ライフサイエンスコーパス: fetal bovine serum

1 vant complex media (bovine serum albumin and fetal bovine serum).

2 ays are capable of effective analysis in 10% fetal bovine serum.

3 s were cultured in Medium 199 containing 10% fetal bovine serum.

4 (E)10 lenses grown in medium containing 10% fetal bovine serum.

5 es as low as 25 microM in the presence of 5% fetal bovine serum.

6 odified Eagle's medium (DMEM) containing 15% fetal bovine serum.

7 pagated in RPMI medium supplemented with 10% fetal bovine serum.

8 nse to angiotensin II, phenylephrine, and 1% fetal bovine serum.

9 human serum albumin, normal human serum, or fetal bovine serum.

10 uch as angiotensin II, phenylephrine, and 1% fetal bovine serum.

11 lls were cultured in complete or delipidated fetal bovine serum.

12 ning 2 ng/ml fibroblast growth factor and 6% fetal bovine serum.

13 ith cells incubated in medium containing 10% fetal bovine serum.

14 t a minor fraction of EDA2 was also found in fetal bovine serum.

15 rved with absorption and emission >700 nm in fetal bovine serum.

16 ation and is identical in aqueous buffer and fetal bovine serum.

17 with DMEM/F12 plus 2% B-27 supplement and 1% fetal bovine serum.

18 divide by growth factors in media containing fetal bovine serum.

19 ffered saline solution, with and without 10% fetal bovine serum.

20 um but fail to proliferate in the absence of fetal bovine serum.

21 s such as mouse-derived 3T3 feeder cells and fetal bovine serum.

22 by a single OmpG nanopore in the presence of fetal bovine serum.

23 alian cell culture systems supplemented with fetal bovine serum.

24 oin in solutions of deionized water and 100% fetal bovine serum.

25 lchitobiose is exacerbated by the removal of fetal bovine serum.

26 5pg/ml for assays containing PBS spiked with fetal bovine serum.

27 n conditioned by AGS cells in the absence of fetal bovine serum.

28 er heparin from culture supplements, such as fetal bovine serum.

29 co's minimal essential medium containing 10% fetal bovine serum.

30 lls were grown in DMEM supplemented with 10% fetal bovine serum.

31 unknown samples in both buffer and undiluted fetal bovine serum.

32 could effectively detect the exosomes in 30% fetal bovine serum.

33 ulbecco modified Eagle medium containing 10% fetal bovine serum.

34 odified Eagle's medium (DMEM) containing 10% fetal bovine serum.

35 of epithelial cell culture media containing fetal bovine serum.

36 8, or 60 hours in culture medium (M-199, 10% fetal bovine serum, 10 ng/ml epidermal growth factor, 20

37 e cultured in the presence or absence of 10% fetal bovine serum, 100 pM IGF-1, or 100 pM TGF beta.

38 0, 72, and 84 hours to medium containing 10% fetal bovine serum, 20 ng/ml fibroblast growth factor, a

39 Control was lost with fetal bovine serum, 20% oxygen, M-CSF, higher concentrat

40 osomes was investigated by incubation in 50% fetal bovine serum/50% phosphate-buffered saline, pH 7.4

41 ine-linked oligosaccharides units present in fetal bovine serum acetylcholinesterase and equine serum

42 tures of the two major oligosaccharides from fetal bovine serum acetylcholinesterase and one major ol

43 nal antibodies raised against phosphorylated fetal bovine serum acetylcholinesterase appeared to modu

44 t propidium clearly slowed the inhibition of fetal bovine serum acetylcholinesterase by all six inhib

45 , recombinant cholinesterases, and monomeric fetal bovine serum acetylcholinesterase showed a distinc

46 tennary complex type, but only the ones from fetal bovine serum acetylcholinesterase were fucosylated

47 Complexation of fetal bovine serum acetylcholinesterase with monoclonal

48 sterases (human serum butyrylcholinesterase, fetal bovine serum acetylcholinesterase, and equine seru

49 etylcholinesterase, monomeric and tetrameric fetal bovine serum acetylcholinesterase, and equine seru

50 maturity compared with glycans of monomeric fetal bovine serum acetylcholinesterase, dimeric tissue-

51 the inhibition constants with Torpedo AChE, fetal bovine serum AChE, human butyrylcholinesterase (BC

52 hosphinyloxy)-1-methylquinolinium iodide and fetal bovine serum AChE.

53 n with nutrient medium containing either 20% fetal bovine serum alone or in combination with Epothilo

54 Keratocytes cultured in fetal bovine serum also become fibroblastic, proliferate

55 in RPMI-1640 medium containing 10% (vol/vol) fetal bovine serum and 0.1 microM [75Se]selenite.

56 tem wherein alpha-MEM (supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic) was pe

57 tem wherein alpha-MEM (supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic) was pe

58 imum essential medium supplemented with 0.5% fetal bovine serum and 1% penicillin/streptomycin contai

59 nded in transwell culture in the presence of fetal bovine serum and a stable derivative of vitamin C.

60 fied Eagle's Medium (low glucose) containing fetal bovine serum and antibiotic/antimycotic.

61 osphate receptor (sIGF-II/MPR) is present in fetal bovine serum and carries mature 7.5-kDa insulin-li

62 in RPMI culture medium supplemented with 10% fetal bovine serum and characterized using morphology, h

63 Cells from old donors treated with fetal bovine serum and FGF stained positively for Ki67,

64 In the presence of fetal bovine serum and FGF, cells from old donors can pr

65 II isoforms have similar binding profiles in fetal bovine serum and have similar affinities for IGF-I

66 Activities of serum cholinesterase in fetal bovine serum and human serum were analyzed with th

67 mented with 10% unheated or heat-inactivated fetal bovine serum and incubated at 37 degrees C.

68 9) in RMPI-1640 medium supplemented with 20% fetal bovine serum and performed a Cell Death ELISA afte

69 Growth responses to fetal bovine serum and superoxide dismutase-inhibitable

70 conditioned medium required the presence of fetal bovine serum and the passage of the cells with a p

71 NA targets in the presence of complex media (fetal bovine serum) and other interfering DNA fragments

72 loproteinase, apolipoprotein E (derived from fetal bovine serum), and amastigote-specific glycolipids

73 tinal extract, 90 micrograms/ml heparin, 10% fetal bovine serum, and 10% monkey serum.

74 mination of H2S spiked in whole human blood, fetal bovine serum, and E. coli.

75 g 1% antibiotic/antimycotic solution and 10% fetal bovine serum, and incubated for 24 hours.

76 e perform analyses of human urine and sweat, fetal bovine serum, and rat plasma with their spike anal

77 three complex nutrient sources (neopeptone, fetal bovine serum, and RPMI cell culture medium).

78 tide compositions from 18 glycoproteins from fetal bovine serum, and the glycan structures for most o

79 induced by treating cells for 20 h with 10% fetal bovine serum ( approximately 3 x basal).

80 dose-dependent manner 36 h after addition of fetal bovine serum as a cell growth stimulator.

81 us virus-like particles (VLPs) spiked in 10% fetal bovine serum as a model system, we observed a limi

82 hen incubated for 24h in the presence of 10% fetal bovine serum at 37 degree C, although it is hydrol

83 This hematopoietic differentiation requires fetal bovine serum, but no other exogenous cytokines.

84 Vitronectin was removed from fetal bovine serum by heparin-agarose affinity chromatog

85 ase enrichment with charcoal dextran-treated fetal bovine serum, CD-FBS, as an effective hormone with

86 edium/Ham's F-12 (3:1) supplemented with 10% fetal bovine serum (cDMEM).

87 were cultured in DMEM supplemented with 10% fetal bovine serum, cell populations arose that showed r

88 s adherent to fibrinogen-, immunoglobin-, or fetal bovine serum-coated polystyrene surfaces for 6 hou

89 The identity of the cell adhesive factors in fetal bovine serum, commonly used to supplement growth m

90 t tumor necrosis factor-alpha (TNF-alpha) in fetal bovine serum-containing and serum-free media and w

91 Dulbecco's modified Eagle's medium plus 10% fetal bovine serum (DF) before they were seeded in 3D Ma

92 humor (DMEM-AH), heat-denatured DMEM-AH, 10% fetal bovine serum (DMEM-FBS, the standard culture suppl

93 selenite (ITS) supplement (DMEM/ITS) or 10% fetal bovine serum (DMEM/10% FBS), or in a defined kerat

94 In the presence of fetal bovine serum, endotoxin elevated intracellular Ca2

95 e that carry-over of media supplemented with fetal bovine serum enhances the production of reactive o

96 at 37 degrees C in medium supplemented with fetal bovine serum, epidermal growth factor, fibroblast

97 or Staphylococcus aureus and other proteins (fetal bovine serum, Erythrina cristagalli lectin).

98 Nontransfected R- cells cultured with 10% fetal bovine serum failed to form colonies after 3 weeks

99 Acetylcholinesterase isolated from fetal bovine serum (FBS AChE) was previously characteriz

100 medium (AM) was alleviated in AM without 10% fetal bovine serum (FBS) [AM(-S)].

101 stereomeric adducts of Electric eel (Ee) and fetal bovine serum (FBS) acetylcholinesterase (AChE) ina

102 interest, epidermal growth factor (EGF) and fetal bovine serum (FBS) also increased Src activity in

103 or 2, 6, and 9 days in media containing 0.1% fetal bovine serum (FBS) and 1 of 5 concentrations of PD

104 wal of ES cells cultured in media containing fetal bovine serum (FBS) and a glycogen synthase kinase-

105 ltaneously and without cross-talk in buffer, fetal bovine serum (FBS) and whole blood samples, the la

106 c proteins (EfCP) as a native repertoire and fetal bovine serum (FBS) as a non-native reference.

107 using polycarbonate membrane inserts and 20% fetal bovine serum (FBS) as chemoattractant.

108 from P3 and P10 mice in media containing 2% fetal bovine serum (FBS) but not those from P30 mice, wh

109 l sulfoxide (DMSO) in presence or absence of fetal bovine serum (FBS) can provide reliable cryopreser

110 me periods up to 12 days in media containing fetal bovine serum (FBS) concentrations (0, 0.1, 1, 5, 1

111 density and culture conditions, specifically fetal bovine serum (FBS) concentrations, correlate posit

112 at the TROY/RKIP interaction was enhanced by fetal bovine serum (FBS) exposure, and TROY knockdown al

113 as localized in the nucleus, and exposure to fetal bovine serum (FBS) further increased the amount of

114 Specifically, we explored the impact of fetal bovine serum (FBS) gradients on the behaviour of C

115 Fetal bovine serum (FBS) has been used in eukaryotic cel

116 d to be uniquely sensitive to a component in fetal bovine serum (FBS) identified as serum albumin.

117 In addition, we have shown that fetal bovine serum (FBS) induces Yes auto-phosphorylatio

118 Fetal bovine serum (FBS) is an undefined additive that i

119 e incubated for 1, 3, 6, and 10 days in 0.2% fetal bovine serum (FBS) media containing different conc

120 uctural identification and quantification of fetal bovine serum (FBS) N-linked sialylglycan isomers,

121 microM forskolin in the media containing 1% fetal bovine serum (FBS) on the 4 DIV, surface galC coul

122 cco's modified Eagle's medium (DMEM) plus 2% fetal bovine serum (FBS) or 2% FBS plus EMD (100 microg/

123 ues rely on chemically undefined media using fetal bovine serum (FBS) or chemically defined media uti

124 Fetal bovine serum (FBS) plays a pivotal role in animal

125 72, 84, and 96 hours in medium containing 8% fetal bovine serum (FBS) plus additional growth factors.

126 Mueller Hinton agar (MHA) supplemented with fetal bovine serum (FBS) plus NAD yielded optimal AvP gr

127 Treatment of serum-starved ME-180 cells with fetal bovine serum (FBS) resulted in a rapid increase in

128 Cells incubated with 10% fetal bovine serum (FBS) served as positive controls.

129 pically, this cell line is cultured with 10% Fetal Bovine Serum (FBS) supplement.

130 support hybridoma and mammalian cell growth, fetal bovine serum (FBS) supplemented media are still co

131 s on tissue culture treated (TCT) plastic in fetal bovine serum (FBS) supplemented medium.

132 LY when S. intermedius PC574 was cultured in fetal bovine serum (FBS) than when it was grown in the s

133 rated the detection of human ferritin in 10% fetal bovine serum (FBS) to mimic a real detection envir

134 cells with progestin antagonized effects of fetal bovine serum (FBS) to stimulate cell proliferation

135 A humoral immune response to fetal bovine serum (FBS) was detected in all animals fol

136 Charcoal-dextran-stripped fetal bovine serum (FBS) was found to be more efficient

137 ome-wide CRISPR screen under lipid-rich (10% Fetal Bovine Serum (FBS)) and lipid-limited (1% FBS) con

138 human bronchoalveolar lavage (BAL) fluid and fetal bovine serum (FBS), (ii) survival in macrophages,

139 incubated for 1, 3, 5, and 7 days using 0.1% fetal bovine serum (FBS), 10% FBS +/- 10 microM SB, or 2

140 This article reports the effects of fetal bovine serum (FBS), a physiologically relevant mix

141 or the effects that media additives, such as fetal bovine serum (FBS), can have on viral binding.

142 In the regular culture condition containing fetal bovine serum (FBS), Cdc25C protein levels were sim

143 in three different growth media: DMEM + 10% fetal bovine serum (FBS), DMEM + 10% human platelet lysa

144 m components, as discovered during growth in fetal bovine serum (FBS), elicit a robust increase in th

145 Fetal bovine serum (FBS), fibronectin (Fn), the extracel

146 -12, Dulbecco's modified Eagle's medium, 10% fetal bovine serum (FBS), then for an additional 3-10 da

147 protocol, using media supplemented with 10% fetal bovine serum (FBS), to media supplemented with 2%

148 3% +/- 14% (P < 0.001) in the presence of 5% fetal bovine serum (FBS), whereas XMP.Z enhanced BRP gro

149 earch examined the effects of humic acid and fetal bovine serum (FBS), which are ubiquitous in aquati

150 e presence of cell culture medium containing fetal bovine serum (FBS), which forms a protein corona o

151 serum albumin (BSA) is a major component of fetal bovine serum (FBS), which is commonly used as a cu

152 e demonstrate that deletion of Mcl-1 reduces fetal bovine serum (FBS)-, VEGF-, and IL-6-induced proli

153 cAMP blocked the fetal bovine serum (FBS)-induced degradation of p27(KIP1

154 investigated the putative role of [Ca2+]i in fetal bovine serum (FBS)-stimulated LC20 phosphorylation

155 , bFGF/heparin sulfate (HS)-, TGF-beta1-, or fetal bovine serum (FBS)-supplemented DMEM/F12 medium.

156 -trisphosphate pathway in the presence of 2% fetal bovine serum (FBS).

157 in a Dulbecco's Modified Eagle's Medium with fetal bovine serum (FBS).

158 days in media containing either 0.1% or 10% fetal bovine serum (FBS).

159 using BMSCs expanded ex vivo in medium with fetal bovine serum (FBS).

160 ether grown in the absence or presence of 1% fetal bovine serum (FBS).

161 fied Eagle's medium (DMEM), with and without fetal bovine serum (FBS).

162 and maintained in RPMI media containing 10% fetal bovine serum (FBS).

163 plastic surface, in medium with and without fetal bovine serum (FBS).

164 l conditions, including the concentration of fetal bovine serum (FBS).

165 statistically comparable to 10% and even 20% fetal bovine serum (FBS).

166 .85, MAE = 4.97 mg/dL) in complex media like Fetal Bovine Serum (FBS).

167 o not change in size upon incubation in pure fetal bovine serum (FBS).

168 entiated for 5 or 16 days in the presence of fetal bovine serum (FBS).

169 rate measurement of the G6P concentration in fetal bovine serum (FBS).

170 inhibitor methylisobutylxanthine (IBMX) and fetal bovine serum (FBS).

171 ol diminished the Ca(2+) response induced by fetal bovine serum (FBS).

172 12 nutrient mixture (F-12) in the absence of fetal bovine serum (FBS); this represents a breakthrough

173 v) KnockOut Serum Replacement (SR); 3% (v/v) fetal bovine serum (FBS)] and addition of specific embry

174 d in a normal (N) or defined (D) medium (+/- fetal bovine serum, FBS) under normoxic (N, p(O(2)) = 20

175 scles, and after 3 days in growth media (20% fetal bovine serum, FBS), myoblasts from IUGR fetuses ha

176 Addition of fetal bovine serum, fibroblast growth factor-2 (FGF-2),

177 ore pronounced in cultured cells deprived of fetal bovine serum for 24 h, suggesting that it may be c

178 cultured meat production, such as the use of fetal bovine serum for medium supplementation.

179 l essential medium (alphaMEM) containing 10% fetal bovine serum formed multicellular aggregates withi

180 d in media containing human serum (group 1), fetal bovine serum (group 2), StemPro medium (group 3),

181 ingomyelinase (Zn-SMase) originally found in fetal bovine serum, has received little attention since

182 ells are expanded in media supplemented with fetal bovine serum, horse serum, PIXY321, flt-3 ligand,

183 ol-block-lactide) (mPEG-LA) were unstable in fetal bovine serum, human serum and synovial fluid, with

184 The destabilizing factor in fetal bovine serum, identified as albumin, does not inte

185 However, treatment with 10% fetal bovine serum improved normal chondrocyte survival

186 es as substitutes for critical components of fetal bovine serum in cultured meat production.

187 cretion but was dependent on the presence of fetal bovine serum in the culture media.

188 The presence of 0.2% fetal bovine serum in the culture medium was necessary f

189 appeared to be related to ligands present in fetal bovine serum in the medium.

190 co's minimum essential medium containing 20% fetal bovine serum in the presence of mitomycin C-treate

191 n Dulbecco's minimum essential media and 20% fetal bovine serum in the presence of mitomycin-treated

192 3A2-150] dissolution in physiological media (fetal bovine serum) increases the TT by approximately 2.

193 Whereas fetal bovine serum-induced Akt activation is reconstitut

194 signaling molecules, we found that S1P- and fetal bovine serum-induced CTGF/CCN2 expression were dep

195 ctor-beta1-induced fibroblast activation and fetal bovine serum-induced fibroblast proliferation.

196 thylxanthine (MIX), dexamethasone (DEX), and fetal bovine serum induces a rapid but transient activat

197 confluence in RPMI 1640 supplemented with 5% fetal bovine serum, L-glutamine, and nonessential amino

198 Treatment of HeLa cells with fetal bovine serum markedly increased the phosphothreoni

199 JB6 Cl41 cells were starved in 0.1% fetal bovine serum/MEM for 72 h and then treated with 50

200 ts were treated with the culture supplements fetal bovine serum, N2, and G5 and a mixture of G5 and N

201 ble culture conditions (such as inclusion of fetal bovine serum), necessitating the development of me

202 Explants were grown in RPMI 1640 with 10% fetal bovine serum on coverslips for 8 days or assayed f

203 days in the presence of 25 ng EGF/mL and 10% fetal bovine serum on type I collagen gels, they formed

204 Eliciting biofilm formation required coating fetal bovine serum onto the poly(ether sulfone) microdia

205 ld increase, whereas stimulation with either fetal bovine serum or anisomycin induced an even stronge

206 Interestingly, treatment with fetal bovine serum or exogenous expression of cellular o

207 after serum withdrawal and stimulation with fetal bovine serum or ligands of select receptor tyrosin

208 y inhibited KLF5 induction by LPA but not by fetal bovine serum or phorbol 12-myristate 13-acetate.

209 f rat tracheal smooth muscle stimulated with fetal bovine serum or platelet-derived growth factor, wi

210 significantly increased upon the addition of fetal bovine serum or the phorbol ester, PMA.

211 were treated daily with medium containing 5% fetal bovine serum or the same medium supplemented with

212 diated delivery in the medium with up to 38% fetal bovine serum, outclassing two traditional membrane

213 and NLF cells grown in medium containing 10% fetal bovine serum (P < 0.01).

214 Alternatively, stimulation of the cells by fetal bovine serum produced a reduced response, indicati

215 ation with either epidermal growth factor or fetal bovine serum results in an unexpected rapid and su

216 ucted (i) spike analyses of biomolecule-rich fetal bovine serum sample, confirming that the analytica

217 ied to the H2O2 detection in the disinfected fetal bovine serum samples, and the recovery was obtaine

218 of the cells from complex mixtures including fetal bovine serum samples.

219 essential media, alpha modification with 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-pol

220 However, the matrix (e.g., fetal bovine serum) showed an impact on the retention be

221 A soluble form of the enzyme, isolated from fetal bovine serum, showed the same subunit structure.

222 ent medium containing DEX, MIX, insulin, and fetal bovine serum shows that the beta/delta39 cells exp

223 ITS (serum-free media; SFM) or (B) CMRL +10% fetal bovine serum (standard media) and compared with cr

224 ditionally, canstatin potently inhibited 10% fetal bovine serum-stimulated endothelial cell prolifera

225 Here, RFX1 overexpression reduced fetal bovine serum-stimulated proliferation of SH-SY5Y c

226 Fetal bovine serum strongly impacted the discriminatory

227 ells labeled with [(3)H]cholesterol with 10% fetal bovine serum, suggesting that late endosomes/lysos

228 cells also were hypersensitive to human and fetal bovine serum, suggesting that targeting Ole1 could

229 did not induce cell death in the presence of fetal bovine serum, suggesting that they induce cell dea

230 rolonged islet culture and its comparison to fetal bovine serum-supplemented media and to cryopreserv

231 have a greater rate of proliferation in 10% fetal bovine serum than primary culture, and continued t

232 Several factors, including the presence of fetal bovine serum, the configuration of the tissue cult

233 eks [10 weeks, 2 days]) were cultured in 10% fetal bovine serum, the mean number (+/- SEM) of adheren

234 he G0/G1 phase, i.e., 18 h after addition of fetal bovine serum, the percentages of cells in G0/G1 ph

235 atocyte phenotype, or in DMEM containing 10% fetal bovine serum, to cause the keratocytes to become f

236 d in medium supplemented with Chelex-treated fetal bovine serum, to remove metal ions, levels of ZnT1

237 as not altered by the presence or absence of fetal bovine serum, vascular endothelial growth factor,

238 Proliferation in response to 10% fetal bovine serum was assessed by [3H]thymidine incorpo

239 tion by epidermal growth factor, insulin, or fetal bovine serum was similar to that observed in wild-

240 The levels of S1P and DHS1P in fetal bovine serum were 141.7+/-4.6 and 0.6+/-0.2 pmol/m

241 growing in regular medium supplemented with fetal bovine serum were just as sensitive to loss of ext

242 f trophozoites in dialyzed medium containing fetal bovine serum (which is low in cholesterol) reduced

243 Fetal bovine serum, which can elicit an immune reaction

244 ors, particularly the combination present in fetal bovine serum, which fully suppressed the expressio

245 a multicycle time course in the presence of fetal bovine serum, which inhibits rotavirus spread.

246 pecific antagonist (CORT-108297) or stripped fetal bovine serum, which lacks nuclear hormones and oth

247 ation of macrophages from human monocytes in fetal bovine serum with macrophage-colony-stimulating fa

248 nths in the basal medium (DMEM containing 2% fetal bovine serum) with one medium change per week.

249 ve when cultured in the presence of 10% FBS (fetal bovine serum), with a replication time of 1-3 week

250 proliferation when cells were cultured in 1% fetal bovine serum without added IGF-I.

251 ing translation, preserving the viability of fetal bovine serum without refrigeration, enhancing the