ライフサイエンスコーパス: buffer solution

1 4 mOmega m(2)) (acetate in a 50 mM phosphate buffer solution).

2 O4 in buffer solution) and SDF (Ag[NH3]2F in buffer solution).

3 5 mm) of ammonium chloride (applied in Hepes-buffered solution).

4 observed in organic solvents or in phosphate buffer solution.

5 e to withstand extensive perturbation of the buffer solution.

6 reshold slope, lower threshold voltage Vt in buffer solution.

7 e specific antigens (PSA) in a physiological buffer solution.

8 d DNA recognition sequences were combined in buffer solution.

9 G) and adenine (A) in physiological pH (7.4) buffer solution.

10 he low solubility of 2,4,6-TBP in an aqueous buffer solution.

11 caine to be introduced over the surface in a buffer solution.

12 ge of the dye compared to that in an aqueous buffer solution.

13 awling as compared to swimming in an aqueous buffer solution.

14 N-hydroxy-l-arginine complex with an aerated buffer solution.

15 monstrated to be highly fluorescent in HEPES buffer solution.

16 mental detection limit of ~300 pM in aqueous buffer solution.

17 ploying sample washing using a pH-controlled buffer solution.

18 4 wks after administering MSCs or phosphate buffer solution.

19 4 wks after administering MSCs or phosphate buffer solution.

20 30 s by Pd-catalyzed deallylation in aqueous buffer solution.

21 e has a linear relationship with the pH of a buffer solution.

22 mer emission in the absence of the target in buffer solution.

23 x molecules in the nucleus than those in the buffer solution.

24 ration of ligand solution, and pH of working buffer solution.

25 ionic liquids were added to a low-conducting buffer solution.

26 ed at a patch-clamp micropipette tip under a buffer solution.

27 emonstrates that Abeta16-22m is monomeric in buffer solution.

28 cavitation between DI water and L-Histidine buffer solution.

29 by the electrochemical approach in phosphate buffer solution.

30 5 nM, and the linear range was 0.5-10 muM in buffer solution.

31 ssy carbon electrode (MWNT/GCE) in phosphate buffer solution.

32 orescent protein (GFP) were first mixed in a buffer solution.

33 converted to 1 in plasma and is stable in a buffer solution.

34 t of PSA with detection limit of 0.5pg/mL in buffer solution.

35 from a solution containing residual DTT to a buffer solution.

36 olymerization and chelates the Mg(2+) in the buffer solution.

37 serum albumin solution than that only in the buffer solution.

38 ally relevant concentrations of oxycodone in buffer solution.

39 ustained water splitting in a pH 7 phosphate buffer solution.

40 trafluoroborate (bminBF4) as electrophoretic buffer solution.

41 3Nf) film modified GCE in a pH 3.5 phosphate buffer solution.

42 lectroanalytical signatures in model aqueous buffer solutions.

43 and ionic measure difference of 0.1 M in non-buffer solutions.

44 mbination with high-purity water and various buffer solutions.

45 he enzyme activity-pH profiles and the pH of buffer solutions.

46 considerable degradation in low- and high-pH buffer solutions.

47 ricted to the introduction of the sample and buffer solutions.

48 lops at the boundaries of the poly-AMPS with buffer solutions.

49 range was simply set by the pH values of the buffer solutions.

50 itro data collected in dilute and controlled buffer solutions.

51 l stimuli, are typically performed in dilute buffer solutions.

52 of the native cytochrome c in physiological buffer solutions.

53 time for protein films prepared from aqueous buffer solutions.

54 fluorescent microsphere particles in aqueous buffer solutions.

55 has an impact on the physical properties of buffer solutions.

56 stability of L-ascorbic acid in aqueous and buffer solutions.

57 ids electrical shorting in conductive (i.e., buffer) solutions.

58 2-AA within 30-60 min in mild acetate-borate buffered solution.

59 age as an electrolyte, thus requiring only a buffered solution.

60 hosphates and oligonucleotides in an aqueous buffered solution.

61 .5 was measured, consistent with a carbonate-buffered solution.

62 entration of cations used in a binding assay buffered solution.

63 ree energy in cells is comparable to that in buffered solution.

64 ity of 0.04 mV.h(-1) is obtained in a pH 8.6 buffered solution.

65 MFI) during freeze-thaw cycling in phosphate buffered solutions.

66 ) and self-decay of ferrate(VI) in phosphate-buffered solutions.

67 e of different photosensitizers dissolved in buffered solutions.

68 state ions formed from these purely aqueous, buffered solutions.

69 om technologically irrelevant single-protein buffered solutions.

70 endent, that is it was not observed in hepes-buffered solutions.

71 prototypes have been shown to work in simple buffered solutions.

72 ompete with other monovalent cations in Tris-buffered solutions.

73 d responses at the low nanomolar level in pH buffered solutions.

74 py recorded images of single MT molecules in buffered solutions.

75 tions, mainly cell culture medium and simple buffered solutions.

76 ent, but are traditionally studied in simple buffered solutions.

77 r the quantification of glucose in phosphate buffer solution (0.25M PBS, pH 7.0), with a linear range

78 aesthetized mice were perfused with a weakly buffered solution (150 mM NaCl + 4 mM Homopipes) at pH v

79 e oxidation of NIC at Britton-Robinson (B-R) buffer solution (4x10(-2)M) of pH range (2.0-8.0) contai

80 net negatively charged liposomes in low-salt buffer solutions, a drop of the apparent pKa from 7.6 to

81 NOESY spectra recorded in 100 and 10% D(2)O buffer solutions allowed the assignment of the nonexchan

82 26 in phosphate buffer solution or phosphate buffer solution alone as a placebo by injection into rig

83 When measured in buffer solution alone, the cyclic voltammetric peaks fro

84 To detect glyphosate in buffer solution, an SPR gold sensor chip is modified by

85 We also modified the pH value of the buffer solution and applied an external electric field t

86 ched zone forms at the interface of the bulk buffer solution and depleted CP zone in the off state or

87 ith limit of detection down to 10 fM in both buffer solution and diluted human serum without pre-puri

88 o 25 muW cm(-2) at 0.5 V potential in simple buffer solution and in cell culturing medium.

89 The influence of pH, type of buffer solution and interfering species possibly present

90 and 17alpha-ethinylestradiol (EE2)from both buffer solution and real wastewater (filtered secondary

91 er cancer cell lines, J-82 and HT-1376, in a buffer solution and spiked urine.

92 immobilized membranes captured S. typhi from buffer solution and this complex was detected colourimet

93 the standard solution of S and N protein in buffer solution and untreated saliva with a detection li

94 e efficient enrichment of rare proteins from buffer solutions and human plasma.

95 Studies in PBS buffer solutions and in a model body liquid demonstrate

96 fication of QD concentration in a variety of buffer solutions and in complex mixtures still remains a

97 tionship between the concentration of MBP in buffer solutions and the impedimetric response was obser

98 red towards the sensing of lactate in model (buffer) solutions and is found to exhibit a linear respo

99 he detection limit of 1 muM of K(+) in clean buffered solution and 30 muM of K(+) in the solution con

100 ure, performed by suspending the sample in a buffered solution and rapidly heating to eliminate endog

101 ed-calcium phosphate (CaCl2.2H2O + K2HPO4 in buffer solution) and SDF (Ag[NH3]2F in buffer solution).

102 bridge filter pad, extracted with an aqueous buffer solution, and analyzed without further sample cle

103 d by electrostatic interactions with salt in buffer solution, and the aggregates displayed enhanced l

104 er surfaces allow SNTs to disperse evenly in buffer solution, and the detection limit of an IgG prote

105 c range of at least 4 orders of magnitude in buffer solution, and the successful detection of c-react

106 ons are present with monovalent cations in a buffer solution, and we found that the thickness of the

107 sed it, effects seen only in CO(2)/HCO(3)(-)-buffered solutions, and blocked by S0859 (cardiac NBC in

108 The buffering solution approach is simpler than the standard

109 ere perfused continuously with weakly Ca(2+)-buffered solutions approximating to the intracellular mi

110 Aqueous buffer solutions are found to help both the oxidative di

111 ein interactions in intact cells rather than buffered solutions are likely more relevant to natural s

112 th aqueous ammonium bicarbonate and pyridine buffer solutions as mobile phases, respectively.

113 ose at 2 fM concentration in a physiological buffer solution at 1 atm O(2) pressure.

114 d DNA, 5'-ATGCTGATGC-3', in sodium phosphate buffer solution at 10 degrees C temperature increments f

115 livers were reperfused with Krebs-Henseleit buffer solution at 37 degree C for 30 minutes.

116 loses a C-terminal fragment when stored in a buffer solution at 4 degrees C.

117 ';6',2''-terpyridine)(2+) (RuPZn) in aqueous buffer solution at a 1:1 stoichiometry.

118 with oxygenated Krebs-Henseleit bicarbonate buffer solution at a pressure of 18 cm H2O in a perfusio

119 the interaction of drug with DNA in acetate buffer solution at pH 4.2 (20% ethanol).

120 range) upon incubation with either phosphate buffer solution at pH 7.4 or in the presence of serum.

121 7 in the presence of NaH(2)PO(4)/Na(2)HPO(4) buffer solution at pH 7.8 achieved chemical ligations, i

122 surements have been carried out in phosphate buffer solution at pH 8.0 in batch mode and low applied

123 tendency to form large aggregates in certain buffer solutions at a concentration range of 10-25 micro

124 Histological sections were incubated in buffer solutions at increasing temperatures (40, 50, 60,

125 re investigated in chloroform and in aqueous buffered solution at a pH of 7.0 and compared to that of

126 ncreased the fluoride release rate in pH 4.0 buffer solution, because of greater surface degradation.

127 In Hepes-buffered solution, both types of neurone responded to ch

128 otein stability is usually studied in simple buffered solutions, but most proteins function inside ce

129 ystem falls between 10 and 10(5) CFU/mL in a buffer solution by cyclic voltammetry (CV) measurements.

130 pin) or both ends (dumbbell) were studied in buffer solution by deep UV femtosecond transient absorpt

131 In phosphate-buffered solution, cis-4-fluoroproline is more active th

132 ow significant degradation in pH 8.4 aqueous buffer solution compared to similarly prepared hydrogels

133 aggregated species is smaller in the acetate buffer solution containing 5% sorbitol than in the aceta

134 were cannulated to perfuse the organ with a buffer solution containing blood vessel stain and methyl

135 tial stripping method (+0.2V (Ag/AgCl)) into buffer solution containing E. coli cells.

136 pared on the PEMC sensor and then exposed to buffer solution containing HSA at 10 microg/mL.

137 hydroquinone (HQ) solution into 40 microL of buffer solution containing hydrogen peroxide.

138 able disulfide or thioether bond, in aqueous buffer solutions containing as little as 5% organic coso

139 theory and simulations show that by using pH buffer solutions containing counter-ions that are beyond

140 quently soaking the crystalline apoenzyme in buffer solutions containing NiCl(2) or ZnCl(2).

141 Aqueous buffer solutions containing pepsin at known constant con

142 sk microelectrodes at the nuclei in isotonic buffer solutions containing redox-active molecules.

143 When measured in buffer solutions containing the holoenzyme or FAD-reduct

144 of the enzyme by adding potassium bromide to buffer solutions containing the wild-type enzyme and by

145 PNA (peptide nucleic acid) beacons, in Tris-buffer solutions containing various concentrations of Na

146 NaCl solution directly into a sodium acetate-buffered solution containing a DOTA (1,4,7,10-tetraazacy

147 cell membrane fragments were suspended in a buffered solution containing bovine serum albumin (BSA)

148 by folding of GGG(TTAGGG)3 single strands in buffered solutions containing Na(+) cations (TEL21/Na(+)

149 a double-stranded DNA oligomer in cacodylate-buffered solutions containing various concentrations of

150 on external calibration in the presence of a buffering solution containing 5 mg L(-1) Na, K, Ca, Mg a

151 n aqueous HbCO samples prepared in different buffers, solutions containing low and high concentration

152 wicking facilitates a gravity-driven flow of buffer solution continuously through paper and nitrocell

153 ses, we assessed whether administration of a buffer solution could improve the immunogenicity of tOPV

154 corresponding free diffusion coefficient in buffered solution (D(f)(34 degrees C)) of 12.6 +/- 0.9 x

155 the formation and shape of the region of the buffer solution depleted of charge carriers (depletion z

156 of the sciatic nerve with the normoglycemic buffer solution did not affect withdrawal thresholds.

157 In a buffer solution, E. coli PI-7 displayed a longer lag pha

158 sphine hydrochloride (TCEP) in the detection buffer solution, each redox molecule on the detection pr

159 uffer and the actual amount present in assay buffer solutions, even at the low concentrations employe

160 When phosphate is in the buffer solution, FMN can bind in either of two ways: by

161 of mannitol, and pre-infusion of an isotonic buffer solution followed by infusion of nanoparticles.

162 measured the current noise in physiological buffer solution for a wide range of different electrode

163 change is detected after exchange into D(2)O buffer solution for any of the pH forms although differe

164 was carried out in NH(4)OAc (0.1 M; pH 5.5)-buffered solution for 30 min at 70 degrees C.

165 re fabricated and immersed in pH 2, 7, or 10 buffer solutions, for 1, 3, 5, 10, 15, and 30 days.

166 or different concentration of human urine in buffer solution (from 1:9 to 4:6).

167 by cholesterol molecule and moves out in the buffer solution, hence, detected electrochemically using

168 The cells were placed in buffer solution in a microfluidic device with electron t

169 l at the both electrodes in Britton-Robinson buffer solution in the range of pH 3.0-12.0, indicating

170 pidly detect thiacloprid and imidacloprid in buffer solutions in a real-time manner.

171 polycrystalline platinum examined in several buffer solutions in a wide range of electrolyte pH from

172 r compositional analysis of buffered and non-buffered solutions in industrial or remote areas.

173 with a stoichiometric balance of reagents in buffered solutions in less than 15 min to give discrete

174 5-E2t-IsoP is significantly more unstable in buffered solutions in vitro and undergoes epimerization

175 found that as the Mg2+ concentration in the buffer solution increased, the diffusion of the ssDNA al

176 re is compromised by mild aging in phosphate-buffered solutions, initiating mesopore collapse.

177 of detection (LOD) for alpha-chymotrypsin in buffer solution is 50 ng/mL, whereas that in chicken bro

178 uefied sputum samples to a culture medium or buffer solution is a critical step because it removes th

179 tion with 200-mM sodium chloride, the former buffer solution is more suitable for conjugate storage.

180 The use of buffer solutions is immensely important in a great varie

181 s, interaction with metal cations in aqueous buffered solution is guided by a breakup of excimers tha

182 ellular environment, in contrast to in vitro buffer solutions, likely imparts similar effects on biom

183 In pH 7.40 phosphate buffer solutions, linear least-squares calibration plots

184 h aggregation propensity of Ascl1 in aqueous buffer solutions make high-resolution studies of this pr

185 of 148, 457 and 309 CFU/mL were obtained in buffer solution, minced beef and tap water samples respe

186 roxides in octanol/H2O and octanol/phosphate buffer solution mixtures were measured to reveal a range

187 omatographic parameters such as column type, buffer solution, mobile phase flow rate and sample injec

188 that of freely dispersed DNA molecules in a buffer solution, MT trajectory could be estimated by sel

189 H-cell reactors with graphite electrodes and buffer solution, NB was reduced stoichiometrically to an

190 In HCO(3)(-)/CO(2)-buffered solutions, no effect of bumetanide on net K(+)

191 ride ion release from disks stored in pH 6.0 buffer solutions occurred mainly by diffusion from disk

192 for both caffeine and paracetamol in acetate buffer solution of pH 4.5 with a correlation coefficient

193 g Fe(III), 1,10-phenantroline, and an acetic buffer solution of pH 5.6.

194 none as electron mediator and 0.1M phosphate buffer solution of pH 6.5.

195 ine (bpy) complex doped in sol-gel matrix in buffer solution of pH 7.3.

196 A buffer solution of phosphate with a pH 4 value was used

197 catalysts in neutral to weakly basic aqueous buffer solutions of CO(2)/HCO(3)(-)/CO(3)(2-) or HPO(4)(

198 on C(18)-bonded Kromasil, equilibrated with buffer solutions of methanol and water (40/60, v/v) cont

199 The rate of the reaction of beta-sultams in buffered solutions of simple primary amines shows a firs

200 Unlike the earlier PTXMAbs, buffered solutions of these conjugates remained homogene

201 erum albumin protein adsorption from aqueous buffer solutions onto gold electrodes functionalized wit

202 bright signal from LC, alpha-chymotrypsin in buffer solution or complex media such as chicken broth c

203 ating the detection of polyphenols either in buffer solution or in real wine samples.

204 x 10(6) MSCs labeled with PKH26 in phosphate buffer solution or phosphate buffer solution alone as a

205 postischemic recovery when administered with buffer solution or plasma alone.

206 functionalized nanoparticles were stable in buffer solution or serum, showing no indication of aggre

207 ce between 1,2-dichloroethane and an aqueous buffer solution or undiluted blood plasma.

208 Increasing the percentage of ethanol in the buffer solution over the range 0-9% increases the inhibi

209 periments were carried out in 0.1M phosphate buffer solution (PBS) at pH 7.0 and 0.1M KCl solution at

210 ied for IMQ determination in 0.1 M phosphate buffer solution (PBS) at pH 7.0.

211 3+), and anionic Fe(CN)6(4-)) in a phosphate buffer solution (PBS) containing AFB1, the magnitude of

212 educed glutathione (GSH) in pH 7.2 phosphate buffer solution (PBS) has been reported.

213 iosensor performance was tested in phosphate buffer solution (PBS) using B394, B131 and B4 biosensors

214 -0.471 V (vs. Ag/AgCl) in a pH 6.5 phosphate buffer solution (PBS).

215 with bovine serum albumin (BSA) in phosphate buffer solution (PBS).

216 l infarction had been treated with phosphate buffer solution (PBS).

217 ent density of 10 mA cm(-2) in 1 m phosphate buffer solution (PBS, pH 7.0).

218 Glucose sensing accomplished in a phosphate buffer solution (PBS, pH=7) for ZnO/MWCNT/GCE samples.

219 electrochemical methods in aqueous phosphate buffer solutions (PBS, pH 7.4).

220 ficiency virus) antibodies (Ab) in phosphate buffered solutions (PBS).

221 ipet) and aspirate (the sink, outer pipet) a buffer solution (perfusate) into each of the two pools.

222 (CurDD) with better chemical stability in a buffer solution pH 7.4.

223 ent solution (pH 12.66 +/- 0.02) and a pH 12 buffer solution (pH 11.92 +/- 0.11).

224 itions, the calibration curve of ketamine at buffer solution (pH 12) exhibits a sensitivity of 8.2 mu

225 y (SWV) scan from -1.2 to -0.3 V in HAc-NaAc buffer solution (pH 4.6) without stripping process was p

226 In acetate buffer solution (pH 5.0), LAC shows a pair of well-defin

227 e oxidation of L-cysteine in 0.1 M phosphate buffer solution (pH 5.0).

228 n the presence of 80 mM pyrrole in phosphate buffer solution (pH 6.0) containing 20mM CEF.

229 rds the oxidations of AT and VC in phosphate buffer solution (pH 7.0) and the corresponding electroch

230 nine dinucleotide (NADH) in a 0.1 M Robinson buffer solution (pH 7.0) using cyclic voltammetry (CV),

231 s to 7.4 atom % N-CNTs in a sodium phosphate buffer solution (pH 7.0) with 2.0 mM NADH (scan rate 10

232 GALOX, at 35 degrees C, using 50mM phosphate buffer solution (pH 7.0).

233 In 0.20 M Tris buffer solution (pH 7.4), an irreversible, overlapping R

234 l measurement of dopamine (DA), in phosphate buffer solution (pH 7.4), with a limit of detection (LOD

235 anode with a Pt counter electrode in aqueous buffer solution (pH = 7), we observe significant photocu

236 of the chosen aromatic in aqueous phosphate buffer solution (pH = 7.3), with the consecutive elimina

237 rom salmon tissue by extraction with citrate buffer solution (pH=4.7) and purified by solid phase ext

238 etection limit reaches to 0.12 nM Con A in a buffer solution (pH=7.4), whereas the addition of nonspe

239 e phosphonate monoalkyl esters are stable in buffer solutions (pH 2.0-7.4) and rabbit serum; furtherm

240 tammetric data for water oxidation in borate buffered solutions (pH 9.2) at electrodes functionalized

241 phate-buffered saline (PBS) (50 mM phosphate buffer solution, pH 7.4, with 150 mM NaCl), higher gluco

242 rapid isolation and detection of E. coli in buffered solution (phosphate buffered saline solution).

243 Administration of a buffer solution prior to vaccination was not associated

244 imulated medium (PSM) and the CAP-stimulated buffered solution (PSB) are able to significantly kill c

245 ct fluorescence burst counts in a variety of buffer solutions regardless of their composition, struct

246 ontrolled by the concentration and pH of the buffer solution, respectively, and (B) a nitroxide radic

247 ests upon irradiation either in hexane or in buffer solution resulted from the well-known Norrish typ

248 Addition of 2-mg/mL chlorhexidine to the buffer solution resulted in the inhibition of specific a

249 Washing the tissue sections in the buffered solution resulted in removal of endogenous solu

250 Characterization of self-assembly in aqueous buffered solutions revealed formation of elongated rod-l

251 successfully applied the GMNC in artificial buffer solution samples and in cancer cell samples, both

252 The effects of lower volumes of buffered solutions should be evaluated further.

253 fcc-FePt NPs pre-etched in the low pH (4.8) buffer solution show nonappreciable cytotoxicity.

254 y charged supramolecular assemblies and free buffer solution show that, even when the amine is proton

255 found in both 1 mM NaHCO3 and 1 mM phosphate-buffered solutions suggested that OH radical was a major

256 with a quantum yield of ~4% in aerated pH 9 buffer solution that drops sharply in deaerated solution

257 0 to 40 ml of filter-sterilized, bicarbonate-buffered solutions that contained 4% dextrose.

258 As T decreases toward Tg of the buffer solution the protein's rotational relaxation time

259 In deareated buffered solutions the open circuit potential of the PdH

260 We also show that in Tris-buffered solutions the Raman signature of supercoiled DN

261 o the case of diluted or molecularly crowded buffer solutions, the G-quadruplex inside the nanocage i

262 In contrast to H2O-buffered solutions, the radius of gyration did not incre

263 In buffered solutions, the travel distance is much shorter

264 arbon Nanotubes (SC-SWCNTs) was added to the buffer solution to improve the resolution.

265 After rinsing with buffer solution to remove the sodium dodecyl sulfate, th

266 ts for normal and perdeuterated bacteria and buffer solutions to distinguish intracellular and transm

267 In aqueous buffer solution, two of the constructs were primarily mo

268 ration did not increase significantly in D2O-buffered solutions up to 55 degrees C, and at 70 degrees

269 omolecule that is attached to the QD and the buffer solution used.

270 In addition, the compound-buffer solutions used in the various biological assays a

271 the native SLPI can be achieved in a simple buffer solution using air oxidation without any suppleme

272 N2O using a 1:1 sodium azide and acetic acid buffer solution using previously established procedures.

273 viscoelasticity) on live fibroblast cells in buffer solutions using Lorentz force excited cantilevers

274 ple membrane and bacteriophage 29 virions in buffer solutions using the phase-contrast images.

275 When bathed in low-pH buffered solutions void of chloride, the porphyrin speci

276 e sensitivity with various concentrations of buffer solution was also investigated in order to determ

277 An extraction procedure using Tris-HCl buffer solution was employed in order to extract water-s

278 Sensor performance in pH 7.0 buffer solution was not reflective of sensor performance

279 EDC coupling in aqueous buffer solutions was also demonstrated using resonance e

280 ns as low as 0.25 wt %, stability in salt or buffer solutions was found to be only achieved at modera

281 ally, for the patients who believed that the buffered solution was less painful, the mean decrease in

282 AL and Li(+), Na(+), K(+), and Cs(+) in Tris buffer solution were determined to be 67+/-42, 120+/-23,

283 2+) in tri-n-propylamide in a pH 7 phosphate buffer solution, where the light generated was collected

284 of Deionized (DI) water and 10mM L-Histidine buffer solution which were subjected to drop shock by ha

285 r, the pH is usually recorded as that of the buffer solution, which can be highly inaccurate.

286 on, the sample solution is replaced with CZE buffer solution while maintaining hydrodynamic flow to e

287 n containing 5% sorbitol than in the acetate buffer solution with 200-mM sodium chloride, the former

288 ible when the guard cells were returned to a buffer solution with an osmotic potential of approximate

289 tion of 2.2 CFU/ml from experimental data in buffer solution with no sample preparation.

290 o 1.3V using CV and DPV methods in phosphate buffer solution with pH 2.0.

291 icular cartilage samples were incubated in a buffer solution with ribose to induce the formation of A

292 duced an amperometric response to glucose in buffer solutions with a sensitivity of 26.4 nA/mM and a

293 he devices exhibit highest sensitivity under buffer solutions with low ion concentration.

294 Reliability tests in different buffer solutions with pH from 4.8 to 9.2 tested over 24

295 cies in a pH-dependent manner in a series of buffer solutions with pH ranges similar to those found i

296 tionalized polystyrene NPs of varied size in buffer solutions with varied ionic strength.

297 quenching by added acetate anion (OAc(-)) in buffered solutions with pH control.

298 range of 30.4 and 243.9 microM in phosphate buffer solution, with a corresponding limit of detection

299 ons ranging from 100-100,000 cells/mL in the buffer solution, with a detection limit of approximately

300 w cost determine histamine concentrations in buffer solutions within pH 7-9.