ライフサイエンスコーパス: mM

1 lly enriched (57)Fe(II) solution (0.1 or 1.0 mM Fe(II)) at pH 5.5 and 7.

2 n of 254 differentially expressed genes at 0 mM NaCl and 391 genes at 300 mM NaCl in P. indica-coloni

3 PBS, pH 7.0), with a linear range between 0 mM and 0.9mM, high sensitivity and selectivity, and a lo

4 etection limit of 0.1-8 mM and 0.05 +/- 0.01 mM, respectively.

5 ose concentration decreased by 0.27 +/- 0.05 mM (p < 0.001).

6 e A concentration in the range of 0.001-0.05 mM (R(2)=0.8308) and 0.075-1.25 mM (R(2)=0.9920) with a

7 hed as low as 0.060 mM for glucose and 0.059 mM for lactate, based on a 20-muL conditioned microdialy

8 NIR absorption, high relaxivity (r 1 = 14.06 mM(-1) s(-1) ), low risk of release of Gd ions, and NIR-

9 m's detection limits reached as low as 0.060 mM for glucose and 0.059 mM for lactate, based on a 20-m

10 enzyme kinetics provided similar Vmax (0.079 mM/min) and Km (0.36 mM) values as those found in the li

11 1 +/- 0.13 mAcm(-2) with a KM of 1.6 +/- 0.1 mM and a sensitivity of 400 +/- 20 muAcm(-2)mM(-1) while

12 ty of the actin filaments at [MgATP] </= 0.1 mM and local bending of the filament front upon each myo

13 From solutions with 0-0.1 mM Cr(III), the particles on quartz grew from 2 to 4 nm

14 Experimental conditions (i.e., 0.1 mM Mn(2+) (aq) concentration and pH 10.1) were chosen to

15 itol (11 muM) and galactose 1-phosphate (0.1 mM), (corresponding to plasma concentrations in patients

16 then aggregates in a downhill fashion at 0.1 mM.

17 2 min) within the detection range of 0.04-1 mM.

18 CME (IC50(CME) = 65.9 +/- 7.7 to 3.7 +/- 1.1 mM), which makes this series among the more potent inhib

19 age faster than the 2-6, and a KM of 2 +/- 1 mM (Vmax, 400 +/- 100 muM/min) was obtained for the 6'-s

20 ed acid plus conjugate base) of 257 and 27.1 mM, respectively.

21 ch displays a dissociation constant Kd = 3.1 mM suitable for the detection of low millimolar concentr

22 , 3 mM tetraethylammonium, 1 mM ZnCl2, and 1 mM CuSO4.

23 atom exchange in experiments with 0.1 and 1 mM Fe(II), respectively.

24 emonstrated that mixing the analog 1728 at 1 mM with sucrose almost completely inhibited the detectio

25 ter permeability of SjAQP was inhibited by 1 mM HgCl2, 3 mM tetraethylammonium, 1 mM ZnCl2, and 1 mM

26 in human nuclei in situ was stabilized by 1 mM MgCl2, but became disrupted in the absence of MgCl2,

27 eral incubation with a high concentration (1 mM) of conjugated bile acids.

28 ce of resting levels of free [Mg(2+)]cyto (1 mM).

29 ort for an energy-sensing attribute (i.e., 1 mM Km for ATP) of the 5-InsP7-generating inositol hexaki

30 In the whole cohort, each 1 mM (18 mg/dL) increase in mean FBG and RBG and each 1% i

31 -10 was reused as the PKM2 immunoblot from 1 mM Glu, fractions 1-10.

32 Increasing ionic strength from 1 mM to 100 mM sodium chloride significantly reduced or co

33 2HG concentration > 1 mM could be reliably detected with high confidence.

34 ed RNA synthesis at near physiological (>/=1 mM) Mg(2+) concentrations, enabling templated RNA synthe

35 rage on the quartz substrate than those in 1 mM and 10 mM IS systems.

36 that follows prolonged CaCC activation in 1 mM Ca(2+).

37 109% (95% CI, 3-323%; P = 0.041) increases/1 mM, respectively).

38 Inosine (1 mM) delivered intravesically to SCI rats during consciou

39 In isolated tissue assays, inosine (1 mM) significantly decreased the amplitude of spontaneous

40 and low carbon substrate concentrations (<1 mM fructose) into site wells.

41 the excitatory amino acid glutamate (10 nM-1 mM) elicited reproducible and reversible transient incre

42 -1284 bound to M1 mAChR in the presence of 1 mM ACh with Kd, 4.23 nM, and saturable binding capacity

43 nites (NAu-1 and NAu-2) in the presence of 1 mM aqueous Fe(II) at pH 7.8.

44 Addition of 1 mM ATP substantially reduces the light scattering of sol

45 0 mum above its surface in the presence of 1 mM glucose and artificial saliva solution (pH 7.2 at 37

46 le of measuring potassium, in the range of 1 mM to 100 mM, with high sensitivity and selectivity, by

47 At an external calcium concentration of 1 mM, and a membrane potential of -20 mV, we found that th

48 rly soluble in urine with a solubility of ~1 mM and can readily form microcrystals that lead to cysti

49 w N (5 mM and 0.4 mM, respectively) and P (1 mM and 2 muM, respectively) supply in 37 species from si

50 ed by 1 mM HgCl2, 3 mM tetraethylammonium, 1 mM ZnCl2, and 1 mM CuSO4.

51 ays post-fertilization zebrafish larvae to 1 mM ACR for 3 days.

52 etected in synthetic urine samples down to 1 mM using merely a 188 MHz NMR spectrometer.

53 o modify the ionic strength from 500 mM to 1 mM, causing a reversible reduction in the fluorescence q

54 oncentration in the sample from 0.1 muM to 1 mM, scan rate from 25 mV s(-1) to 200 mV s(-1), and angu

55 Equilibrating NOM with 1 mM Ca(2+) in dose-limited systems prior to dosing with F

56 Binding is optimal with 1 mM MgCl2 but decreases with both lower and higher magnes

57 lysis, detect glucose accurately in the 1-10 mM range.

58 mns at pH 7.9 (10 mM HCO3(-)) and pH 3.4 (10 mM CH3COOH) to evaluate the effect of environmentally re

59 eacted in flow-through columns at pH 7.9 (10 mM HCO3(-)) and pH 3.4 (10 mM CH3COOH) to evaluate the e

60 At concentrations above 10 mM NaCl, pitting is initiated at the outer rim of the co

61 egraded substantially in 1:1 acetonitrile:10 mM PBS, pH 7.4, at 37 degrees C, generating primarily o(

62 yeast wild-type strain with 10 mM SSA and 10 mM GHB didn't affect the growth.

63 e quartz substrate than those in 1 mM and 10 mM IS systems.

64 es to different concentrations (1, 3, and 10 mM) of bicarbonate (HCO3(-)) under light and dark condit

65 aturated with Na(+) (100 mM), K(+) (1 and 10 mM), NH4(+) (10 mM) or Ca(2+) (5 mM) revealed a high ads

66 d into dimethylsulfoxide (DMSO) group and 10 mM, 15 mM, and 20 mM A-803467 groups.

67 rge excess of Cl(-) ([I(-)] approximately 10 mM and [Cl(-)] approximately 3.7 M), I(-) is oxidized in

68 m completely degraded up to approximately 10 mM SCN(-) to ammonium and sulfate, with some evidence of

69 t the shear induced Ca(2+) influx, but at 10 mM it produced significant inhibition.

70 ter rim of the confined zone, while below 10 mM NaCl, pitting is initiated inside the confined zone.

71 xocytosis by the slow Ca(2+) buffer EGTA (10 mM) in basal hair cells tuned to high frequencies ( appr

72 trocumene; donor, 1 muL of basic drugs in 10 mM HCl; and extraction potential, 250 V), experimentally

73 (+) (100 mM), K(+) (1 and 10 mM), NH4(+) (10 mM) or Ca(2+) (5 mM) revealed a high adsorption affinity

74 The combination of nitrate (10 mM) and Fe(II) (4 mM), resulted in mineral precipitation

75 hese effects were reversed by addition of 10 mM 2,3-butanedione 2-monoxime.

76 pyruvate were produced in the presence of 10 mM cysteine, indicating that cysteine is actively catabo

77 Randles-Sevcik analysis of 10 mM K3[Fe(CN)6] in 0.1 M KCl using the electrode chip gav

78 When lactate again reached 10 mM after LVR, full resuscitation was started with crysta

79 ium acetate following 24-hour exposure to 10 mM ammonium acetate were complemented by in vivo studies

80 but only Npas1 neurons were sensitive to 10 mM ethanol.

81 A concentration was increased from 0.3 to 10 mM, formation of additional products was observed with M

82 t the onset from fresh to brackish water (10 mM, or 0.06% salinity) to 0.52% in ocean water salt conc

83 Treatment of yeast wild-type strain with 10 mM SSA and 10 mM GHB didn't affect the growth.

84 iors across a range of ionic strength (1-100 mM) and pH (2-9.5) conditions.

85 centrations in the membrane are high (10-100 mM), however, and there is no experimental evidence ruli

86 0 mM, 2.3 wt%) and dilute sulfuric acid (100 mM, 1.0 wt%) at 120 degrees C for 5 min removed 85.7% of

87 t was stable in both 20% mouse serum and 100 mM EDTA, whereas the nickel-conjugated trimers were not

88 raction solutions of deionized water and 100 mM NH4OH), more than 99.3% NaCl was removed from samples

89 free anion in the extracellular space (>100 mM) and within the cytoplasm in eukaryotes (10 approxima

90 In 100 mM IS system, nucleated Mn (hydr)oxide particles had mor

91 ific antigen (PSA) from 1 to 1,000 nM in 100 mM phosphate buffer.

92 m 4 to 400 mg/dL or 0.10-10.34 mmol/L in 100 mM phosphate-buffered saline (PBS) without significant i

93 utral pH on illite saturated with Na(+) (100 mM), K(+) (1 and 10 mM), NH4(+) (10 mM) or Ca(2+) (5 mM)

94 amate antagonist, kynurenic acid (50 nl; 100 mM) into RVLM, blocked the seizure-induced 43.2 +/- 12.6

95 length of 1 mm, we were able to suppress 100 mM hydroxide @ 100 nL/min (10 neq/min).

96 Increasing ionic strength from 1 mM to 100 mM sodium chloride significantly reduced or completely s

97 tate detection in the range from 3 mM to 100 mM with the detection limit of 1.5 mM; response time is

98 uring potassium, in the range of 1 mM to 100 mM, with high sensitivity and selectivity, by ISPAO base

99 uivalent antioxidant capacity of 135 and 108 mM Troloxmg(-1) extract, respectively.

100 0.163 mM for creatinine deaminase and 0.139 mM for urease, respectively.

101 lectrocatalytic amplification provided by 15 mM hydrazine in 5 mM phosphate buffer (PB; pH 7) over 10

102 dimethylsulfoxide (DMSO) group and 10 mM, 15 mM, and 20 mM A-803467 groups.

103 ine, followed by the addition of sucrose (15 mM) after 0, 6, 20, or 48 h.

104 complex ions are formed directly from a 150 mM KCl and 25 mM Tris-HCl buffer at pH 7 that is widely

105 oncentrations of the target analytes and 150 mM of NaCl.

106 through PA imaging) to the intracellular 150 mM typical values (through fluorescence imaging).

107 Ethanol up to 150 mM did not affect tight junction integrity or barrier fu

108 ed by instruments in the range of 0.5 to 150 mM.

109 recovery (FRR) during BW at 8 V AC using 155 mM NaCl.

110 tinine and urea calibration curves, of 0.163 mM for creatinine deaminase and 0.139 mM for urease, res

111 gical-like conditions of ionic strength (163 mM) in 50 mM Tris-HCl (pH 7.4) at 37 degrees C.

112 cally relevant concentrations of ethanol (17 mM; 0.1% v/v).

113 mopentamers were 6 +/- 1, 40 +/- 11, and >18 mM, respectively), whereas GABAAR-null cells were unresp

114 chieved with an initial concentration of 0.2 mM ascorbic acid.

115 which provided similar sensitivity (ca. 0.2 mM(-1)) when normalized to the same standard.

116 Subsequent treatment (0.2 mM) with acid (Yb(OTf)3, CH3CN, 80 degrees C) promotes a

117 n constant for ammonium in N. maritimus (0.2 mM), which is orders of magnitudes higher than previousl

118 stimulated by NO2(-) at levels as low as 0.2 mM.

119 rtex, in physiological external calcium (1-2 mM).

120 In the range of 0.05-1.2 mM ascorbic acid, maximum levels of measurable hydrogen

121 DNAN was degraded by 1.2 mM Fe(II) at pH 7, 8, and 9, and rates increased with in

122 s recombinant Drp1 GTPase activity (Ki > 1.2 mM).

123 ith strong pi affinity nullified (IC50 = 2.2 mM) the responsiveness of anion-pi catalysts to electric

124 cid linkages generated a KM value of 3 +/- 2 mM (Vmax, 900 +/- 300 muM/min) for 3'-sialyllactose.

125 4 displays positive chemotaxis towards 0.5-2 mM As(III).

126 Gola di Lago, Switzerland) with sulfide (5.2 mM, S(-II)spike/Fe = 0.75-1.62 mol/mol) at neutral pH an

127 Extracellular Mg(2+) at 2 mM did not significantly affect the shear induced Ca(2+)

128 imately 0.04 pA, increasing to 0.065 pA at 2 mM external calcium, and 0.12 pA at 5 mM.

129 was larger at lower ionic strength (e.g., 2 mM).

130 leration for several low concentra- tion (<2 mM) metabolites.

131 In the presence of 1 or 2 mM Fe(II), under anoxic conditions, U(VI) uptake by the

132 lso observed with 5 mM NO3(-) for 1 day or 2 mM NO3(-) for 3 days.

133 r response (20 nM to 20 muM and 100 muM to 2 mM), low detection limit (2.0 nM), and good selectivity

134 eve high sensitivity (2.4 +/- 0.24 mA cm(-2) mM(-1)) for H2O2 oxidation.

135 es, with good sensitivity (- 0.27microAcm(-2)mM(-1)), low limit of detection (126microM) and long lin

136 M and a sensitivity of 27.5+/-2.5microAcm(-2)mM(-1).

137 (26.9muM) and good sensitivity (3.5muAcm(-2)mM(-1)).

138 l amperometry were 112.37 and 282.82muAcm(-2)mM(-1) respectively, and the corresponding limits of det

139 mM and a sensitivity of 400 +/- 20 muAcm(-2)mM(-1) while operating with an applied potential of 0.3

140 foxide (DMSO) group and 10 mM, 15 mM, and 20 mM A-803467 groups.

141 High concentrations of Fe(2+) (10 and 20 mM) rapidly (<10 min) transformed jarosite to a green ru

142 amined in HepaRG cells treated with APAP (20 mM).

143 cytoplasm in eukaryotes (10 approximately 20 mM).

144 2+) that is much less substantial than at 20 mM K(+) (-120 mV vs -210 mV).

145 give a potential near the DNA surface at 20 mM Mg(2+) that is much less substantial than at 20 mM K(

146 ive when lower concentrations of calcium (20 mM) and phosphate were used.

147 icating concentrations of ethanol, i.e., >20 mM, each activate GIRK2 channels directly, in the absenc

148 An excess supply of 20 mM Pi (P20) produces a shallow root system architecture

149 s improved by 29 times in the presence of 20 mM sulfite.

150 e-based potassium sensing in the range of 20 mM to 1 M.

151 66 Hz/mM.cm(2) and a linear range of 1 to 20 mM.

152 o changes in glucose concentration (2 vs. 20 mM).

153 s incubated with medium supplemented with 20 mM fructose than in hepatocytes incubated with medium su

154 ation at higher reagent levels (Ca(2+) = 200 mM), as also seen with peptide-silk chimeric materials,

155 A/m(2), R(2) = 0.97) and then from 30 to 200 mM (8.50 to 10.80 mA/m(2), R(2) = 0.95).

156 broad linear response range of 5 muM to 200 mM with a near Nernstian slope of 28 mV/log[a(Ca(2+))].

157 macrocyclization at concentrations up to 200 mM.

158 th trypsin, the digests were eluted with 200 mM ammonium bicarbonate at pH 8.2 for CZE-MS/MS analysis

159 Michaelis constant Km and Imax equal to 0.24 mM and 0.13 mA cm(-1), respectively.

160 enhanced T1 relaxivity (r1 approximately 24 mM(-1)s(-1)) even at 4.7 T, substantially surpassing con

161 diastolic [Ca] nadir to 200 nM (at Pup = 24 mM/s).

162 Interestingly, from solution with 0.25 mM Cr(III), particles of two distinct sizes (2 and 6 nm)

163 f 0.001-0.05 mM (R(2)=0.8308) and 0.075-1.25 mM (R(2)=0.9920) with a detection limit (S/N=3) of 0.264

164 are formed directly from a 150 mM KCl and 25 mM Tris-HCl buffer at pH 7 that is widely used in protei

165 lysis was higher in explants incubated in 25 mM glucose (HG) for 24 h compared to controls (C: 5.5 mM

166 cal mu-EME conditions (acceptor, 1 muL of 25 mM HCl; FLM, 1 muL of 4-nitrocumene; donor, 1 muL of bas

167 atch mode), at a glucose concentration of 27 mM.

168 culture media, or media supplemented with 28 mM glucose, 200 muM palmitic acid, and 200 muM oleic aci

169 rve river (12.3 +/- 0.2 muM and 22.5 +/- 0.3 mM carbonate and bicarbonate, respectively).

170 nactivation of E. coli was achieved with 0.3 mM H2O2 or PDS at 5.2 x 10(-5) Einstein.L(-1) photo flue

171 As a positive control, 0.3 mM HgCl2 inhibited AQP1 water permeability by >95%.

172 In contrast, 0.3 mM SSA has severely affected the growth of plants.

173 his study, we show that while high C2H2 (1.3 mM) concentrations reversibly inhibit reductive dechlori

174 alpha 3 = 1.03 +/- 0.01, and C 1 = 23 +/- 3 mM, which are comparable to the expected physiological v

175 ted in a release of 2.8 mM galactose and 4.3 mM N-acetylneuraminic acid; these sugar concentrations w

176 Gd(III) chelating agents (r1 approximately 3 mM(-1)s(-1) at 4.7 T) currently in clinical use.

177 allows lactate detection in the range from 3 mM to 100 mM with the detection limit of 1.5 mM; respons

178 lity of SjAQP was inhibited by 1 mM HgCl2, 3 mM tetraethylammonium, 1 mM ZnCl2, and 1 mM CuSO4.

179 es incubated with medium supplemented with 3 mM fructose.

180 cm(-2) and a detection limit of 1.1 x 10(-3) mM.

181 estimated as 0.193mM, 8.170muA, 7.035x10(-3)mM and 65.816muA/mMcm(2), respectively.

182 and [Formula: see text] approximately 10-30 mM.

183 e (GA), or activation of this reaction by 30 mM HPO3(2-).

184 sion upon presentation of a sour tastant (30 mM citric acid).

185 rated by stimulation with a sour tastant, 30 mM citric acid.

186 urrent densities and VFA levels from 1 to 30 mM (0.04 to 8.50 mA/m(2), R(2) = 0.97) and then from 30

187 linear calibration range from 1.7 muM to 30 mM for the determination of H2O2 with a low limit of det

188 eased up to 0.9 Hz after stimulation with 30 mM KCl in cultured cells.

189 nt of yellow poplar with peracetic acid (300 mM, 2.3 wt%) and dilute sulfuric acid (100 mM, 1.0 wt%)

190 ssed genes at 0 mM NaCl and 391 genes at 300 mM NaCl in P. indica-colonized compared to non-inoculate

191 of 0.08% (w/v) ethanol (IC50 = 0.2% v/v, 34 mM).

192 se analyte, a linear dynamic range of 0.5-35 mM glucose is observed.

193 ded similar Vmax (0.079 mM/min) and Km (0.36 mM) values as those found in the literature.

194 9 +/- 0.59 mM, absolute error: 0.46 +/- 0.39 mM).

195 with the experimental linearity in 0.04-0.4 mM range and having the limit of detection (LOD) value o

196 ous competing electron acceptors and 0.3-0.4 mM trichloroethene, trichloroethene removal was sustaine

197 es containing D. mccartyi sp., low C2H2 (0.4 mM) concentrations do not inhibit growth or metabolism o

198 tes at -15 degrees C in the presence of (0.4 mM) NaBAr(F)4 as compared with a very slow reaction at 1

199 dy assessed how high and low N (5 mM and 0.4 mM, respectively) and P (1 mM and 2 muM, respectively) s

200 .7 mM ([Ca(2+)] in artificial saliva) to 1.4 mM at 20 mum above the surface.

201 combination of nitrate (10 mM) and Fe(II) (4 mM), resulted in mineral precipitation and rapidly decre

202 Knoevenagel condensation ( approximately 40 mM, rt, CH2Cl2, piperidine/AcOH/molecular sieves) of a d

203 higher eluent concentrations (at least to 40 mM carbonate), paving the way for future higher capacity

204 The addition of NaCl (300-400 mM) only caused flocculation in nanodispersion stabilize

205 8 muL samples of both hydrogen peroxide (0-5 mM, 2.72 x 10(-6) A.mM(-1)) and total cholesterol in ser

206 only used perchloric acid, combined with 0.5 mM ascorbic acid prevents significant oxidation of the a

207 best catalyst-substrate combinations at 0.5 mM catalyst concentration are 3.6 x 10(5)-fold for HPNP,

208 Nicotine alone </=0.5 mM had little to no effect in any of these assays.

209 no nitrogen or with low nitrogen (i.e., 0.5 mM KNO3).

210 assiduously maintained at approximately 0.5 mM through a combination of dietary uptake, de novo synt

211 ver, an increase of free [Mg(2+)]cyto to 1.5 mM could increase the period between Ca(2+) waves.

212 GHB concentrations up to 1.5 mM didn't affect shoots of Arabidopsis plants; however,

213 luminal Ca(2+) was increased from 0.1 to 1.5 mM.

214 mM to 100 mM with the detection limit of 1.5 mM; response time is 2-3 min.

215 unded between 9 mM at resting state and 11.5 mM; and 3) the cells can maintain [Na(+)]sm to the above

216 ) (1 and 10 mM), NH4(+) (10 mM) or Ca(2+) (5 mM) revealed a high adsorption affinity of Tl(+) in Na(+

217 crotic cell death pathway activation and 2.5 mM compound 1 also prevented the loss of mitochondrial m

218 epetitive stimulation in the presence of 2.5 mM extracellular Ca(2+), compared to muscles from contro

219 Gaspe Flint maize plants grown in 0.5 or 2.5 mM NO3 (-) throughout the lifecycle.

220 The optimal method employed 2.5 mM TSPP used in a 1:100 (m/v) soil-to-reagent ratio, wit

221 (1.9-2.2 mum) and external [Ca(2+)]o (1-2.5 mM), which produce an increase of TP, do not affect the

222 upper limit for the solution affinity at 2.5 mM.

223 own in vitro under either 2.5 (H2O2L) or 3.5 mM H2O2 (H2O2H).

224 Different sulfate pre-treatments (0, 0.5, 5 mM, 3 d) were also tested for effects on selenate uptake

225 e (HG) for 24 h compared to controls (C: 5.5 mM glucose).

226 ectrodes was linear from 2.5 x 10(-3) to 6.5 mM with a sensitivity of 191.6 muA mM(-1)cm(-2) and a de

227 a4betadelta current, reduced activity in 8.5 mM K(+) at puberty, while blockade of alpha5-GABARs had

228 ast, lower concentrations of Fe(2+) (1 and 5 mM) led to the formation of lepidocrocite.

229 ularly applied ammonium chloride as low as 5 mM causes intracellular Ca(2+)-increase and a reduction

230 A at 2 mM external calcium, and 0.12 pA at 5 mM.

231 (+) concentrations, from the extracellular 5 mM typical values (through PA imaging) to the intracellu

232 The PKM2 immunoblot from 5 mM Glu, fractions 1-10 was reused as the PKM2 immunoblot

233 Long PEGs at higher ionic strengths (>/=5 mM) caused particle loss due to bridging adsorption at t

234 r density of 275 muW cm(-2) is obtained in 5 mM glucose in PBS, the highest to date under these condi

235 plification provided by 15 mM hydrazine in 5 mM phosphate buffer (PB; pH 7) over 100 to 300 s.

236 t loss mechanism at low ionic strengths </=5 mM for any of the studied particles.

237 Our study assessed how high and low N (5 mM and 0.4 mM, respectively) and P (1 mM and 2 muM, resp

238 +/- 1.6% of DDE were degraded by sulfide (5 mM) in the presence of graphite powder (21 g/L) after 28

239 A change in the chloride level up to 5 mM had a negligibly effect on the reaction kinetics.

240 h salt, from [Formula: see text]5 pN under 5 mM ionic strength to near zero at 1 M.

241 he maximum recovery rate was observed with 5 mM NO3(-) added for 3 days; however, slower but signific

242 ignificant recovery was also observed with 5 mM NO3(-) for 1 day or 2 mM NO3(-) for 3 days.

243 as obtained within concentrations of 0.03-50 mM with a response time of approximately 3 s.

244 was found to be most sensitive to Sr(2+) (50 mM shifted G(V) by +21.7 mV), and Kv2.1 to be the least

245 e) with standard solutions in formic acid 50 mM.

246 observed that buffer (pH 6.7) containing 50 mM tris-base appears to be excellent extractant as activ

247 ther show that acute exposure of ethanol (50 mM) to striatal slices activates delta opioid receptors

248 ) M(-1) for CB7 and CB8, respectively, in 50 mM sodium acetate-d3 D2O solution (pD 4.7).

249 conditions of ionic strength (163 mM) in 50 mM Tris-HCl (pH 7.4) at 37 degrees C.

250 The often-used 50 mM ammonium chloride causes more extensive and persisten

251 ter topical exposure to vasoconstrictors (50 mM KCl and 20 nM Endothelin-1).

252 nvironments (20-50 degrees C, 2-10 pH, 0-500 mM NaCl, and 0-35 days storage at 25 degrees C) depended

253 .52% in ocean water salt concentrations (500 mM, or ~0.3% salinity).

254 of 319.8 mM of itaconate (41.6 g/L) from 500 mM citrate without any buffer system or additional cofac

255 e used to modify the ionic strength from 500 mM to 1 mM, causing a reversible reduction in the fluore

256 100% of gaseous CO2 to formic acid, and >500 mM formate was observed to accumulate in solution.

257 uid, with resolution and sensitivity (1.51nA/mM) comparable to that of state-of-art commercial CGM sy

258 id conditions (pH 6-9, ionic strength 10-550 mM) had no influence on transfer as shown for MS2.

259 samples was promising (error: -0.09 +/- 0.59 mM, absolute error: 0.46 +/- 0.39 mM).

260 sensor demonstrated a sensitivity of 12.5muA/mM (determined according to the drain current difference

261 confocal microscope after immersion in a 0.6 mM solution of acridine orange dye for 10-20 seconds.

262 to be relatively high (Kd approximately 1.6 mM) compared with other monovalent cations and relevant,

263 eration at which 80% of the supplied H2S (61 mM d(-1)) was biologically oxidized to elemental sulfur.

264 were observed at concentrations between 4-64 mM, and were not dependent on the increase in intracellu

265 rease the calcium ion concentration from 0.7 mM ([Ca(2+)] in artificial saliva) to 1.4 mM at 20 mum a

266 r 1 and r 2 relaxivities of 223.8 and 344.7 mM(-1 )s(-1) (1.5 T), respectively.

267 actant-saturated complexes above 5.6 and 4.7 mM RL, respectively, leaving the remaining RL in free mi

268 the fronds of PV grown in 0.67, 3.3 and 6.7 mM AsV.

269 0 nM and a broad linear range of 250 nM to 7 mM.

270 edented combination of high solubility (>700 mM in CH3CN), multiple electron transfers at low redox p

271 enging activity (53.3%) and FRAP value (3.71 mM)), whereas pH 6.5 with the same extraction time, S/E

272 ing electrolysis of wastewater containing 75 mM Cl(-).

273 pH dynamics by pretreating biofilms with 75 mM arginine, followed by the addition of sucrose (15 mM)

274 formed from which Km values of 0.29 and 0.79 mM were derived, respectively.

275 A KM value of 3.3 +/- 0.8 mM (Vmax, 2100 +/- 200 muM/min) was obtained for 3'-sial

276 ly diminished at ascorbic acid levels of 0.8 mM or above.

277 response range and detection limit of 0.1-8 mM and 0.05 +/- 0.01 mM, respectively.

278 NanA to the FBS resulted in a release of 2.8 mM galactose and 4.3 mM N-acetylneuraminic acid; these s

279 .7% of the influent trichloroethene (1.5-2.8 mM) and produced ethene as the main product.

280 ere able to catalyze the conversion of 319.8 mM of itaconate (41.6 g/L) from 500 mM citrate without a

281 sialic acid species formed in vitro was 97.8 mM/sec at 1.5 T and 298 K.

282 ctivities (i.e., ABTS (42.2%) and FRAP (0.81 mM)) and alpha-amylase inhibitory activity (62.1%), was

283 ining the [Na(+)]sm value to approximately 9 mM; 2) at 2 Hz pacing frequency, [Na(+)]sm is bounded be

284 Hz, the upper and lower bounds converge at 9 mM, constraining the [Na(+)]sm value to approximately 9

285 ng frequency, [Na(+)]sm is bounded between 9 mM at resting state and 11.5 mM; and 3) the cells can ma

286 ) and total cholesterol in serum from 0 to 9 mM (1.34 x 10(-8) A.mM(-1), r(2) = 0.99, RSD < 10%, n =

287 s over a wide range of potencies (15 pM to 9 mM).

288 h hydrogen peroxide (0-5 mM, 2.72 x 10(-6) A.mM(-1)) and total cholesterol in serum from 0 to 9 mM (1

289 rol in serum from 0 to 9 mM (1.34 x 10(-8) A.mM(-1), r(2) = 0.99, RSD < 10%, n = 3), and the result w

290 521 within panel h were incorrectly given as mM and should have been given as microM.

291 nits of the x axis were incorrectly given as mM and should have been given as microM.

292 f acetyl-lysine mimetic ligands ranging from mM to low micromolar affinity that were identified using

293 ibited unprecedented sensitivity of 37.66 Hz/mM.cm(2) and a linear range of 1 to 20 mM.

294 the presence of thiols (e.g., glutathione in mM concentrations).

295 and the oxidant is very dilute (high nM-low mM).

296 h good selectivity, high-sensitivity (52 muA mM(-1)cm(-2)), low response time (<5s) and low detection

297 3) to 6.5 mM with a sensitivity of 191.6 muA mM(-1)cm(-2) and a detection limit of 1.1 x 10(-3) mM.

298 ion (mean +/- SEM) healthy: 3.9 +/- 0.02 muM/mM; completely tolerant: 3.83 +/- 0.04; partially tolera

299 mic-free [Mg(2+)] (free [Mg(2+)]cyto) passes mM levels.

300 resent at high concentrations (in the muM to mM range).