ライフサイエンスコーパス: bovine serum albumin

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

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

3 sed with tetraconazole haptens conjugated to bovine serum albumin.

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

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

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

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

8 e defined artificial target, i.e. acetylated bovine serum albumin.

9 n the side chain reduced the reactivity with bovine serum albumin.

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

11 ng of supercoiled plasmid DNA or cleavage of bovine serum albumin.

12 phosphine-derivatized fluorophore-conjugated bovine serum albumin.

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

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

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

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

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

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

19 e interactions, this study demonstrates that bovine serum albumin: 1) preferentially binds stressed o

20 n plasma volume after volume expansion (4.5% bovine serum albumin, 114 mul (g body wt)(-1) h(-1), 15

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

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

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

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

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

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

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

28 .0% (v/v) caproic acid (a lipid), 0.1% (w/v) bovine serum albumin and 0.01% (w/v) cytochrome C (both

29 a PACE separation, 46 tryptic peptides from bovine serum albumin and 150 putative neuropeptides from

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

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

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

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

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

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

36 ged SuDP and neutral SuVP were used to label bovine serum albumin and hemoglobin.

37 ed for 24 h in an enriched medium containing bovine serum albumin and increasing concentrations of pa

38 s, representative biological macromolecules (bovine serum albumin and methylcellulose), soot, natural

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

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

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

42 n of two common endocytic cargos: a protein, bovine serum albumin, and a lipid nanoparticle, low-dens

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

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

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

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

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

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

49 with three model organic foulants: alginate, bovine serum albumin, and Suwannee river natural organic

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

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

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

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

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

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

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

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

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

59 cilin at 18 nM was more effective than 1 muM bovine serum albumin at protecting DrdI from thermal ina

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

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

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

63 -laden model proteins (protein G, ovalbumin, bovine serum albumin, beta-galactosidase, lactoferrin) o

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

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

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

67 ot required for apoptosis because plating on bovine serum albumin-blocked poly-L-lysine (allows attac

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

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

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

71 f synthesized AgNPs, we used AgNPs to detect bovine serum albumin (BSA) and AgNPs-BSA composite nanop

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

73 he ability of grape seed extracts to bind to bovine serum albumin (BSA) and alpha-amylase was studied

74 ted for investigating the SEB specificity on bovine serum albumin (BSA) and avidin and detecting SEB

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

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

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

78 MS (LC-MS/MS) analysis of trypsin digests of bovine serum albumin (BSA) and HeLa cell lysate revealed

79 rescence microscopy (TIRFM), the dynamics of bovine serum albumin (BSA) and human fibrinogen (Fg) at

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

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

82 seinate (NaCas), whey protein isolate (WPI), bovine serum albumin (BSA) and lysozyme (Lys) were used

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

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

85 ple utility of cPILOT with in vitro nitrated bovine serum albumin (BSA) and mouse splenic proteins us

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

87 ng conditions, limited membrane digestion of bovine serum albumin (BSA) and subsequent ESI-Orbitrap M

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

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

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

91 In the present study, various forms of bovine serum albumin (BSA) are detected including therma

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

93 Using glycated bovine serum albumin (BSA) as a model protein of AGEs, w

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

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

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

97 Using Bovine Serum Albumin (BSA) as a surrogate for protein in

98 omavert and Miacalcin with a small amount of bovine serum albumin (BSA) as an impurity were analyzed.

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

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

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

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

103 SPNs were also synthesized and conjugated to bovine serum albumin (BSA) by carbodiimide-mediated chem

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

105 e antibodies that bind digoxin and a digoxin-bovine serum albumin (BSA) conjugate with high affinity

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

107 inkers, the labeling of the single available bovine serum albumin (BSA) cysteine residue was complete

108 presence of a complex and much more abundant bovine serum albumin (BSA) digest.

109 es of human choroid were incubated in C5a or bovine serum albumin (BSA) followed by quantitative immu

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

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

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

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

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

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

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

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

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

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

120 detection feasibility, surface adsorption of bovine serum albumin (BSA) is also analyzed.

121 Lumenal bovine serum albumin (BSA) lowered the lumenal ionic str

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

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

124 con by a chemical functionalization process, bovine serum albumin (BSA) molecules, were attached esse

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

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

127 ransepithelial electric resistance (TER) and bovine serum albumin (BSA) permeability assays.

128 and either hen egg white lysozyme (HEWL) or bovine serum albumin (BSA) produces the triplet state of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

161 nanopore, we detected long-lived captures of bovine serum albumin (BSA), a major multifunctional prot

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

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

164 onstrated with the use of standard peptides, bovine serum albumin (BSA), and human hemoglobin tetrame

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

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

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

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

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

170 oteins were consistently lower than those of bovine serum albumin (BSA), indicating that the use of B

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

200 d Con A in the presence of a large excess of bovine serum albumin (BSA).

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

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

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

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

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

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

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

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

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

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

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

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

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

214 erein, we report the fabrication of protein (bovine serum albumin, BSA) particles which were rendered

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

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

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

218 azole (PPT) as well as by a cell-impermeable bovine serum albumin conjugate of 17betaE2.

219 Bovine serum albumin-conjugated CORT reproduced the CORT

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

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

222 for 20 hours with SDF-1alpha (100 ng/mL) or bovine serum albumin (control).

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

224 s via a facile, green method using denatured bovine serum albumin (dBSA) as a stabilizing agent.

225 PA toxin with no interference from human and bovine serum albumin, demonstrating it as a potential to

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

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

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

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

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

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

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

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

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

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

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

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

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

239 on an immunokinetic assay for an antibody to bovine serum albumin has been determined in model serum

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

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

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

243 peritoneal nIgM or phosphate-buffered saline/bovine serum albumin/immunoglobulin G (100 mug followed

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

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

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

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

248 Jnk2 were primed by injection of methylated bovine serum albumin (mBSA) in Freund's complete adjuvan

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

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

251 casein), protein mixtures of beta-casein and bovine serum albumin, milk, and human serum samples.

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

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

254 le tracking, we find that the degradation of bovine serum albumin occurs in an endo-lysosomal vesicle

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

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

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

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

259 gated to different carriers such as protein (bovine serum albumin or ovalbumin), amino-functionalized

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

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

262 molecules of oleate or up to 18 molecules of bovine serum albumin per iron oxide core were found to b

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

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

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

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

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

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

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

270 Permethylation of styrene oxide-modified bovine serum albumin released the two methylthiophenylet

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

272 Bovine serum albumin separates by pressure-driven flow w

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

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

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

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

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

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

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

280 ormed on oxidized Tau protein and acetylated bovine serum albumin to identify amino acid modification

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

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

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

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

285 ection of only 1 pmol of a tryptic digest of bovine serum albumin using an eluent flow rate of 55 muL

286 ns were increased by 10,12-CLA compared with bovine serum albumin vehicle in the adipocyte fraction a

287 Bovine serum albumin was also tested as a protein standa

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

289 The binding to acetylated bovine serum albumin was inhibited by acetylsalicylic ac

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

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

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

293 Bovine serum albumin was selected as sacrificial layer f

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

295 tive uptake of NO(2) by aerosolized protein (bovine serum albumin) was investigated in an aerosol flo

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

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

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

299 etry to demonstrate the use of self-quenched bovine serum albumin with standard fluorescence techniqu

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