ライフサイエンスコーパス: fetal bovine

1 othioate modification exhibited stability in fetal bovine and human serum.

2 )-doped, silica nanoshells were submerged in fetal bovine and human serums at physiological temperatu

3 Confluent fetal bovine aortic endothelial (FBAE) cells were incuba

4 proteins in the secretory pathway in intact fetal bovine auricular chondrocytes.

5 In non-denaturing extracts of fetal bovine cartilage and in human skin fibroblast cult

6 eration of cartilage extracellular matrix by fetal bovine chondrocytes maintained in pellet culture,

7 oteoglycan decorin in the medium of cultured fetal bovine chondrocytes.

8 stogenic cells, human dermal fibroblasts and fetal bovine chondrocytes.

9 in-1) were prominent in equimolar amounts in fetal bovine epiphyseal cartilage and absent from adult

10 ansgenic embryonic stem (ES)-like cells from fetal bovine fibroblasts.

11 d the activity of TGF-beta1 and TGF-beta2 in fetal bovine heart endothelial (FBHE) cell proliferation

12 Proliferation of fetal bovine heart endothelial (FBHE) cells was inhibite

13 The alpha(2)M* inhibits FGF-2-dependent fetal bovine heart endothelial cell proliferation in a d

14 was demonstrated to adhere to and to invade fetal bovine heart endothelial cells (FBHEC), bovine aor

15 teraction of TGF-beta1 with its receptors in fetal bovine heart endothelial cells.

16 Clear fetal bovine lenses, photolyzed under the identical cond

17 In fetal bovine lung cells but not in a human epithelial ce

18 valuate fibrillin-1 deposition in the ECM of fetal bovine nuchal ligament cells after culture in ADAM

19 When cultured in ADAMTSL4-containing medium, fetal bovine nuchal ligament cells showed accelerated fi

20 role of ADAMTS10 in microfibril biogenesis, fetal bovine nuchal ligament cells were cultured in the

21 Fetal bovine osteoblasts were assessed for osteoblast mi

22 Fetal bovine retinal pigment epithelium (RPE) was grown

23 Fetal bovine secretory and maturation stage enamel sampl

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

45 72, 84, and 96 hours in medium containing 8% fetal bovine serum (FBS) plus additional growth factors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

61 -12, Dulbecco's modified Eagle's medium, 10% fetal bovine serum (FBS), then for an additional 3-10 da

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

63 3% +/- 14% (P < 0.001) in the presence of 5% fetal bovine serum (FBS), whereas XMP.Z enhanced BRP gro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

83 12 nutrient mixture (F-12) in the absence of fetal bovine serum (FBS); this represents a breakthrough

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

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

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

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

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

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

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

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

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

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

94 Complexation of fetal bovine serum acetylcholinesterase with monoclonal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

154 3A2-150] dissolution in physiological media (fetal bovine serum) increases the TT by approximately 2.

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

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

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

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

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

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

161 8, or 60 hours in culture medium (M-199, 10% fetal bovine serum, 10 ng/ml epidermal growth factor, 20

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

163 0, 72, and 84 hours to medium containing 10% fetal bovine serum, 20 ng/ml fibroblast growth factor, a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

192 Fetal bovine serum, which can elicit an immune reaction

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

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

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

196 Whereas fetal bovine serum-induced Akt activation is reconstitut

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

219 5pg/ml for assays containing PBS spiked with fetal bovine serum.

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

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

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

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

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

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

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

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

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

229 of epithelial cell culture media containing fetal bovine serum.

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

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

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

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

234 (PDGFRalpha) positive progenitor cells from fetal bovine skeletal muscle and induced into adipocytes

235 amined in early (95 and 110 gestational day) fetal bovine spleens.

236 Delta helicase isolated from fetal bovine thymus had an apparent M(r) of 115 kDa in S

237 s with DNA polymerase delta (pol delta) from fetal bovine thymus tissue.

238 now purified HS2NF5 to near-homogeneity from fetal bovine thymus.