ライフサイエンスコーパス: BSA

1 BSA (mainly native) increased the curcumin photodegradat

2 BSA 9 inhibited CaMKII activity with an IC(50) value of

3 BSA adsorption was maximum at pH 5, a value close to the

4 BSA and gelatin was effectively precipitated by HMW frac

5 BSA formed a complex with the ligands with stoichiometry

6 BSA lost the alpha-helix and gain beta-sheets in the sec

7 BSA was used as a model protein and its oxidation achiev

8 BSA-ddRADseq allowed cost-effective analysis of multiple

9 BSA/curcumin complex showed 1:1 stoichiometry, but the t

10 binding the gold surface was treated with 3% BSA before detection.

11 mprised 1.3 M DMSO, 0.1 M trehalose and 1.5% BSA; cell viability was similar to fresh controls (78.8%

12 e yeast proteins mixed at ratios of 1:5:1:5, BSA was detected at ratios of 0.94:2.46:4.70:9.92 when s

13 CORAD (0.64 and 0.56), EASI (0.56 and 0.50), BSA (0.52 and 0.45), NRS-itch (0.60 and 0.53), POEM (0.5

14 The impact of emulsifier types (Tween 80, BSA and quillaja saponins) on the formation of clove oil

15 800CW-BSA was intranasally administered to the mice in vivo, f

16 cent dye-labeled bovine serum albumin (800CW-BSA, used as a model agent).

17 The mean concentration of 800CW-BSA in the brainstem after FUSIN delivery decreased from

18 The accumulation of 800CW-BSA was low in the heart, lung, spleen, kidneys, and liv

19 The delivery outcome of 800CW-BSA was the highest at the brainstem when T(lag1) was 0.

20 ested to assess the biodistribution of 800CW-BSA.

21 d to quantify the delivery outcomes of 800CW-BSA.

22 s, the affinity immunoassay interaction at a BSA concentration of 1mug/ml for an Au/GO-COOH chip, an

23 ) on bovine serum albumin glycoxidation in a BSA-glucose model in vitro.

24 Formed Glass/ZnO-NRs/Protein-A/BSA&Anti-OTA structures were integrated within portable

25 tment with N,O-bis(trimethylsilyl)acetamide (BSA) and then PhFCl/NMM/AgNO(3).

26 ng to different putative ligands (acetylated BSA [AcBSA], zymosan, mannan, and LPS from Escherichia c

27 The addition of benzenesulfinic acid (BSA) to UV-C irradiated GA lowered (P < 0.05) its antimi

28 amino)phenylsulfonamide]-5-oxopentanoic acid-BSA (SA2-BSA) antigens toward polyclonal antibody (Ab-15

29 ell as the real-time changes of the adsorbed BSA during 24 h.

30 t through the addition of the crowding agent BSA, but not by sucrose polymers.

31 AL-BSA modified surfaces were characterized by X-ray photoe

32 rospun amyloid like-bovine serum albumin (AL-BSA) nanofibers on QCM surfaces.

33 Owing to the self-functionality of AL-BSA nanofibers, these modified QCM surfaces were directl

34 Bovine serum albumin (BSA) adsorption was studied at different pHs and ionic s

35 e, the introduction of bovine serum albumin (BSA) and antibody (Ab) enhanced the dispersity of the se

36 rdiac myoglobin (MYG), bovine serum albumin (BSA) and cardiac troponin T (cTnT), respectively.

37 Bovine serum albumin (BSA) and dextran varying in molecular weights were first

38 wo different proteins [bovine serum albumin (BSA) and gelatin], molecular weights, total phenolics, c

39 two model proteins- i) bovine serum albumin (BSA) and ii) beta-galactosidase (beta-gal), was investig

40 levant components like bovine serum albumin (BSA) and lipopolysaccharide.

41 ng alternate layers of bovine serum albumin (BSA) and tannic acid (TA) were tested as Lf encapsulatio

42 iron oxide-associated bovine serum albumin (BSA) and the factors that affected the proteolysis.

43 plex labeled sample of bovine serum albumin (BSA) and yeast lysates mixed at different ratios.

44 passive adsorption and bovine serum albumin (BSA) as a blocking agent generated a moderate sensitivit

45 clusters (AuNCs) using bovine serum albumin (BSA) as a protecting agent.

46 honic acid assay using bovine-serum albumin (BSA) as a protein model on the l-cysteine SAuNPs@GO hybr

47 rum albumin (HSA), and bovine serum albumin (BSA) as model target proteins.

48 alpha-lactalbumin, and bovine serum albumin (BSA) as well as the free C34-BSA were demonstrated using

49 e allowed reduction of bovine serum albumin (BSA) binding (63c, 63d).

50 ed hydrogels made from bovine serum albumin (BSA) by using polyelectrolytes such as polyethyleneimine

51 n isothiocynate (FITC) Bovine Serum Albumin (BSA) conjugate incorporated in the sheath and intermedia

52 ted from a solution of bovine serum albumin (BSA) digested by trypsin as an enzymatic model and from

53 altoside (DDM) protect bovine serum albumin (BSA) from unfolding in SDS.

54 SPME/GC indicated that bovine serum albumin (BSA) had the highest affinity toward safranal, with bind

55 of SA interaction with bovine serum albumin (BSA) has been investigated by multi-spectroscopic and mo

56 o release behaviour of bovine serum albumin (BSA) in chitosan-tripolyphosphate (TPP) hydrogel beads.

57 ) was used to thiolate Bovine serum albumin (BSA) in solution followed by chemical cross linking to a

58 fluorescently labeled bovine serum albumin (BSA) into the nanoslits; and fluorescence correlation sp

59 t proteome spiked with bovine serum albumin (BSA) over a 10-fold dynamic range.

60 of a trypsin-digested bovine serum albumin (BSA) sample provided narrow peaks, short dwell time, and

61 anocomposite including bovine serum albumin (BSA) template Cu nanoclusters (CuNCs@BSA) and single-wal

62 that the adsorption of bovine serum albumin (BSA) to aqueous gold colloids can be quantified with mol

63 oles in the ability of bovine serum albumin (BSA) to form stable nanostructures with bioactive molecu

64 molar ratio of IgG and bovine serum albumin (BSA) tryptic digest mixtures reached to 1:500.

65 denaturation degree of bovine serum albumin (BSA) was assessed.

66 e media modifications, bovine serum albumin (BSA) was identified as blocking initial cell-surface adh

67 YG) through binding to bovine serum albumin (BSA) was investigated at pH 3.0 using atomic force micro

68 ver, the adsorption of bovine serum albumin (BSA) was significantly reduced at the SR coated ion-sele

69 between Allura Red and bovine serum albumin (BSA) was studied in vitro at pH 7.4.

70 EDC-NHS chemistry and Bovine serum albumin (BSA) was used for blocking of the non-specific binding s

71 bumin (alpha-Lac), and bovine serum albumin (BSA) were bound to beta-C with overall binding constant

72 ibodies against native bovine serum albumin (BSA) were detected.

73 a post-treatment with bovine serum albumin (BSA) which served as the blocking agent to prevent non-s

74 stepwise unfolding of bovine serum albumin (BSA) with guanidine hydrochloride (GuHCl) has been inves

75 (TI); Ovalbumin (OVA); Bovine Serum Albumin (BSA)), we observe resolution of the markers in <60 s, wi

76 t different rates with bovine serum albumin (BSA), a molecular substitute for detritus.

77 tube compartments with bovine serum albumin (BSA), GDNF and NGF increased the motor and sensory axon

78 del transport protein, bovine serum albumin (BSA), have been explored by means of different spectrosc

79 drogels has focused on bovine serum albumin (BSA), leaving human serum albumin (HSA) comparatively un

80 film and adsorption of bovine serum albumin (BSA), respectively, on poly(methyl methacrylate) (PMMA)

81 Bovine serum albumin (BSA), whey protein isolate (WPI), insulin and a casein h

82 from the model protein bovine serum albumin (BSA).

83 othreat scenario using bovine serum albumin (BSA).

84 inherent biocompatible bovine serum albumin (BSA).

85 d heat-set gelation of bovine serum albumin (BSA).

86 r were backfilled with bovine serum albumin (BSA).

87 Bovine serum albumin (BSA)/curcumin binding and dye photodegradation stability

88 (glycerol) and large (bovine serum albumin; BSA) analyte molecules, indicating that the hydrogel wav

89 Bulked segregant analysis (BSA) is used to identify existing or induced variants th

90 ene copies, we used bulk segregant analysis (BSA) of radiation hybrid (RH) cells.

91 method, followed by bulk segregant analysis (BSA) to identify large-effect QTLs.

92 A bulk segregant analysis (BSA) version of double-digest restriction-site associate

93 Bulked segregant analysis (BSA), coupled with next-generation sequencing, allows th

94 ed at pH 3 compared to pH 7, although AH and BSA respectively undergo repulsive and attractive electr

95 antly associated with MM, even after BMI and BSA adjustments.

96 ges of individual proteins (cytochrome C and BSA) as well as of protein complexes (hemoglobin), which

97 tions in the amino acid sequences of HSA and BSA exist; these account for differences in the hydrogel

98 ion methods are usually employed for HSA and BSA, and variations in the amino acid sequences of HSA a

99 We detected no binding to mannan and BSA.

100 The interaction between MC and BSA was more favorable than with CA and was enthalpicall

101 nhibitors of AGEs in BSA-GLU (7.20mg/mL) and BSA-MGO (9.53mg/mL) models.

102 h in next steps was modified by anti-OTA and BSA in this way a anti-OTA/Protein-A/PSi structure sensi

103 zed as a function of pH, ionic strength, and BSA concentration using in-situ Attenuated Total Reflect

104 Thiolates and BSA were more efficient at ligand exchange than amine-co

105 arameters depended on the technique used and BSA conformation.

106 g concentrations of chitosan (1-2.5%w/w) and BSA (0.25-10%w/w) into TPP solutions ranging in concentr

107 76 +/- 6% and 85 +/- 2%, for (BSA-TA)4 and (BSA-TA)8 shells, respectively.

108 ation of bovine serum albumin antibody (anti-BSA) and fibrinogen antibody (anti-Fg) onto the pCB-coat

109 gnaling mechanisms, we intrathecally applied BSA-conjugated E2 over the spinal phrenic motor nucleus

110 static quenching due to the formation of AR-BSA complex, with binding constant (K) ranging from 3.26

111 cial tension measurements showed that the AR-BSA complex presented surface activity, since interfacia

112 % or more of their facial body surface area (BSA) and 3% or more of their non-facial BSA were randoml

113 measurements adjusted for body surface area (BSA) and stratified by age, sex, race, and ethnicity.

114 ht (kg)/height (m)2), and body surface area (BSA) at ages 7-13 years and birth weight are associated

115 and end-diastolic volume/body surface area (BSA) were 62 (45-101) and 104 (83-143) mL/m(2), respecti

116 Body surface area (BSA)-adjusted chronic kidney disease epidemiology (CKD-E

117 LVDV) was 40 mL (LVDV per body surface area [BSA], 25 mL/m(2)); left ventricular end-systolic volume

118 between clinical measures (body surface area/BSA, pruritus ADQ, and transepidermal water loss/TEWL) w

119 (QTL), and this technique is referred to as BSA-Seq here.

120 rotease hydrolyzed the iron oxide-associated BSA directly at the surface without an initial desorptio

121 Fast initial rates of iron oxide-associated BSA proteolysis, comparable to proteolysis of BSA in sol

122 ggregation of biotinylated contrast agent (b-BSA-Gd-DTPA).

123 n, and recycling associated with the large b-BSA-Gd-DTPA conjugate.

124 from pregnant mice after administration of b-BSA-Gd-DTPA and analyzed using a new sub-voxel biophysic

125 e transporters with free biotin suppressed b-BSA-Gd-DTPA uptake.

126 Within this complex proteomics background, BSA spiked at 1:5:10 ratios was detected at ratios of 1.

127 nerated four families of benzenesulfonamide (BSA) derivatives for SAR analysis.

128 otein-SDS complexes and refolding of betaLG, BSA, and lysozyme, while alphaLA changed to its NIS-boun

129 tes to the knowledge of interactions between BSA and azo colorants under physiological conditions.

130 serum albumin (BSA) as well as the free C34-BSA were demonstrated using none or single enzyme digest

131 At pH 7.4, CA-BSA complex formation was entropically driven.

132 a large data set from patients with cancer, BSA-adjusted CKD-EPI is the most accurate published mode

133 on carbon nanotube-bovine serum albumin (CNT-BSA) hybrid system, by which sensitivity and detection l

134 e lateral flow assay the channel combination BSA was found optimum (mean average error = 36% +/- 6%;

135 c paper strips with the pyridoxal conjugated BSA-AuNCs for detecting Hg(2+) ion up to 1nM.

136 Constructed BSA-agarose columns could extract OTA efficiently from r

137 e the immunosensor, abbreviated as anti-cTnI(BSA)/NAC-CdAgTe QDs/AuNPs/GCE.

138 lbumin (BSA) template Cu nanoclusters (CuNCs@BSA) and single-walled carbon nanotubes (SWCNT) was synt

139 model based on bovine serum albumin-water (D(BSA/w)) and liposome-water distribution ratios (D(lip/w)

140 ng in the presence of NaCl and for denatured BSA/lutein binding.

141 The efficiency of different BSA-dextran conjugates was systematically studied to pre

142 d continuous gelatin networks with dispersed BSA inclusions whereas pressurization at 80 degrees C yi

143 ized conjugates of bovine serum albumin (DNP-BSA) or mobile in a supported lipid bilayer (DNP-SLB).

144 application of the membrane-impermeable E2 (BSA-conjugated E2; 15 min).

145 significantly higher oSCORAD, SCORAD, EASI, BSA, NRS-itch, POEM, and DLQI (P < .0001 for all).

146 nsequent higher BSA surface loading enhanced BSA adsorption by protein-protein interaction, which les

147 rea (BSA) and 3% or more of their non-facial BSA were randomly assigned (1:1:1:1:1) by use of an inte

148 iocyanate-labeled bovine serum albumin (FITC-BSA).

149 resolution exceeding 1.0 and CVs of 8.4% for BSA-OVA and 2.4% for OVA-TI, with comparable reproducibi

150 veloped a simple and effective algorithm for BSA-Seq data analysis and implemented it in Python; the

151 SNP index method and G-statistic method for BSA-Seq data analysis require relatively high sequencing

152 The opposite was observed for BSA/lutein binding in the presence of NaCl and for denat

153 metry (1:1), and thermodynamic potential for BSA/lutein binding were independent of protein conformat

154 The results for BSA on gold colloid nanoparticles can be modeled in term

155 used a pH decrease of 3.1 and 2.7 units (for BSA and beta-gal, respectively) attributed to selective

156 as found to be 76 +/- 6% and 85 +/- 2%, for (BSA-TA)4 and (BSA-TA)8 shells, respectively.

157 scaffolds for producing arrays of functional BSA biogratings on low energy surfaces by a water-assist

158 y is compatible with multiple proteins (e.g. BSA, HSA, GOx, beta-galactosidase) and monomer classes i

159 Finally, the scope of Gel-BSA-OHG substrate-based ELISA for clinical application w

160 The stability and ELISA performance of Gel-BSA-OHG was evaluated in comparison to the conventional

161 hypothesis using GelNP-based substrate (Gel-BSA-OHG) to adhere 8-hydroxy-2'-deoxyguanosine (8-OHdG)

162 Importantly, the Gel-BSA-OHG substrate was found to be more wash-resistant an

163 After activation of carboxylic groups, BSA was immobilized onto the CMD chip through covalent a

164 and the use of structurally unrelated hapten-BSA adducts confirmed antigen specificity.

165 n quantification: butanol/HCl, vanillin/HCl, BSA/FeCl(3) and PVPP/Folin-Ciocalteu.

166 noncovalent surface treatments (PEGMA, HEMA, BSA, O(2) plasma) on our blood filter and their effect o

167 BSA concentration and the consequent higher BSA surface loading enhanced BSA adsorption by protein-p

168 PP concentration of 0.4% w/w had the highest BSA entrapment efficiency (71.6+/-0.7%) and inhibited BS

169 tion of human serum:bovine serum albumin (HS:BSA) mixtures onto the folic acid modified sensor result

170 wo fluorescently-tagged proteins, i.e., IgG, BSA, on surfaces with different hydrophobicity and chemi

171 AP and AS binding to immobilized BSA at different concentrations was assessed.

172 ponse studies of fabricated immunoelectrode (BSA/anti-CYFRA-21-1/APTES/nHfO2@RGO/ITO) revealed higher

173 id receptor (mbGR) by using cell-impermeable BSA-conjugated dexamethasone.

174 s were the most potent inhibitors of AGEs in BSA-GLU (7.20mg/mL) and BSA-MGO (9.53mg/mL) models.

175 ould detect SP lysate even when dispersed in BSA or Escherichia coli lysate.

176 layers and an impressive 30-fold increase in BSA permeability.

177 itu labeling of a buried cysteine residue in BSA during extensional stress.

178 The pH played an important role in BSA conformation, which altered the manner in which it i

179 ttering experiments verified that individual BSA monomers in bulk solution had increasingly lower con

180 pment efficiency (71.6+/-0.7%) and inhibited BSA release in simulated gastric fluid (SGF) to a greate

181 TR-FTIR spectra revealed that higher initial BSA concentration and the consequent higher BSA surface

182 enzymatic model and from solutions of intact BSA and trypsin.

183 eine SAuNPs@GO hybrid exhibited 80.57% lower BSA fouling compared with that of the cysteamine SAuNPs@

184 yridoxal was conjugated with the luminescent BSA-AuNCs through the free amines of BSA and then employ

185 ular end-systolic volume (LVSV), 21 mL (LVSV/BSA, 13 mL/m(2)); stroke volume (SV), 19 mL (SV/BSA, 12

186 ng to ~ 80% lower sequencing cost and making BSA-Seq more accessible to the research community and mo

187 to endocytose rhodamine-labeled mannosylated BSA (rMBSA), though the receptor was not involved in the

188 increasing RV end-diastolic volume/BSA, mass/BSA, and pulmonary arterial stiffness, and with decreasi

189 Eed increased with increasing RV mass/BSA, end-diastolic volume/BSA, and T1 mapping and with d

190 se data contribute to the knowledge of CA/MC-BSA interactions and provide important data for applicat

191 s, zymosan-induced arthritis, and methylated BSA/IL-1 arthritis by both prophylactic and therapeutic

192 A new G-CSF-driven (methylated BSA/G-CSF) arthritis model was established enabling us t

193 Mean CKD-EPI eGFR was 42 mL/min/BSA and median [IQR] uACR was 3 [11] mg/mmol.

194 omerular filtration rate (eGFR) <= 60 mL/min/BSA) (n = 118), we collected clinical and longitudinal l

195 nual CKD-EPI eGFR decreased by - 0.56 mL/min/BSA/year for each logarithm unit increase in baseline uA

196 For native BSA/curcumin, fluorescence indicated an enthalpic and en

197 the morphology of a network made with native BSA molecules being crosslinked with genipin at ambient

198 ophenylacetyl (NIP)-specific IgE JW8 and NIP-BSA to assess binding, uptake, and degradation dynamics.

199 ed by extensional flow on the aggregation of BSA, beta2-microglobulin (beta2m), granulocyte colony st

200 ucts, and resisted structural alterations of BSA subjected to glycation.

201 nescent BSA-AuNCs through the free amines of BSA and then employed for the nanomolar detection of Hg(

202 The partial molar volume changes of BSA and Tg at the maximal investigated pressure and mini

203 er, the enthalpic and entropic components of BSA/lutein binding in the presence of NaSCN decreased as

204 Eight cysteines of HSA and four cysteines of BSA have been detected to react with NAPQI.

205 The net increase in T(d) of BSA was linearly correlated with the net increase in gel

206 Complete denaturation of BSA occurred only when the gelation temperature (T(G)) w

207 the surface without an initial desorption of BSA.

208 further used to investigate the diffusion of BSA in the nanoslits.

209 0 degrees C yielded an inverse dispersion of BSA as the continuous phase supporting liquid gelatin in

210 rough quenching of intrinsic fluorescence of BSA.

211 d CYG molecules were found at the site II of BSA with combined static and dynamic quenching mechanism

212 led beta-C was bound to the subdomain IIA of BSA, the residues of aromatic cluster II in alpha-lactal

213 tein was preferentially bound to site III of BSA.

214 succinimide (MTS/GMBS) for immobilization of BSA-MC-LR conjugate, which was confirmed to have uniform

215 We studied the influence of BSA unfolding and those of two Hofmeister salts, sodium

216 endocytosis and degradation in lysosomes of BSA.

217 SA proteolysis, comparable to proteolysis of BSA in solution, and very slow rates at prolonged proteo

218 re measured across a 10-fold mixing range of BSA in a background of yeast proteome.

219 Inhibited release of BSA, in both SGF and SIF, was achieved with low PPA conc

220 Removal of BSA allowed for the first time observation of Lcr biofil

221 The dose-response sensorgrams of BSA upon increasing concentration of AP and AS have been

222 4)L.mol(-1), at the warfarin binding site of BSA.

223 g study demonstrated that A binding sites of BSA play the main role in the interaction with acetate.

224 d MC had no effect on the surface tension of BSA/air interfaces.

225 Echocardiographic Z scores based on BSA were derived from a large, diverse, and healthy Nort

226 sodium thiocyanate (NaSCN) as chaotrope, on BSA/lutein binding at pH 7.4 using fluorescence spectros

227 y distributed without residual dependence on BSA.

228 , without any comparable influence of BMI or BSA.

229 A single dose of leptin (0.4 mg/kg) or BSA (vehicle) were administered intranasally or intraper

230 umins, particularly that from bovine origin (BSA), have stable binding affinity towards some mycotoxi

231 High selectivity (1:1200, ovalbumin/BSA) and detection limit of 100 attomole is attained for

232 avior of DNPH and of the native and oxidized BSA was investigated in solution.

233 tein and detection limits of 50 mug oxidized BSA and 0.75 pmol carbonyls.

234 nti-IgGNPs as sensing nanobioprobe, MB-p53Ag/BSA as a nanomagnetic bead, and microwell ELISA plate, M

235 nomagnetic beads, blocked with BSA (MB-p53Ag/BSA) for capture and separation.

236 ely isolated and purified using the MB-p53Ag/BSA.

237 c bead, and microwell ELISA plate, MTP-p53Ag/BSA were compared.

238 hed the stimulation of sodium palmitate (PA)-BSA on Nox2 gene expression.

239 A piperacillin-BSA adduct was used as an antigen in ELISA antibody bind

240 A piperacillin-BSA adduct with cyclized and hydrolysed forms of the hap

241 cted with antigens generated at piperacillin/BSA ratios of 10:1 and above, which corresponded to a mi

242 rease in stiffness induced by PEI to program BSA hydrogels in various shapes.

243 orption of the broadly studied model protein BSA onto the hematite mineral surface was characterized

244 Four proteins, BSA, alpha-lactalbumin (alphaLA), lysozyme, and beta-lac

245 ivergent properties were displayed by the RH-BSA growth genes compared to those from loss-of-function

246 end-diastolic volume (RVDV) was 262 mL (RVDV/BSA, 164 mL/m(2)); right ventricular end-systolic volume

247 lar end-systolic volume (RVSV), 198 mL (RVSV/BSA, 124 mL/m(2)); stroke volume (SV), 64 mL (SV/BSA, 40

248 Afterward, SA2-BSA was covalently bonded to Py/Py-COOH/MNP modified gol

249 nylsulfonamide]-5-oxopentanoic acid-BSA (SA2-BSA) antigens toward polyclonal antibody (Ab-155).

250 of four spiked proteins in E. coli samples, BSA, beta-lactoglobulin, alpha-casein, and alpha-lactalb

251 restriction-site associated DNA sequencing (BSA-ddRADseq) was developed and used to detect and posit

252 fluorescein, and ~ 120% for larger solutes, BSA and Dex-70k.

253 egatively charged globular protein solution (BSA) can either cause simple adsorption on a negatively

254 in comparison to the conventional substrate (BSA-OHG).

255 , 13 mL/m(2)); stroke volume (SV), 19 mL (SV/BSA, 12 mL/m(2)); and ejection fraction, 47%.

256 124 mL/m(2)); stroke volume (SV), 64 mL (SV/BSA, 40 mL/m(2)); and ejection fraction, 24%.

257 transform infrared (FTIR) demonstrated that BSA entrapped in the nanocomposite film have been change

258 Furthermore, we found that BSA had a moderate positive effect for the TaqMan Univer

259 The BSA/lutein complex formation was entropically driven and

260 and 3D water structure directly affected the BSA/lutein binding thermodynamics.

261 20% to 14.17% in contrast to 18.62% for the BSA-adjusted CKD-EPI and 25.51% for the Cockcroft-Gault

262 f the BSA binding sites were occupied in the BSA-CYG complex through hydrogen bonds and van der Waals

263 was the most potent inhibitor of AGEs in the BSA-GLU model (6.52 mg/mL on average) relative to other

264 Among all samples assayed in the BSA-MGO model (61.97-14.48 mg/mL), HHP-treated 'Weiki' (

265 f preadsorbed phosphate or by increasing the BSA coverage, which prevented protease adsorption.

266 Approximately 93% of the BSA binding sites were occupied in the BSA-CYG complex t

267 YG molecules caused partial unfolding of the BSA structure, while it was not enough for significant a

268 The efficacy of the BSA-based method was further validated by direct compari

269 s followed by Layer-by-Layer assembly of the BSA-TA shells and dissolution of the CaCO3 cores was sug

270 ing interfacial architecture is based on the BSA-E2 conjugate within the BSA matrix immobilized on th

271 Increasing TPP concentration or the BSA concentration loaded, led to early release in SGF.

272 Therefore, the BSA conformation and 3D water structure directly affecte

273 on was maximum at pH 5, a value close to the BSA isoelectric point (~ pH 5), and lower at pH 4 and pH

274 (34.78%) at pH 3.0 was mainly driven via the BSA-hemiketal association, although the colored species

275 is based on the BSA-E2 conjugate within the BSA matrix immobilized on the "charged" (as a result of

276 naerobic germination were identified through BSA.

277 onfirmed the interaction of this additive to BSA.

278 s to amine-tagged single-stranded DNA and to BSA protein demonstrate the potential of SOF(4) -derived

279 The KD value for binding of AP and AS to BSA were 4.09x10(-5) and 1.89x10(-5), at 25 degrees C.

280 D) showed high affinity of both AP and AS to BSA.

281 isrupted the Kindlin-2(+/-) MAECs barrier to BSA and dextran and reduced transendothelial resistance

282 showed that AP and AS molecules can bind to BSA.

283 posed to 0.4 mm oleic acid (OA) complexed to BSA.

284 The high affinity of SA to BSA was demonstrated by a binding constant value (1.09x1

285 antigen (f-PSA), which is similar in size to BSA, were performed to validate the trapping of the mole

286 ions constituting 20% or less of their total BSA for 24 weeks.

287 Increasing ionic strength decreased to total BSA adsorption.

288 pecies of CYG had a greater affinity towards BSA in the equilibrated system at pHs 1.0 and 5.0.

289 enyl mAbs and challenged with trinitrophenyl-BSA intravenously to induce systemic anaphylaxis that wa

290 nges in dissolved oxygen (DO) and undigested BSA concentration were monitored during enrichment and r

291 Thus, this work used BSA immobilized in agarose beads as a novel solid-phase

292 increasing RV mass/BSA, end-diastolic volume/BSA, and T1 mapping and with decreasing EF.

293 ased with increasing RV end-diastolic volume/BSA, mass/BSA, and pulmonary arterial stiffness, and wit

294 ilized onto nanomagnetic beads, blocked with BSA (MB-p53Ag/BSA) for capture and separation.

295 obody by an order of magnitude compared with BSA.

296 nteraction of SA and its Cu(2+) complex with BSA occurred through quenching of intrinsic fluorescence

297 PI values were significantly correlated with BSA-MGO, anti-ACE, anti-AChE and PCLACW parameters.

298 l/HCl and vanillin/HCl were higher than with BSA/FeCl(3) and PVPP/Folin-Ciocalteu.

299 Antibodies together with BSA (forming the whole biorecognition layer) served to s

300 score models involved indexed parameters (X/BSA(alpha)) that were normally distributed without resid