ライフサイエンスコーパス: bovine serum

1 omplex media (bovine serum albumin and fetal bovine serum).

2 nor fraction of EDA2 was also found in fetal bovine serum.

3 and is identical in aqueous buffer and fetal bovine serum.

4 fail to proliferate in the absence of fetal bovine serum.

5 as mouse-derived 3T3 feeder cells and fetal bovine serum.

6 300 pM and 100 nM, in buffer and in diluted bovine serum.

7 ingle OmpG nanopore in the presence of fetal bovine serum.

8 solutions of deionized water and 100% fetal bovine serum.

9 ith absorption and emission >700 nm in fetal bovine serum.

10 biose is exacerbated by the removal of fetal bovine serum.

11 cell culture systems supplemented with fetal bovine serum.

12 effectively detect the exosomes in 30% fetal bovine serum.

13 on the measured charge-state distribution of bovine serum albumin (66.5 kDa), indicating that ion-ion

14 ery of near-infrared fluorescent dye-labeled bovine serum albumin (800CW-BSA, used as a model agent).

15 modification using electrospun amyloid like-bovine serum albumin (AL-BSA) nanofibers on QCM surfaces

16 To address this clinical need, gold cluster bovine serum albumin (AuNC@BSA) nanogates were engineere

17 rated by conjugation of azide functionalized bovine serum albumin (azido-BSA) with azido-fluorescein

18 For bovine serum albumin (BSA) ( approximately 67 kDa), with

19 Bovine serum albumin (BSA) adsorption was studied at dif

20 how much superior fouling resistance against bovine serum albumin (BSA) adsorption, E. coli adhesion,

21 Meanwhile, the introduction of bovine serum albumin (BSA) and antibody (Ab) enhanced th

22 proteins including cardiac myoglobin (MYG), bovine serum albumin (BSA) and cardiac troponin T (cTnT)

23 Bovine serum albumin (BSA) and dextran varying in molecu

24 nt surface properties with various proteins (bovine serum albumin (BSA) and different forms of hemogl

25 capacity (PPC) using two different proteins [bovine serum albumin (BSA) and gelatin], molecular weigh

26 ility and biodegradability, albumins such as bovine serum albumin (BSA) and human serum albumin (HSA)

27 gregation behavior of two model proteins- i) bovine serum albumin (BSA) and ii) beta-galactosidase (b

28 her physiologically relevant components like bovine serum albumin (BSA) and lipopolysaccharide.

29 By using Bovine serum albumin (BSA) and lysozyme, the excellent s

30 st were tested in a model system composed of bovine serum albumin (BSA) and methylglyoxal (MGO).

31 The interference effect of troponin T (TnT), bovine serum albumin (BSA) and myoglobin (Myo) in the pe

32 The strategy was tested on digested bovine serum albumin (BSA) and successfully quantified a

33 The shells comprising alternate layers of bovine serum albumin (BSA) and tannic acid (TA) were tes

34 izopus sp.) hydrolyzed iron oxide-associated bovine serum albumin (BSA) and the factors that affected

35 PTL approach with a 4-plex labeled sample of bovine serum albumin (BSA) and yeast lysates mixed at di

36 9, 1.25 mug/mL) after passive adsorption and bovine serum albumin (BSA) as a blocking agent generated

37 st, the detection method was optimized using Bovine serum albumin (BSA) as a model protein to mimic t

38 ysines of its binding partner SpA but not to bovine serum albumin (BSA) as a nonbinding control.

39 IR)-emitting gold nanoclusters (AuNCs) using bovine serum albumin (BSA) as a protecting agent.

40 e pi (hGSTP), human serum albumin (HSA), and bovine serum albumin (BSA) as model target proteins.

41 were tested for the sensing of biomolecules (bovine serum albumin (BSA) as reference) binding to gate

42 linkages of insulin, alpha-lactalbumin, and bovine serum albumin (BSA) as well as the free C34-BSA w

43 vestigated the interaction of CA and MC with bovine serum albumin (BSA) at pH 3.5, 5.0, and 7.4 using

44 recorded simultaneously during adsorption of bovine serum albumin (BSA) at the surface of the K(+)-IS

45 the quinazolinone core allowed reduction of bovine serum albumin (BSA) binding (63c, 63d).

46 iffness of protein-based hydrogels made from bovine serum albumin (BSA) by using polyelectrolytes suc

47 The variables of interest, such as bovine serum albumin (BSA) concentration, incubation tim

48 del protein Fluorescein isothiocynate (FITC) Bovine Serum Albumin (BSA) conjugate incorporated in the

49 SERS data were collected from a solution of bovine serum albumin (BSA) digested by trypsin as an enz

50 m and treated with palmitate (50 mumol/L) or bovine serum albumin (BSA) for 24 hr.

51 (C12E8) and dodecyl maltoside (DDM) protect bovine serum albumin (BSA) from unfolding in SDS.

52 The results of HS-SPME/GC indicated that bovine serum albumin (BSA) had the highest affinity towa

53 t time, the mechanism of SA interaction with bovine serum albumin (BSA) has been investigated by mult

54 entrapment and in vitro release behaviour of bovine serum albumin (BSA) in chitosan-tripolyphosphate

55 solution, as well as their association with bovine serum albumin (BSA) in phosphate buffer solution

56 Traut's Reagent (TR) was used to thiolate Bovine serum albumin (BSA) in solution followed by chemi

57 cao (Theobroma cacao, L.) seeds and added to bovine serum albumin (BSA) individually and combined as

58 alize the migration of fluorescently labeled bovine serum albumin (BSA) into the nanoslits; and fluor

59 Bovine serum albumin (BSA) is a major component of fetal

60 ence for considerable stabilization of doped bovine serum albumin (BSA) molecules upon adsorption on

61 lex labeling of a yeast proteome spiked with bovine serum albumin (BSA) over a 10-fold dynamic range.

62 de (PVDF) ultrafiltration (UF) membranes and bovine serum albumin (BSA) over a range of ionic strengt

63 scent detection of acetylcholine (ACh) using bovine serum albumin (BSA) protected atomically precise

64 ure-dependent adsorption and denaturation of bovine serum albumin (BSA) protein onto a silica-coated

65 gher adsorption of Concanavalin A (ConA) and Bovine Serum Albumin (BSA) proteins when compared with t

66 ANS complexation by cyclodextrins or bovine serum albumin (BSA) results in a nonhomogeneous s

67 d efficient way; LC-MS of a trypsin-digested bovine serum albumin (BSA) sample provided narrow peaks,

68 A biocompatible nanocomposite including bovine serum albumin (BSA) template Cu nanoclusters (CuN

69 It is demonstrated that the adsorption of bovine serum albumin (BSA) to aqueous gold colloids can

70 We illustrate a method that uses bovine serum albumin (BSA) to control the receptor-acces

71 cture play important roles in the ability of bovine serum albumin (BSA) to form stable nanostructures

72 MDs) and graphite in water by using protein, bovine serum albumin (BSA) to produce single-layer nanos

73 ll kept even when the molar ratio of IgG and bovine serum albumin (BSA) tryptic digest mixtures reach

74 As a case study, we choose to monitor bovine serum albumin (BSA) unspecific adsorption, which

75 gate the interaction between glutathione and bovine serum albumin (BSA) using ultraviolet-visible (UV

76 determining the heat denaturation degree of bovine serum albumin (BSA) was assessed.

77 By culture media modifications, bovine serum albumin (BSA) was identified as blocking in

78 In this system, bovine serum albumin (BSA) was immobilized on gold grids

79 yanidin-3-glucoside (CYG) through binding to bovine serum albumin (BSA) was investigated at pH 3.0 us

80 Moreover, the adsorption of bovine serum albumin (BSA) was significantly reduced at

81 The interaction between Allura Red and bovine serum albumin (BSA) was studied in vitro at pH 7.

82 ) were immobilized via EDC-NHS chemistry and Bovine serum albumin (BSA) was used for blocking of the

83 The third electrode covered with Bovine Serum Albumin (BSA) was used for the control of n

84 was coated onto polystyrene well plates and bovine serum albumin (BSA) was used to block unsaturated

85 e ester (GMBS), NeutrAvidin, anti-gp120, and bovine serum albumin (BSA) were also quantified by the P

86 beta-Lg), alpha-lactalbumin (alpha-Lac), and bovine serum albumin (BSA) were bound to beta-C with ove

87 ation of patients, antibodies against native bovine serum albumin (BSA) were detected.

88 adsorption followed by a post-treatment with bovine serum albumin (BSA) which served as the blocking

89 this study, we evaluated the interaction of bovine serum albumin (BSA) with AP and AS using surface

90 In this report, a stepwise unfolding of bovine serum albumin (BSA) with guanidine hydrochloride

91 monstrated by carrying out the hydrolysis of bovine serum albumin (BSA) within 1h, and the assay was

92 ted that a protein (cytochrome c (Cytc c) or bovine serum albumin (BSA)) can be employed to gate fluo

93 g. cytochrome C (Cyt-C), myoglobin (MYO) and bovine serum albumin (BSA)) have been used to evaluate t

94 ns (Trypsin Inhibitor (TI); Ovalbumin (OVA); Bovine Serum Albumin (BSA)), we observe resolution of th

95 and isomeric glycated peptides (fragments of bovine serum albumin (BSA)).

96 pitcher-plant leaves at different rates with bovine serum albumin (BSA), a molecular substitute for d

97 Compared to Y-tube compartments with bovine serum albumin (BSA), GDNF and NGF increased the m

98 After conjugation to bovine serum albumin (BSA), glycoconjugates 1 to 6 were

99 (2+) complex with a model transport protein, bovine serum albumin (BSA), have been explored by means

100 ith heat-inactivated CPE, antibody alone, or bovine serum albumin (BSA), indicating that increased os

101 research on albumin hydrogels has focused on bovine serum albumin (BSA), leaving human serum albumin

102 eting proteins including chymotrypsin (chy), bovine serum albumin (BSA), lysozyme (lyz) and cytochrom

103 to NaCl solutions), unspecific adsorption of bovine serum albumin (BSA), or specific lectin binding o

104 r both deposited gold film and adsorption of bovine serum albumin (BSA), respectively, on poly(methyl

105 samples, with or without spiked additions of Bovine Serum Albumin (BSA), showed considerable disagree

106 peptide-organophosphate hydrolase (ELP-OPH), bovine serum albumin (BSA), titanium dioxide nanofibers

107 anoflow HPLC separations; tryptic digests of bovine serum albumin (BSA), transferrin factor (TF), and

108 five proteins (myoglobin, troponin C, actin, bovine serum albumin (BSA), tropomyosin) were deposited

109 kidney (NRK) cells and SWNTs dispersed with bovine serum albumin (BSA), we demonstrate that the meth

110 Bovine serum albumin (BSA), whey protein isolate (WPI),

111 ion, giving improved performance relative to bovine serum albumin (BSA)-blocked paper.

112 lass in a simulated biothreat scenario using bovine serum albumin (BSA).

113 s) were prepared from inherent biocompatible bovine serum albumin (BSA).

114 bumin (HSA), fatty acid free HSA (ffHSA) and bovine serum albumin (BSA).

115 ng of purified proanthocyanidin oligomers to bovine serum albumin (BSA).

116 temperature (T(d)) and heat-set gelation of bovine serum albumin (BSA).

117 (R(2) = 0.825) with tannin precipitation by bovine serum albumin (BSA).

118 ty towards breast cancer antigen CA-15.3 and bovine serum albumin (BSA).

119 e dependence in detail for the model protein bovine serum albumin (BSA).

120 oglobulin (BLG), alpha-lactalbumin (ALA) and bovine serum albumin (BSA).

121 (FITC) was conjugated to the amino groups of bovine serum albumin (BSA).

122 ng serum or serum-derived components such as bovine serum albumin (BSA).

123 en holes in the bilayer were backfilled with bovine serum albumin (BSA).

124 adical polymerization from the model protein bovine serum albumin (BSA).

125 Bovine serum albumin (BSA)/curcumin binding and dye phot

126 ower, FRAP) and anti-glycation activity by a bovine serum albumin (BSA)/fructose model system were an

127 ssay (FRAP) and anti-glycation activity by a bovine serum albumin (BSA)/fructose model system.

128 Using bovine serum albumin (BSA)/galactose or BSA/glucose as e

129 ve activity of extracts was evaluated in the bovine serum albumin (BSA)/glucose system.

130 s indicated that 16 nm AuNPs stabilized with bovine serum albumin (BSA-cit-AuNPs) was slightly more s

131 eptides from a simulated tryptic digest with bovine serum albumin (BSA:casein, 100:1).

132 loped the biomimetic nanoparticles (cationic bovine serum albumin (CBSA) conjugated siS100A4 and exos

133 lification strategy based on carbon nanotube-bovine serum albumin (CNT-BSA) hybrid system, by which s

134 esented as densely immobilized conjugates of bovine serum albumin (DNP-BSA) or mobile in a supported

135 MN, with free E2 and with E2 conjugated with bovine serum albumin (E2 BSA), alone or in sequence, by

136 We encapsulated fluorescent-bovine serum albumin (FITC-BSA) inside the gel.

137 e dye and fluorescein isothiocyanate-labeled bovine serum albumin (FITC-BSA).

138 A simple post-adsorption of human serum:bovine serum albumin (HS:BSA) mixtures onto the folic ac

139 Methylated-bovine serum albumin (mBSA), but not vehicle challenge,

140 NASH, mice were immunized with MDA-adducted bovine serum albumin (MDA-BSA) before feeding the MCD di

141 3 kDa); however, ion mobility resolution for bovine serum albumin (MW ~ 68 kDa) is less than ~20, whi

142 ss molecularly imprinted polymer coated with bovine serum albumin (RAMIP-BSA) was synthesized, charac

143 ell death was evaluated, and FITC conjugated bovine serum albumin across monolayer hRECs served as an

144 .0% (v/v) caproic acid (a lipid), 0.1% (w/v) bovine serum albumin and 0.01% (w/v) cytochrome C (both

145 between energy flow through the structure of bovine serum albumin and allosteric interactions between

146 o validate the method, two protein isolates; bovine serum albumin and casein were investigated for th

147 uantum clusters (AuQC@BSA) synthesized using bovine serum albumin and conjugated with acetylcholinest

148 ized to demonstrate protein binding by using bovine serum albumin and detection of antibody-antigen i

149 ) in physiologically relevant complex media (bovine serum albumin and fetal bovine serum).

150 Bovine serum albumin and gamma-Globulin were chosen as m

151 examine the morphology of hydrogels made of bovine serum albumin and gelatin following high pressure

152 s, as demonstrated for tryptic peptides from bovine serum albumin and Halobacterium salinarum in a hi

153 ignificant levels of non-specific binding of bovine serum albumin and human serum albumin.

154 binding and uptake of Alexa488-fluorophore, bovine serum albumin and quantum dot cargoes.

155 LMG-bovine serum albumin and rabbit anti-sheep IgG were immo

156 ion of the pressure effect was performed for bovine serum albumin and thyroglobulin that required gra

157 onstrated via the covalent immobilization of bovine serum albumin antibody (anti-BSA) and fibrinogen

158 When measuring a bovine serum albumin aqueous solution, the limit of dete

159 Chitosan capped gold nanoparticles on bovine serum albumin are proposed as an ultrasensitive p

160 Furthermore, using bovine serum albumin as a model protein, the trivalent o

161 Using sulforhodamine b, zidovudine, and bovine serum albumin as model hydrophilic drugs, we foun

162 That was similarly observed for bovine serum albumin at a subcritical water temperature

163 We initiate this effort by considering bovine serum albumin because it is a globular protein wh

164 ifically employ the LN-IMS system to examine bovine serum albumin binding to gold nanoparticles.

165 t relied on the quantitation of extravasated bovine serum albumin conjugated to Evans Blue, as an ind

166 orescent proteins and stochastically labeled bovine serum albumin containing up to 24 fluorophores.

167 ecoveries of the enrichment step from spiked bovine serum albumin digests were >80% for the commercia

168 s of cytochrome c, ubiquitin, myoglobin, and bovine serum albumin formed by electrospray ionization a

169 ects of Centella asiatica phenolics (CAP) on bovine serum albumin glycoxidation in a BSA-glucose mode

170 lucose syrup on the structural properties of bovine serum albumin has been addressed in preparations

171 ured on a test line comprised of the protein bovine serum albumin immobilized on nitrocellulose.

172 The control experimentation using 5mg/mL bovine serum albumin in PBS and nonspecific surface test

173 s of cortisol solutions in a complex matrix (bovine serum albumin in phosphate buffered saline) is al

174 a detection limit of ~110 fg/mL biotinylated bovine serum albumin in serum.

175 retreatment of the particle supernatant with bovine serum albumin mitigates the negative effects of f

176 y and used for recording the binding between Bovine Serum Albumin molecules immobilized onto the surf

177 ue unaltered when the assay was processed in bovine serum albumin or human serum.

178 A bovine serum albumin pretreatment protocol was developed

179 was determined that an in-line injection of bovine serum albumin prior to analyte injection yielded

180 nal approaches, allowing us to detect single bovine serum albumin proteins with a molecular weight of

181 The plasmonic construct consists of a bovine serum albumin scaffold with approximately 210 IRD

182 e validated using IDA in intact and digested bovine serum albumin solutions using the TCN (98 and 100

183 t be duplicated by the use of hyaluronate or bovine serum albumin solutions.

184 ee-dimensional porous matrix of cross-linked bovine serum albumin supported by a network of conductiv

185 or 15min at ambient temperature on condensed bovine serum albumin systems (BSA) with up to 80% w/w so

186 osity measurements clearly indicate that the bovine serum albumin tertiary structure changes as prote

187 ns of both mixtures of small molecules and a bovine serum albumin tryptic digest, TASF improved the p

188 Avidin detection was not perturbed by Bovine Serum Albumin up to 50,000 mug mL(-1).

189 o detect miRNA-21 in human serum albumin and bovine serum albumin was almost identical to that in PBS

190 Bovine serum albumin was also tested as a protein standa

191 The captured molecular BPA-bovine serum albumin was covalently immobilized on the s

192 timate total chemical delivery time, labeled bovine serum albumin was injected in the channel chamber

193 Using this method, a model protein bovine serum albumin was investigated over 3 days of inc

194 isotopic pattern of multiply charged ions of bovine serum albumin was obtained with 1.5 s transients.

195 that forms upon exposure of nanoparticles to bovine serum albumin was utilized as a nanoparticle stab

196 ples, mid-IR spectra of Escherichia coli and bovine serum albumin were recorded.

197 Only penetratin showed effective uptake of bovine serum albumin with the phenylalanine variant show

198 of the minor (lactoferrin, lactoperoxidase, bovine serum albumin) and major (alpha-lactalbumin, beta

199 od clearance of (13)C-PEG and PEGylated-BSA (bovine serum albumin) following their intravenous inject

200 of a NIST Standard Reference Material 927e (bovine serum albumin), a high-purity immunoglobulin G 1k

201 omically precise gold clusters, Au@BSA (BSA, bovine serum albumin), coated on Nylon-6 nanofibers were

202 ng compounds (sucrose, dopamine, starch, and bovine serum albumin), resulting in negligible cross-rea

203 Only Ag-NPs functionalized with BSA (bovine serum albumin), which is a protein with the funct

204 gg yolk and positive co-protein effects with bovine serum albumin, (S-)ovalbumin, egg white, whole eg

205 Da) synthetic dimer between cytochrome c and bovine serum albumin, a 30% yield of the purified, isola

206 ee different substrates: collagen-I (Col-I), bovine serum albumin, and a monolayer of bone marrow-der

207 tides from three model proteins, hemoglobin, bovine serum albumin, and beta-casein, and compare the r

208 e also encapsulate a model globular protein, bovine serum albumin, and calculate its loading efficien

209 ysozyme, cytochrome c, myoglobin, ovalbumin, bovine serum albumin, and etanercept were investigated.

210 hree proteins, alphaB-crystalline (alphaBc), bovine serum albumin, and hen egg-white lysozyme (HEWL)

211 polypropylene glycol (PPG), angiotensin II, bovine serum albumin, and the "thermometer" compound p-m

212 ting a mixture of microcystins to cationised bovine serum albumin, and the plate-coating antigen was

213 the extent of supercharging was probed using bovine serum albumin, beta-lactoglobulin, and lysozyme,

214 pha, ovalbumin, human transthyretin, avidin, bovine serum albumin, concanavalin, human serum amyloid

215 sor with four reference molecules (dopamine, bovine serum albumin, glucose and elongated peptide) was

216 Moreover, a protein mixture containing bovine serum albumin, GST, and ubiquitin could be specif

217 nitoring the glycation process in samples of bovine serum albumin, human serum albumin, and lysozyme.

218 Bovine serum albumin, lactoferrin, and alpha-casein (S1

219 ther proteins, such as transferrin, heparin, bovine serum albumin, mucin, or collagen IV.

220 einase 8 (MMP-8), minocycline hydrochloride, bovine serum albumin, or an antibacterial peptide (KSL)

221 ructed by sequential immobilization of UPEC, bovine serum albumin, primary antibody and Horse Radish

222 verage for both trypsin and Lys C digests of bovine serum albumin, providing ECD spectra for doubly c

223 nt amphoteric compounds, such as hemoglobin, bovine serum albumin, R-phycoerythrin, and histidine, wi

224 gh selectivity 1:400 horse radish peroxidase/bovine serum albumin, sensitivity to 100 attomoles, reco

225 moderately affected by beta-cyclodextrin and bovine serum albumin, taken as models of food macromolec

226 ism, but it utilizes coating agents, such as bovine serum albumin, to create consistent rotation and

227 trostatically adsorbed films of the protein, bovine serum albumin, with different alpha-helix and bet

228 tching-induced fluorescence quenching of the bovine serum albumin-protected Au25 nanoclusters (BSAGNC

229 A mass balance model based on bovine serum albumin-water (D(BSA/w)) and liposome-water

230 t analysis of peptides from trypsin digested bovine serum albumin.

231 by E. coli cells and does not interact with bovine serum albumin.

232 phosphine-derivatized fluorophore-conjugated bovine serum albumin.

233 e and in combination of calcium alginate and bovine serum albumin.

234 ependent, and its washout was accelerated by bovine serum albumin.

235 alleviated when SWCNTs were pre-coated with bovine serum albumin.

236 in tails that have been covalently linked to bovine serum albumin.

237 cytochrome c, 90% for myoglobin, and 65% for bovine serum albumin.

238 n the presence of either FLAG octapeptide or bovine serum albumin.

239 orbic acid, dopamine, uric acid, glucose and bovine serum albumin.

240 eins: melittin, cytochrome c, myoglobin, and bovine serum albumin.

241 n poorly defined albumin supplements such as bovine serum albumin.

242 sed with tetraconazole haptens conjugated to bovine serum albumin.

243 tide B spiked in a protein digest mixture of bovine serum albumin.

244 ver nanoparticles in ethanolic solutions and bovine serum albumin.

245 n controlled hydrolysis and precipitation of bovine serum albumin.

246 ed by a cross-linked membrane of amphiphilic bovine serum albumin/poly(N-isopropylacrylamide) (BSA-NH

247 al RI containing small (glycerol) and large (bovine serum albumin; BSA) analyte molecules, indicating

248 itatively by a bichinchonic acid assay using bovine-serum albumin (BSA) as a protein model on the l-c

249 ps in their force curves, while PC3 cells on bovine-serum-albumin- and antibody-treated PC3 cells sho

250 ng selected the affinity interaction between bovine serum albumine (BSA) with anti-BSA antibody (AB)

251 valuated using Escherichia coli bacteria and bovine serum albumine (BSA).

252 critically important to prevent confounding bovine serum amine oxidase-induced cytotoxicity in mecha

253 re quickly oxidized by the copper-containing bovine serum amine oxidase.

254 erein alpha-MEM (supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic) was perfused

255 erein alpha-MEM (supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic) was perfused

256 gets in the presence of complex media (fetal bovine serum) and other interfering DNA fragments in the

257 on of H2S spiked in whole human blood, fetal bovine serum, and E. coli.

258 ntibiotic/antimycotic solution and 10% fetal bovine serum, and incubated for 24 hours.

259 ity toward Cys-SeH in aqueous PBS buffer, in bovine serum, and on the silica gel surface that lead to

260 should be avoided because of the presence of bovine serum, but the tissue can be washed using balance

261 leukocyte chemoattractant was isolated from bovine serum by an established four-step purification pr

262 rs aged in Phosphate Buffered Saline, Foetal Bovine Serum, Dulbecco's - Minimum Essential Medium (wit

263 rcity of bone marrow donors, and reliance on bovine serum during mesenchymal stem/stromal cell prolif

264 sensor was also able to determine zinc in a bovine serum extract, and the results were verified with

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

266 ES cells cultured in media containing fetal bovine serum (FBS) and a glycogen synthase kinase-3 (GSK

267 usly and without cross-talk in buffer, fetal bovine serum (FBS) and whole blood samples, the latter b

268 oxide (DMSO) in presence or absence of fetal bovine serum (FBS) can provide reliable cryopreservation

269 TROY/RKIP interaction was enhanced by fetal bovine serum (FBS) exposure, and TROY knockdown also led

270 Fetal bovine serum (FBS) has been used in eukaryotic cell cult

271 e uniquely sensitive to a component in fetal bovine serum (FBS) identified as serum albumin.

272 In addition, we have shown that fetal bovine serum (FBS) induces Yes auto-phosphorylation and

273 l identification and quantification of fetal bovine serum (FBS) N-linked sialylglycan isomers, during

274 n S. intermedius PC574 was cultured in fetal bovine serum (FBS) than when it was grown in the standar

275 the detection of human ferritin in 10% fetal bovine serum (FBS) to mimic a real detection environment

276 This article reports the effects of fetal bovine serum (FBS), a physiologically relevant mixture o

277 onents, as discovered during growth in fetal bovine serum (FBS), elicit a robust increase in the amou

278 examined the effects of humic acid and fetal bovine serum (FBS), which are ubiquitous in aquatic envi

279 ence of cell culture medium containing fetal bovine serum (FBS), which forms a protein corona on the

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

281 ic surface, in medium with and without fetal bovine serum (FBS).

282 ulbecco's Modified Eagle's Medium with fetal bovine serum (FBS).

283 normal (N) or defined (D) medium (+/- fetal bovine serum, FBS) under normoxic (N, p(O(2)) = 20%) or

284 and after 3 days in growth media (20% fetal bovine serum, FBS), myoblasts from IUGR fetuses had 34%

285 edia containing human serum (group 1), fetal bovine serum (group 2), StemPro medium (group 3), protam

286 ck-lactide) (mPEG-LA) were unstable in fetal bovine serum, human serum and synovial fluid, with varyi

287 The destabilizing factor in fetal bovine serum, identified as albumin, does not interfere

288 oteases relative to antibodies from human or bovine serum, making them of particular interest as oral

289 ing biofilm formation required coating fetal bovine serum onto the poly(ether sulfone) microdialysis

290 pecific adsorption surface coverage of crude bovine serum proteins.

291 (i) spike analyses of biomolecule-rich fetal bovine serum sample, confirming that the analytical reli

292 ies and a good percentage recovery in spiked bovine serum sample.

293 n, with sensitivities of 77%, 45%, and 9% in bovine serum samples from the United Kingdom (n = 126),

294 the H2O2 detection in the disinfected fetal bovine serum samples, and the recovery was obtained abou

295 hozoites in dialyzed medium containing fetal bovine serum (which is low in cholesterol) reduced raft

296 We find that cells cultured in adult bovine serum, which better reflects nutrients available

297 oPAD-Ep for simple separation of proteins in bovine serum, which illustrates its potential applicatio

298 ticycle time course in the presence of fetal bovine serum, which inhibits rotavirus spread.

299 c antagonist (CORT-108297) or stripped fetal bovine serum, which lacks nuclear hormones and other gro

300 n cultured in the presence of 10% FBS (fetal bovine serum), with a replication time of 1-3 weeks.