)O(2) at 5-200 uM r

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

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

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

83 (2020) describe optimized culture media and a mechanical stretching regimen to pro

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

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

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

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

88 cells as well as 5-HT concentrations in the culture media and cell lysates without changing the expr

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

90 oV-2 suspended in either simulated saliva or culture media and dried on stainless steel coupons.

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

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

93 fe solution application formats such as cell culture media and human serum.

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

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

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

97 nd increased IGF1 protein levels in the cell culture media and increased cellular phosphorylation of

98 Selective fungal culture media and longer incubation periods yielded high

99 luidic-based device to isolate exosomes from culture media and patient samples.

100 Standard culture media and protocols were used to identify coloni

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

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

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

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

105 e evaporation rate of droplets consisting of culture media and the resulting changes in solute concen

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

107 ow weight percent (less than 3 wt %) in cell culture media and undergoes shear-thinning and rapid sel

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

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

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

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

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

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

114 long-chain fatty acid mixture added to cell culture media, and mass spectrometry-based metabolomics

115 pluripotent stem cell (iPSC)-derived neuron culture media, and the downregulation of gene expression

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

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

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

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

120 ction limits <1 pM in 150 mM buffer and cell culture media, as well as < 10 pM in artificial CSF.

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

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

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

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

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

126 applied (14)C-radioactivity remained in the culture media at the conclusion of the experiments, comp

127 ASCT2ko 143B cells grew well in standard culture media, but ASCT2 was required for optimal growth

128 din A treatment reduced orexin levels in the culture media, but increased it in the cell lysates.

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

130 directly in aqueous solutions such as cells culture media, but they offer much a higher on/off ratio

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

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

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

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

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

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

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

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

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

140 ropin secretion was > 4000-fold higher in ST culture media compared to TSC media.

141 tential have been limited by biomaterial and culture media compositions, as well as cellular sources.

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

143 New blood culture media containing antibiotic-binding polymeric be

144 sclerotiorum mycelial growth was reduced in culture media containing cell wall polysaccharides from

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

146 llum commune VE_07 was produced in different culture media containing pine sawdust (PS), grape residu

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

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

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

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

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

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

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

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

155 efflux induced in vitro by LDL added to the culture media either alone or together with HDL or ex vi

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

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

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

159 ta and, also, demonstrated the importance of culture media for detecting ESBL E. coli.

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

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

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

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

164 We then screened bacterial culture media for TTX using LC-MS/MS and identified TTX-

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

166 antify pyocyanin concentrations in cell-free culture media from different strains of P. aeruginosa.

167 roup and control group, the pH value of cell culture media from H460 cancer cell culture plates from

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

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

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

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

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

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

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

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

176 Numerous defined culture media have been empirically developed but never

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

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

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

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

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

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

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

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

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

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

187 Liquid culture media increase the chance of isolation of bacter

188 We analyzed culture media incubated with in vitro grown E. multilocu

189 Culture media individually deprived of each of the 20 am

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

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

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

193 Further refinement of culture media is needed to improve the quality of embryo

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

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

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

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

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

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

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

201 cate that the presence of PR and SLP in cell culture media may significantly impact in vitro studies

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

203 By culture media modifications, bovine serum albumin (BSA)

204 ts utilising nanoparticles dispersed in cell culture media monitor and report the pH of suspensions d

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

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

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

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

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

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

211 Using the culture media of human embryos with normal morphologic f

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

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

214 r upregulated miRNAs in MFS patient sera and culture media of MFS cells.

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

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

217 hCGbeta, IL-8 and TNFalpha from conditioned culture media of single human embryos using electrochemi

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

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

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

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

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

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

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

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

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

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

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

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

230 d potential mispaired side products, in cell culture media, or other complex matrices.

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

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

233 o their degradation or sequestration in cell culture media prior to analysis.

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

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

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

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

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

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

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

241 ental step comprises bright-field imaging of culture-media samples followed by automated image proces

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

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

244 1 (Csf1), the specific ligand for Csf1r, to culture media significantly enhanced the self-renewal of

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

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

247 We found that culture media supplemented with glutamine, glutamate, or

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

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

250 well as metabolites for addition to in vitro culture media that support the growth and maturation of

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

252 phenol red (PR) are ubiquitous components of culture media their effect on differentiation is largely

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

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

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

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

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

258 n from perfusion media (i.e., blood, or cell culture media) to cells within cell-dense, metabolically

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

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

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

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

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

264 DAPI released in situ in cell culture media was incorporated into retinal pigment epit

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

266 l-associated membrane protein 1 (LAMP1) into culture media was significantly attenuated.

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 The mean oxygen levels for water and cell culture media were 27.7 +/- 2.1% and 27.6 +/- 4.1%, resp

270 Cell culture media were analyzed with ultra-high-performance

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

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

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

274 Historic cell culture media were designed to ensure continuous cancer

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

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

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

278 Developed decades ago, traditional culture media were not intended to resemble the metaboli

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

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

281 n simulated saliva and every 14.3 minutes in culture media when exposed to simulated sunlight represe

282 ating on BaTiO(3) nanoparticles suspended in culture media when prepared without alteration of the pH

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

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

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

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

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

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

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

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

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

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

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

294 1 was inducibly expressed in the presence of culture media with or without added IL-1beta, IFN-gamma,

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

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