ライフサイエンスコーパス: buffer solution

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

2 5 mm) of ammonium chloride (applied in Hepes-buffered solution).

3 d DNA recognition sequences were combined in buffer solution.

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

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

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

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

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

9 monstrated to be highly fluorescent in HEPES buffer solution.

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

11 4 wks after administering MSCs or phosphate buffer solution.

12 4 wks after administering MSCs or phosphate buffer solution.

13 30 s by Pd-catalyzed deallylation in aqueous buffer solution.

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

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

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

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

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

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

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

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

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

23 ls of 20, 61, 107, and 142 pS in a 0.5 M KCl buffer solution.

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

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

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

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

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

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

30 by the electrochemical approach in phosphate buffer solution.

31 trafluoroborate (bminBF4) as electrophoretic buffer solution.

32 3Nf) film modified GCE in a pH 3.5 phosphate buffer solution.

33 observed in organic solvents or in phosphate buffer solution.

34 e to withstand extensive perturbation of the buffer solution.

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

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

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

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

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

40 of the native cytochrome c in physiological buffer solutions.

41 time for protein films prepared from aqueous buffer solutions.

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

43 fluorescent microsphere particles in aqueous buffer solutions.

44 can develop at ambient temperature in simple buffer solutions.

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

46 lectroanalytical signatures in model aqueous buffer solutions.

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

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

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

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

51 .5 was measured, consistent with a carbonate-buffered solution.

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

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

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

55 2-AA within 30-60 min in mild acetate-borate buffered solution.

56 e of different photosensitizers dissolved in buffered solutions.

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

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

59 om technologically irrelevant single-protein buffered solutions.

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

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

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

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

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

65 tures in water/trifluoroethanol or phosphate-buffered solutions.

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

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

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

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

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

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

72 26 in phosphate buffer solution or phosphate buffer solution alone as a placebo by injection into rig

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 roducts of Ru(bpy)3(2+) in water, in aqueous buffered solutions and encapsulated in zeolite-Y have be

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

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

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

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

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

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

95 ts to a greater extent than acidic phosphate buffer solution, applied at a similar pH to the same aff

96 The buffering solution approach is simpler than the standard

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

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

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

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

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

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

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

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

105 ';6',2''-terpyridine)(2+) (RuPZn) in aqueous buffer solution at a 1:1 stoichiometry.

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

107 gly reduced form, BV*+, in a pH 7.4 Tris-HCl buffer solution at mu = 8.4 mM.

108 itrite (OONO(-)) in aqueous sodium phosphate buffer solution at neutral pH was investigated.

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

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

111 h in the cells when they are stored in a PBS buffer solution at pH 7.4.

112 7 in the presence of NaH(2)PO(4)/Na(2)HPO(4) buffer solution at pH 7.8 achieved chemical ligations, i

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

114 he ferriheme protein metmyoglobin (metMb) in buffer solution at physiological pH 7.4 reversibly binds

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

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

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

118 only CuA, were recorded in both H2O- and D2O-buffered solution at pH 7.5.

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

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

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

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

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

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

125 f 5 bp were obtained in 5 mM pH 7.1 Tris-HCl buffer solution containing 50 mM NaCl.

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

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

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

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

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

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

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

133 Aqueous buffer solutions containing pepsin at known constant con

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

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

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

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

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

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

140 teinated enamel samples were equilibrated in buffered solutions containing 10(-5) to 10(-3) mol/L flu

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

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

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

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

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

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

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

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

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

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

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

152 ted MPS and functional peptide in an aqueous buffered solution, eliminating the need for additional c

153 The internal buffer solution ensures independence of sample condition

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

155 ed alkaline OONO(-) solution were added to a buffer solution (final pH 7.0-7.2), and the formation of

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

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

158 e aged subgroup was immersed in an inorganic buffer solution for 2 wks before being thermocycled.

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

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

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

162 res that do not form fibers in physiological-buffered solution for up to 8 h of continuous imaging.

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

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

165 as induced by superfusion with a bicarbonate-buffered solution gassed with a progressively increasing

166 acidified by superfusion with a bicarbonate-buffered solution gassed with increasing concentrations

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

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

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

172 5-E2t-IsoP is significantly more unstable in buffered solutions in vitro and undergoes epimerization

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

174 tive and mutant N2OR spectra recorded in H2O-buffered solutions indicated that several additional sig

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

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

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

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

179 ic conversion at room temperature in aqueous buffer solution is unlikely.

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

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

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

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

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

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

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

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

190 superoxide ion radicals even in a cell-free buffer solution of AA, but not in that of BHB.

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

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

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

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

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

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

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

198 ion of allyl amine and vinyl acetic acid) in buffered solutions of neutral pH.

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 ative humidity and surface pretreatment with buffer solutions on the ionic conductivity of a mica sur

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

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

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

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

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

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

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

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

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

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

215 -0.471 V (vs. Ag/AgCl) in a pH 6.5 phosphate buffer solution (PBS).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

231 GCGTT) dissolved in air-equilibrated aqueous buffer solution (pH 7.5).

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

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

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

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

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

237 nts after 20-s incubation in D(2)O phosphate-buffered solution (pH 5.7).

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

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

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

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

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

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

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

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

246 CD measurements for calmodulin in buffered solution revealed that its alpha-helical conten

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

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

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

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

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

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

253 e addition of the surfactant Tween 80 to the buffer solution that is used in forming the antibody-ant

254 0 to 40 ml of filter-sterilized, bicarbonate-buffered solutions that contained 4% dextrose.

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

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

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

258 ity of the detergent micelles to that of the buffer solution, the micelle contribution to the small a

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

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

261 In buffered solutions, the travel distance is much shorter

262 ntails (1) ultrasonication in basic ammonium buffer solution to extract CrVI from environmental matri

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

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

265 paper blotter saturated with a 45Ca-labeled buffer solution to the mucosal surfaces of slit-open emb

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

267 Using chelate buffered solutions to quantify Zn(2+) influx in the nano

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

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

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

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

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

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

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

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

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

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

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

279 In the optimized LLE method, a formate buffer solution was first loaded into a 96-well filter p

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

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

282 from 2,027 to 23,130 bp in Tris-borate-EDTA buffer solutions was investigated.

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

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

285 nd regardless of whether Hepes- or HCO3-/CO2-buffered solutions were used.

286 2+) in tri-n-propylamide in a pH 7 phosphate buffer solution, where the light generated was collected

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

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

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

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

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

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

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

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

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.