ライフサイエンスコーパス: bovine serum albumin

1 phosphine-derivatized fluorophore-conjugated bovine serum albumin.

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

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

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

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

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

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

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

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

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

11 sed with tetraconazole haptens conjugated to bovine serum albumin.

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

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

14 ver nanoparticles in ethanolic solutions and bovine serum albumin.

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

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

17 n controlled hydrolysis and precipitation of bovine serum albumin.

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

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

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

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

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

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

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

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

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

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

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

29 .0% (v/v) caproic acid (a lipid), 0.1% (w/v) bovine serum albumin and 0.01% (w/v) cytochrome C (both

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

90 9, 1.25 mug/mL) after passive adsorption and bovine serum albumin (BSA) as a blocking agent generated

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

166 (2+) complex with a model transport protein, bovine serum albumin (BSA), have been explored by means

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

262 A bovine serum albumin pretreatment protocol was developed

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

288 Bovine serum albumin was also tested as a protein standa

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

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

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

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

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

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

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