ライフサイエンスコーパス: BSA

1 BSA (mainly native) increased the curcumin photodegradat

2 BSA and gelatin was effectively precipitated by HMW frac

3 BSA formed a complex with the ligands with stoichiometry

4 BSA was found to exhibit a maximum degree of heat denatu

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

6 n (25 - 75% range, mug/mmol creatinine x m(2)BSA).

7 (-33.0/-13.2/-2.3), EASI (-17.1/-9.8/-3.2), BSA (-46%/-15%/-4%), NRS-itch (-5/-2/0), POEM (-5/-2/0),

8 , 2-octynoic acid (2-OA) coupled to BSA (2OA-BSA) and evaluated the natural history of subsequent dis

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

10 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

11 A BSA layer was cross-linked around the polymer, resulting

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

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

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

15 Warfarin dose was influenced by age, BSA, CKD, amiodarone use, and CYP2C9*3 and VKORC1 varian

16 s serving as an effective exfoliating agent, BSA can also function as a strong stabilizing agent agai

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

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

19 sage of these self-functional electrospun AL-BSA infrastructure sensing layers on QCM surfaces.

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

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

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

23 with various proteins (bovine serum albumin (BSA) and different forms of hemoglobin).

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

25 lity, albumins such as bovine serum albumin (BSA) and human serum albumin (HSA) have found a wide ran

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

27 del system composed of bovine serum albumin (BSA) and methylglyoxal (MGO).

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

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

30 nsing of biomolecules (bovine serum albumin (BSA) as reference) binding to gate-immobilized anti-BSA

31 tion of CA and MC with bovine serum albumin (BSA) at pH 3.5, 5.0, and 7.4 using fluorescence spectros

32 y during adsorption of bovine serum albumin (BSA) at the surface of the K(+)-ISEs.

33 s of interest, such as bovine serum albumin (BSA) concentration, incubation times and labeled antibod

34 mitate (50 mumol/L) or bovine serum albumin (BSA) for 24 hr.

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

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

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

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

39 ion (UF) membranes and bovine serum albumin (BSA) over a range of ionic strengths.

40 tylcholine (ACh) using bovine serum albumin (BSA) protected atomically precise clusters of gold.

41 on and denaturation of bovine serum albumin (BSA) protein onto a silica-coated array of plasmonic gol

42 on by cyclodextrins or bovine serum albumin (BSA) results in a nonhomogeneous solvation shell that is

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

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

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

46 ate a method that uses bovine serum albumin (BSA) to control the receptor-accessible part of rebaudio

47 ater by using protein, bovine serum albumin (BSA) to produce single-layer nanosheets, which cannot be

48 , we choose to monitor bovine serum albumin (BSA) unspecific adsorption, which has been often employe

49 etween glutathione and bovine serum albumin (BSA) using ultraviolet-visible (UV-vis) absorption, fluo

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

51 In this system, bovine serum albumin (BSA) was immobilized on gold grids as the enzymatic subs

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

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

54 electrode covered with Bovine Serum Albumin (BSA) was used for the control of non-specific currents.

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

56 ted the interaction of bovine serum albumin (BSA) with AP and AS using surface plasmon resonance (SPR

57 out the hydrolysis of bovine serum albumin (BSA) within 1h, and the assay was performed by using liq

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

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

60 After conjugation to bovine serum albumin (BSA), glycoconjugates 1 to 6 were used to develop indivi

61 ng chymotrypsin (chy), bovine serum albumin (BSA), lysozyme (lyz) and cytochrome c (cyt c) in singula

62 specific adsorption of bovine serum albumin (BSA), or specific lectin binding on glycopolymer brushes

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

64 ut spiked additions of Bovine Serum Albumin (BSA), showed considerable disagreement.

65 e hydrolase (ELP-OPH), bovine serum albumin (BSA), titanium dioxide nanofibers (TiO2NFs) and carboxyl

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

67 d free HSA (ffHSA) and bovine serum albumin (BSA).

68 ocyanidin oligomers to bovine serum albumin (BSA).

69 annin precipitation by bovine serum albumin (BSA).

70 er antigen CA-15.3 and bovine serum albumin (BSA).

71 for the model protein bovine serum albumin (BSA).

72 -lactalbumin (ALA) and bovine serum albumin (BSA).

73 to the amino groups of bovine serum albumin (BSA).

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

75 othreat scenario using bovine serum albumin (BSA).

76 inherent biocompatible bovine serum albumin (BSA).

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

78 s was evaluated in the bovine serum albumin (BSA)/glucose system.

79 ed tryptic digest with bovine serum albumin (BSA:casein, 100:1).

80 y interaction between bovine serum albumine (BSA) with anti-BSA antibody (AB) as a model system, we b

81 hia coli bacteria and bovine serum albumine (BSA).

82 Although BSA conversion equations have been used in certain clini

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

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

85 mM, there was a decrease in the PVDF-BSA and BSA-BSA electrostatic repulsion forces, resulting in a h

86 which caused a decrease in the PVDF-BSA and BSA-BSA interaction forces accompanied by a decreased hy

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

88 GPER antagonist G-15 attenuated DHEA- and BSA-conjugated DHEA-stimulated pri-miR-21 transcription.

89 es of KSV, Ka and Kb for the glutathione and BSA interaction were in the order of 10(5).

90 Also, the interaction of glutathione and BSA was spontaneous.

91 with two homologous serum proteins, HSA and BSA, were investigated, employing microcalorimetric tech

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

93 ponsible for the associations of obesity and BSA with thyroid cancer.

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

95 arameters depended on the technique used and BSA conformation.

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

97 76 +/- 6% and 85 +/- 2%, for (BSA-TA)4 and (BSA-TA)8 shells, respectively.

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

99 The binding coefficient for BSA-anti-BSA interaction shows a behavior corresponding to the La

100 reference) binding to gate-immobilized anti-BSA antibodies and analyzed using the Langmuir binding t

101 etween bovine serum albumine (BSA) with anti-BSA antibody (AB) as a model system, we built the PEC im

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

103 Appropriate BSA transformations (BSA(alpha)) were selected for each

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

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

106 at each level to patient body surface area (BSA) and sex.

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

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

109 Body surface area (BSA) scaling has been used for prescribing individualize

110 nine, sex, age, race, and body surface area (BSA) were significantly associated with the likelihood o

111 participants with a high body surface area (BSA), great height, or excess weight and for women with

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

113 effect of clinical (age, body surface area [BSA], chronic kidney disease [CKD], and amiodarone use)

114 eed, gold cluster bovine serum albumin (AuNC@BSA) nanogates were engineered on mesoporous silica nano

115 wt%), was bound with negatively-charged AuNC@BSA electrostatically-attached onto MSN-NH3(+), affordin

116 trategies used to cap the pores of MSN, AuNC@BSA nanogates are biotools and were applied for targeted

117 fording highly loaded pH-responsive MSN-AuNC@BSA nanocarriers.

118 The gold quantum clusters (AuQC@BSA) synthesized using bovine serum albumin and conjugat

119 pecific for acetylcholine, resulting in AuQC@BSA-AChE.

120 The fluorescent intensity of AuQC@BSA-AChE is sensitive towards acetylcholine in range of

121 Further, the sensor, AuQC@BSA-AChE can be easily coated on paper and an efficient

122 This suggests that AuQC@BSA-AChE has an excellent potential to be used for diagn

123 oline (Ch) which in turn interacts with AuQC@BSA-AChE and quenches its fluorescence, enabling sensing

124 ve area normalized to body surface area (AVA/BSA) <0.6 cm(2)/m(2); yet, this cutoff has never been va

125 usted HR, 2.18 [1.28-3.71]), followed by AVA/BSA <0.40 cm(2)/m(2) (adjusted HR, 1.84 [1.09-3.11]), AV

126 ds, AVA/height <0.45 cm(2)/m followed by AVA/BSA <0.40 cm(2)/m(2) seem as robust parameters for defin

127 howed better predictive performance than AVA/BSA with improved reclassification and better discrimina

128 High risk of events was observed with AVA/BSA <0.4 cm(2)/m(2) (adjusted hazard ratio [HR], 3.42 [2

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

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

131 otein-A/Anti-OTA was additionally blocked by BSA.

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

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

134 y is achieved up to 1:8500 using beta-casein/BSA mixture and sensitivity down to 1 atto-mole.

135 proximately 705.1, 6.5, 6.4 and 5.1 for chy, BSA, lyz and cyt c, respectively.

136 This FITC-conjugated BSA acted as a template for the synthesis of red-emittin

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

138 Consequently, BSA passed more easily through the membrane and into per

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

140 r that included linear, quadratic, and cubic BSA terms and a sex main effect as independent variables

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

142 In the prepared nanocomposite, the CuNCs@BSA found to play as a conductive holder as well as an a

143 d is delivered as a complex with delipidated BSA (2:1, mol/mol) and does not induce significant lipot

144 brane surface, and the formation of a denser BSA layer; consequently, membrane fouling was enhanced.

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

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

147 ilonRI) and stimulated using the antigen DNP-BSA.

148 rm for DNP-SLB and edge-concentrated for DNP-BSA.

149 entional liposome containing gadolinium-DTPA-BSA lipid.

150 differences in physiological factors (i.e., BSA) as well as use of personal care products containing

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

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

153 lated fluorescent-bovine serum albumin (FITC-BSA) inside the gel.

154 links and instantaneously liberates the FITC-BSA under 2 cm thick tissue.

155 excitation, FITC/BSA-stabilized AuNCs (FITC/BSA-AuNCs) emitted fluorescence at 525 and 670nm, which

156 ced change in FITC fluorescence enabled FITC/BSA-AuNCs to detect an ammonia product-related enzyme sy

157 ence quenching of AuNCs by H2O2 enabled FITC/BSA-AuNCs to ratiometrically detect the H2O2 product-rel

158 Under single wavelength excitation, FITC/BSA-stabilized AuNCs (FITC/BSA-AuNCs) emitted fluorescen

159 uNCs were used as an internal standard, FITC/BSA-AuNCs offered a sensitive and reversible ratiometric

160 ld nanoparticles (PVP-AuNPs) and fluorescent BSA-protected gold nanoclusters (BSA-AuNCs) were used as

161 o influence the emission of the fluorophore, BSA-AuNCs, in the IFE-based fluorescent assays.

162 For BSA binding at the surface, EIS sensor signals mainly co

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

164 as the Cockcroft-Gault equation adjusted for BSA, followed by Cockcroft-Gault equation, and CKD-EPI e

165 The binding coefficient for BSA-anti-BSA interaction shows a behavior corresponding

166 The obtained binding coefficients for BSA are found to be same as in results from literature,

167 demonstrate that recent recommendations for BSA are not appropriate for animal-to-human dosage conve

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

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

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

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

172 Ps deposition was in order of SA > HA > TA > BSA.

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

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

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

176 In order to immobilize BSA, carboxymethyl dextran hydrogel (CMD) Au chip was us

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

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

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

180 We found that membrane-impermeable BSA-conjugated P4 inhibited primordial follicle formatio

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

182 Moreover, glutathione was docked in BSA using ArgusLab as a molecular docking program.

183 ayers and an impressive 30-fold increase in BSA permeability.

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

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

186 e results because it reduced with increasing BSA concentration.

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

188 alcium ions into the mixture of heat-induced BSA nano-aggregates and pristine BSA molecules at room t

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

190 C x muFFE analysis of a Chromeo P503-labeled BSA tryptic digest produced a 2D separation that made ef

191 chieved in 4T1 breast cancer with (64)Cu-LDH-BSA via passive targeting alone (7.7 +/- 0.1%ID/g at 16

192 , we report that glutaraldehyde cross-linked BSA (or HSA) forms a novel fluorescent biological hydrog

193 The BSA-gold nanoclusters/ionic liquid (BSA-AuNCs/IL) was used as a suitable nanocomposite platf

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

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

196 hout ENT examination are as follows: maximal BSA detachment (20% [0%-95%] vs 5.5% [0%-95%]; P = .004)

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

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

199 Arthritis was induced by methylated BSA (mBSA) in mBSA-sensitized wild-type (WT), Ido1(-/-),

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

201 ypersensitivity (DTH) response to methylated BSA and generation of Th17 cells while promoting Tregs.

202 T) measurements with co-existed 10 microg/ml BSA interference.

203 fluorescent BSA-protected gold nanoclusters (BSA-AuNCs) were used as an IFE absorber/fluorophore pair

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

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

206 There was less accumulation of BSA on the membrane surface.

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

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

209 yer structure was formed by self-assembly of BSA-dextran micelles to envelope solid lipid via a pH- a

210 teraction forces, the adsorption behavior of BSA on the membrane surface, and the structure of the BS

211 ion containing trypsin, the peptide bonds of BSA were hydrolyzed and peptide fragments were desorbed

212 adius and increased diffusion coefficient of BSA.

213 ssing strategy enables reliable detection of BSA at concentrations in the range from 150 pM to 15 muM

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

215 izes as well as for the monomer and dimer of BSA and an antibody.

216 bsorption of PVP-AuNPs and the excitation of BSA-AuNCs.

217 ing obtained was related to the formation of BSA-glutathione complex.

218 a decrease in available free amino groups of BSA in presence and absence of MGO, suggesting the simul

219 in the sub-domain IIA pocket in domain II of BSA.

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

221 an increase in the fluorescence intensity of BSA upon increasing the amounts of SA.

222 indicated that the fluorescence intensity of BSA was decreased considerably upon the addition of glut

223 The loss of BSA fragments and the enhancement of Au photoelectron si

224 nduced significant fluorescence quenching of BSA-AuNCs.

225 es, resulting in a higher deposition rate of BSA onto the membrane surface, and the formation of a de

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

227 idase (ChOx) by the fluorescence response of BSA-AuNCs.

228 form for the immobilization and retention of BSA proteins in the microbial-protective environments.

229 , we provide further evidence of the role of BSA and excess weight in the risk of thyroid cancer.

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

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

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

233 diterpene of Reb A into the binding sites of BSA.

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

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

236 y distributed without residual dependence on BSA.

237 optimized operating conditions, the ELP-OPH/BSA/TiO2NFs/c-MWCNTs based biosensor for OPs shows a wid

238 ELP-OPH/BSA/TiO2NFs/c-MWCNTs nanocomposite were systematically c

239 , without any comparable influence of BMI or BSA.

240 No significant BMI-MM or BSA-MM associations were detected when adjusting for hei

241 e C3 convertase stage in comparison with PCh-BSA and PCh-containing Streptococcus pneumoniae cell wal

242 e blood clearance of (13)C-PEG and PEGylated-BSA (bovine serum albumin) following their intravenous i

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

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

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

246 eat-induced BSA nano-aggregates and pristine BSA molecules at room temperature and under physiologica

247 -triazoles and derivatization of the protein BSA with fluorescent dye and polyethylene glycol.

248 urface hydrophobic measurements of proteins (BSA, apomyoglobin, and myoglobin) by these HPsensors dis

249 For two proteins (BSA and a monoclonal antibody), enhanced resolution of t

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

251 0 to 1 mM, there was a decrease in the PVDF-BSA and BSA-BSA electrostatic repulsion forces, resultin

252 forces, which caused a decrease in the PVDF-BSA and BSA-BSA interaction forces accompanied by a decr

253 ymer coated with bovine serum albumin (RAMIP-BSA) was synthesized, characterized and used for direct

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

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

256 etic, and toxicology data rather than simple BSA conversion.

257 A more nonrigid and open structure BSA layer was formed on the membrane surface.

258 By studying BSA adsorption onto carbon nanotubes of increasing radiu

259 the equilibrium constants for the tartrazine-BSA and HSA complexation process were evaluated to be (1

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

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

262 The BSA concentration and the HRP-anti-IgG incubation had ve

263 The BSA-gold nanoclusters/ionic liquid (BSA-AuNCs/IL) was us

264 s of 10 and 100 mM, membrane fouling and the BSA removal rate decreased significantly.

265 60-fold increase in signal strength for the BSA protein with affinity in the nanomolar range.

266 20% to 14.17% in contrast to 18.62% for the BSA-adjusted CKD-EPI and 25.51% for the Cockcroft-Gault

267 e membrane surface, and the structure of the BSA adsorbed layers at corresponding ionic strengths wer

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

269 The effects of glutathione on the BSA conformation were determined using UV-vis spectrosco

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 When the BSA-modified grid was filled with LC and immersed in the

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

274 eraction, as a result of binding of Reb A to BSA, which may ultimately lead to moderation of its tast

275 onfirmed the interaction of this additive to BSA.

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

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

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

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

280 ligomer had a major impact on its binding to BSA.

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

282 en of PBC, 2-octynoic acid (2-OA) coupled to BSA (2OA-BSA) and evaluated the natural history of subse

283 nteractions in the binding of glutathione to BSA and the stabilization of the complex.

284 AVA was normalized to BSA, height, weight, and body mass index.

285 lts have been compared with those related to BSA protein, which does not interact with the used probe

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

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

288 ow that below its CMC, Reb A binds weakly to BSA to generate a Reb A-protein complex ("RPC"), which i

289 Appropriate BSA transformations (BSA(alpha)) were selected for each measurement.

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

291 For the unfolded BSA/curcumin complex, it was found thatp DeltaH(o)F=-16.

292 s for decades, recent recommendations to use BSA to derive interspecies equivalents for therapeutic d

293 ed effects in cultured C2C12 myotubes, using BSA-conjugated palmitate to increase synthesis of endoge

294 nd thus served as biocatalyst for OPs, while BSA was used to stabilize OPH activity in the nanocompos

295 ctrodes, which are subsequently blocked with BSA to avoid unspecific binding.

296 ased proinflammatory responses compared with BSA, regardless of glucose concentrations.

297 ANS interaction with BSA reflects the existence of a large number of binding

298 In multiple regression models, persons with BSA at or above the median (>/=1.86 m(2)) were 2.43 time

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