ライフサイエンスコーパス: bovine serum

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

2 300 pM and 100 nM, in buffer and in diluted bovine serum.

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

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

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

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

7 for assays containing PBS spiked with fetal bovine serum.

8 itioned by AGS cells in the absence of fetal bovine serum.

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

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

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

12 f PNP and XOD cross-linked with a mixture of bovine serum albumen (BSA) and gultaraldehyde (GLA).The

13 own that in the case of trypsin digestion of bovine serum albumen (BSA) more peptides and higher sequ

14 re immunized with 2-octynoic acid coupled to bovine serum albumin (2OA-BSA), leading to the productio

15 rbonic anhydrase (six peptides), and 51% for bovine serum albumin (33 peptides).

16 the epitope peptide was covalently linked to bovine serum albumin (67 kDa) or R-phycoerythrin (240 kD

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

18 binding interactions detection between anti-bovine serum albumin (anti-BSA) and BSA antigen have bee

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

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

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

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

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

24 retention of NPs on glass beads coated with bovine serum albumin (BSA) and alginate were also studie

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

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

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

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

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

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

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

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

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

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

35 gligible interference from troponin T (TnT), bovine serum albumin (BSA) and urea under SWV assays, sh

36 entrenched doctrine that uncritically treats bovine serum albumin (BSA) as a colloidal hard sphere by

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

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

42 igated the binding of several polyphenols to bovine serum albumin (BSA) at pH 7.5 and 25 degrees C: c

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

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

45 eled substrate peptide as it conjugates to a bovine serum albumin (BSA) cosubstrate of larger hydrody

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

47 The bovine serum albumin (BSA) fraction of WPI was found to

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

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

50 eated and assessed on the BS(3)-cross-linked bovine serum albumin (BSA) homodimer.

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

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

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

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

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

56 ilica layer with small pores which prevented bovine serum albumin (BSA) molecules from interacting wi

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

58 d microarrays of fluorophore-labeled IgG and bovine serum albumin (BSA) on FAST, Unisart, and Oncyte-

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

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

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

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

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

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

65 face functionalization of the particles with bovine serum albumin (BSA) showed the ability to capture

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

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

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

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

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

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

72 A) was used to capture HSA specifically, and bovine serum albumin (BSA) was applied to block the non-

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

74 Bovine serum albumin (BSA) was extracted and isolated fr

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

76 a food colourant, quinoline yellow (Qy), and bovine serum albumin (BSA) was investigated by spectroph

77 olid sample AMS (SS-AMS), reduced and native bovine serum albumin (BSA) was modified by (14)C-iodoace

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

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

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

81 Bovine serum albumin (BSA) was used to block non-specifi

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

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

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

85 system generated confident identification of bovine serum albumin (BSA) with 19% sequence coverage an

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

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

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

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

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

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

92 Bovine serum albumin (BSA), a model protein, reduced the

93 our model proteins (cytochrome c, myoglobin, bovine serum albumin (BSA), and beta-casein) was used as

94 is bleached at a low rate in the presence of bovine serum albumin (BSA), and intermediate photoproduc

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

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

97 of various types of proteins represented by bovine serum albumin (BSA), heme-containing myoglobin (M

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

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

100 incubated for 40 min in aqueous solutions of bovine serum albumin (BSA), lysozyme and IgG (5x10(-7) m

101 e demonstrated that coatings of fibronectin, bovine serum albumin (BSA), or collagen with or without

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

103 s(acetylthio) octanoic acid (SAc)-conjugated bovine serum albumin (BSA), recombinant PDC-E2 (rPDC-E2)

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 the absence of analyte protein, in our case bovine serum albumin (BSA), the protein-coated QDs bind

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

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

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

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

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

112 he quantification of proteins was 130 pg for bovine serum albumin (BSA), which is an improvement of n

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

114 erse DWMS were fabricated with model protein bovine serum albumin (BSA)-loaded poly(lactide-co-glycol

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

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

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

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

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

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

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

122 immunosensing electrodes were blocked using bovine serum albumin (BSA).

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

124 amino acids or proteins, such as cysteine or bovine serum albumin (BSA).

125 involving a pH adjustment before addition of bovine serum albumin (BSA).

126 as covalent binding of fluorescently tagged bovine serum albumin (BSA).

127 ecovery of signal from 2.5 nM thrombin in 2% bovine serum albumin (BSA).

128 d peptide mixtures contaminated 50-fold with bovine serum albumin (BSA).

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

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

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

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

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

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

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

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

137 ded solutions with steric cosolutes [40% w/v bovine serum albumin (BSA)], the parallel G-quadruplex c

138 l results for the collection of FITC-labeled bovine serum albumin (BSA, 0.033nM) were as high as near

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

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

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

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

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

144 protein (fluorescein isothiocyanate-labelled bovine serum albumin (FTIC-BSA)) macromolecules.

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

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

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

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

149 propionate acrylate (functional monomer) and bovine serum albumin (template) for polymerization in aq

150 .0% (v/v) caproic acid (a lipid), 0.1% (w/v) bovine serum albumin and 0.01% (w/v) cytochrome C (both

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

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

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

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

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

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

157 two model complex systems (gold nanoparticle-bovine serum albumin and polystyrene bead-antibody) as a

158 onic interactions between negatively charged bovine serum albumin and positively charged imprinted na

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

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

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

162 -like (Dll)1 to induce Notch signaling or to bovine serum albumin as control.

163 oating than when PEO was used, or when using bovine serum albumin as the blocking agent.

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

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

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

167 This approach using bovine serum albumin blocked 11-MUA-Au NDs provided a li

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

169 econcentration profiles of a fluorescein and bovine serum albumin derivatized with this fluorescent t

170 The selectively encapsulated bovine serum albumin first gets reduced at -0.9V and the

171 insult through intraperitoneal injections of bovine serum albumin for 7 days.

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

173 For individual proteins, bovine serum albumin had higher binding affinity with no

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

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

176 practical sensor for ultra-trace analysis of bovine serum albumin in clinical settings.

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

178 uorescence imaging of fluorescein-conjugated bovine serum albumin in the delay line and by demonstrat

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

180 , and ferrocene methanol) in the presence of bovine serum albumin or fibrinogen was studied at macrop

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

182 High concentrations of bovine serum albumin or lysozyme (protein crowders) to m

183 pressing CT26 cells (CT26/mbetaG) but not on bovine serum albumin or non-beta-glucuronidase-expressin

184 ice was mixed in an emulsion stabilised with bovine serum albumin or phospholipids the maximum extrac

185 , up to a dodecasaccharide, as well as their bovine serum albumin or recombinant diphtheria toxin con

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

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

188 dermal growth factor receptor 2 (HER2), in a bovine serum albumin solution using the antibody-modifie

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

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

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

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

193 and its unphosphorylated form, prepared in a bovine serum albumin tryptic digest.

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

195 Bovine serum albumin was also tested as a protein standa

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

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

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

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

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

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

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

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

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

205 hion is made heavier by complexion with BSA (bovine serum albumin), this latter step only required by

206 For BSA (bovine serum albumin), we exhibit that the variation of

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

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

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

210 y-mediated capture of C-reactive protein and bovine serum albumin, along with hybridization of oligon

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

212 analysis of substance P, a tryptic digest of bovine serum albumin, and a phosphopeptide mixture.

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

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

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

216 e composed of tryptic peptides from caseins, bovine serum albumin, and phosphopeptide standards.

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

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

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

220 emically defined model systems consisting of bovine serum albumin, Co(2+), and myristate were studied

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

222 presence of large excess of bovine thrombin, bovine serum albumin, cytochrome C, lysozyme and myoglob

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

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

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

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

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

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

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

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

231 d particles and the other with vacuum-dried, bovine serum albumin-conjugated particles.

232 the cadmium-ethylenediaminetetraacetic acid-bovine serum albumin-gold nanoparticles (Cd-EDTA-BSA-AuN

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

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

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

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

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

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

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

240 sed with tetraconazole haptens conjugated to bovine serum albumin.

241 n the tracer self-diffusion coefficient than Bovine serum albumin.

242 sulfoxide, reducing agents, detergents, and bovine serum albumin.

243 nes were markedly reduced in the presence of bovine serum albumin.

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

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

246 phosphine-derivatized fluorophore-conjugated bovine serum albumin.

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

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

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

250 te kinase (ADK), ribose binding protein, and bovine serum albumin] were characterized.

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

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

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

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 RMPI-1640 medium supplemented with 20% fetal bovine serum and performed a Cell Death ELISA after melp

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

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

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

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

261 us-like particles (VLPs) spiked in 10% fetal bovine serum as a model system, we observed a limit of d

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

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

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

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

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

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

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

269 eins (EfCP) as a native repertoire and fetal bovine serum (FBS) as a non-native reference.

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

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

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

273 issue culture treated (TCT) plastic in fetal bovine serum (FBS) supplemented medium.

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 e regular culture condition containing fetal bovine serum (FBS), Cdc25C protein levels were similar i

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

279 col, using media supplemented with 10% fetal bovine serum (FBS), to media supplemented with 2% HS.

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

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

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

283 change in size upon incubation in pure fetal bovine serum (FBS).

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

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

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

287 0] dissolution in physiological media (fetal bovine serum) increases the TT by approximately 2.2 degr

288 e treated with the culture supplements fetal bovine serum, N2, and G5 and a mixture of G5 and N2 comp

289 pecific adsorption surface coverage of crude bovine serum proteins.

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

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

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

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

294 ial media, alpha modification with 10% fetal bovine serum; SDS-PAGE, sodium dodecyl sulfate-polyacryl

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

296 Here, RFX1 overexpression reduced fetal bovine serum-stimulated proliferation of SH-SY5Y cells,

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

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

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

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