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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 72, 84, and 96 hours in medium containing 8% fetal bovine serum (FBS) plus additional growth factors.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 -12, Dulbecco's modified Eagle's medium, 10% fetal bovine serum (FBS), then for an additional 3-10 da

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

78 3% +/- 14% (P < 0.001) in the presence of 5% fetal bovine serum (FBS), whereas XMP.Z enhanced BRP gro

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 .85, MAE = 4.97 mg/dL) in complex media like Fetal Bovine Serum (FBS).

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

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

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

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

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

102 12 nutrient mixture (F-12) in the absence of fetal bovine serum (FBS); this represents a breakthrough

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

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

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

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

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

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

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

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

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

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

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

114 Complexation of fetal bovine serum acetylcholinesterase with monoclonal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 Fetal bovine serum strongly impacted the discriminatory

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

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

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

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

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

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

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

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

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

182 3A2-150] dissolution in physiological media (fetal bovine serum) increases the TT by approximately 2.

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

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

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

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

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

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

189 8, or 60 hours in culture medium (M-199, 10% fetal bovine serum, 10 ng/ml epidermal growth factor, 20

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

191 0, 72, and 84 hours to medium containing 10% fetal bovine serum, 20 ng/ml fibroblast growth factor, a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

226 Fetal bovine serum, which can elicit an immune reaction

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

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

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

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

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

232 Whereas fetal bovine serum-induced Akt activation is reconstitut

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

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

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

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

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

238 of epithelial cell culture media containing fetal bovine serum.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

259 alian cell culture systems supplemented with fetal bovine serum.

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

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

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

263 5pg/ml for assays containing PBS spiked with fetal bovine serum.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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