ライフサイエンスコーパス: fmol

1 luminometer format, mixtures containing 1.0 fmol total luciferase were quantified from measurements

2 is 0.5 fmol/100 mug DNA, and the LOQ is 1.0 fmol/100 mug DNA, making it possible to quantify bis-N7G

3 umor lysates with a linear range of 0.05-2.0 fmol/mug of total lysate protein and with coefficients o

4 burgdorferi lipoprotein at the level of 4.0 fmol of ospA/mg of serum protein.

5 o 15.5 +/- 5.0, 12 +/- 3.0, and 10.0 +/- 4.0 fmol/mg of tissue, respectively.

6 ease of NE in CMA at 16 Hz from 27.8 +/- 6.0 fmol/mg of tissue to 15.5 +/- 5.0, 12 +/- 3.0, and 10.0

7 urinary bladder (1.8 +/- 0.5 and 9.0 +/- 6.0 fmol/mg of tissue, respectively), and murine urinary bla

8 Detection limits (3SD) of 1.6, 3.2, and 7.0 fmol estimated from three procedure blanks were obtained

9 umarate (TDF), and they remained above 1,000 fmol/10(6) cells for as long as 7 days.

10 e maximum number of binding sites was 23,000 fmol/mg.

11 d agreement (0.48 +/- 0.01 and 0.29 +/- 0.02 fmol/mug of total protein) between immuno-MRM and immuno

12 detection limits as low as 0.1 fmol and 0.05 fmol for glycopeptides and phosphopeptides, respectively

13 earity of the fifth isotopologue (i.e., 0.05 fmol on column) was dependent on the peptide and instrum

14 sible signals for RNA amounts as low as 0.05 fmol.

15 run time (4 min), limit of detection (0.055 fmol on column, 18.75 fmol/ml plasma), precision (relati

16 tes of DNA methylation down to 0.34 +/- 0.06 fmol/s.

17 sensitivity (detection limits as low as 0.1 fmol and 0.05 fmol for glycopeptides and phosphopeptides

18 etection of melamine and Sudan I down to 0.1 fmol in water and toluene, respectively, using just 1 mu

19 in DNA samples with a detection limit of 0.1 fmol.

20 d be detected at a concentration down to 1.1 fmol L(-1).

21 n, achieving a detection limit of 55 pM (1.1 fmol), and the combined competitive-amplification latera

22 3.3 nM (+/-0.58), and receptor density, 10.1 fmol/mg (+/-0.64), was obtained with a saturation bindin

23 as low as 1.6 fmol for cow and goat, and 3.1 fmol for sheep PCR product were detected.

24 case, the sensitivity of the MS was about 1 fmol, which allowed us to achieve a spatial resolution o

25 ed with a detection limit of approximately 1 fmol/pixel from a variety of MALDI matrixes.

26 of the active form of MMP-12 to be around 1 fmol/mul in BALf from nanoparticle-treated mice.

27 assays with limits of detection as low as 1 fmol/L target DNA.

28 hat promotes cowpea ethylene production at 1 fmol leaf(-1) and triggers increases in the defense-rela

29 er assay (1 nM) and dynamic ranges between 1 fmol and at least 750 fmol (1-750 nM) were obtained.

30 Sample loadings ranging from 1 fmol to 10 pmol/spot were investigated.

31 and a quantification linearity range from 1 fmol to 20 pmol.

32 sulfate reduction rates are low enough (<<1 fmol H2Scell(-1)d(-1)).

33 4 fmol/muL), and sensitive (LLOD and LLOQ <1 fmol/muL).

34 Direct visualization of 1 fmol of target DNA molecules of interest was demonstrate

35 Limits of detection of 1 fmol per assay (1 nM) and dynamic ranges between 1 fmol

36 the optimized assay, a detection limit of 1 fmol was obtained.

37 tive form of MMP-12 down to a threshold of 1 fmol.

38 tings allows rapid enrichment from 5 mL of 1 fmol/muL phosphoprotein digests and concentration into s

39 When only 1 fmol of BSA was injected, one BSA peptide was consistent

40 ables complete Sanger sequencing from only 1 fmol of DNA template.

41 and showed high specific turnover rates (~1 fmol/(cell h)), high conversion yields (25%), and long-t

42 It also performed a higher sensitivity (1 fmol/muL IgG), a better enrichment capacity (up to ~300

43 was demonstrated at the level of less than 1 fmol of the peptide consumed.

44 hophora cells at rates between 0.02 and 0.10 fmol h(-1) cell(-1) and down to extracellular concentrat

45 specific lysine productivities were 2 and 10 fmol/cell/h.

46 This assay can reach a detection limit of 10 fmol and an isolation rate of 90% for the antigen CFP-10

47 rm also displayed a limit of detection of 10 fmol for thrombin in five different human serum samples

48 as achieved, with a limit of detection of 10 fmol/mL (0.64 ng/mL).

49 ents had AGT activity levels of less than 10 fmol/mg protein with a continuous-infusion O6-BG dose of

50 for concentrations of peptides lower than 10 fmol/microL, is to wash matrix/sample spots after peptid

51 fied in this work ranged from 110 pmol to 10 fmol per milligram of tissue protein.

52 The limit of detection for thrombin was 10 fmol in buffer using the aptamer/ISET-MALDI-MS configura

53 g detection limit for the full method was 10 fmol/mL (0.6 ng/mL).

54 The 1-10-fmol sensitivity and linear dynamic range allows quantit

55 Microinjection of BDNF (10-100 fmol) into the RVM facilitates nociception, which is dep

56 a high density of AT(1) binding (1207+/-100 fmol/g), which peaked at 0.4 mm rostral to the calamus s

57 allows a detection limit between 30 and 100 fmol DNA with a macroscopic gold disc electrode of 1 mm

58 y high loading capacities, approximately 100 fmol for angiotensin I and approximately 50 fmol for ins

59 nts resulted in sensitivities as high as 100 fmol of glycoprotein and 0.1 muL of human blood serum.

60 tics, and can detect biomolecules at sub-100 fmol mL(-1) concentrations.

61 the sample, was detectable at less than 100 fmol using EDTA-2D-RP/RP-nanoUPLC-MS/MS.

62 f spiked melamine in liquid milk down to 100 fmol also highlights the suitability of our SHP-OP SERS

63 of RNase B was fully characterized using 100 fmol of tryptic digest on a three-dimensional ion trap m

64 es and steroids down to the 800-amol and 100-fmol levels, respectively.

65 er incubation and that levels as low as 0.11 fmol of TPP per cell could be detected, suggesting the h

66 in those four ganglia are 481, 45, 9, and 11 fmol/mg protein, respectively.

67 5)I-labeled NmU (K(D) 364 pM and B(max) 1114 fmol/mg protein) was identified, and mRNA encoding NmU-1

68 - 18.0 nM and maximal binding of 348 +/- 112 fmol/mm(2)) to rat kidney AT1R.

69 increases in basal ECF ACh (from 105 to 118 fmol/min) and in the increase produced by atropine (from

70 ng agent, ionizing linearly from 150 to 1200 fmol (on-target) with a mean CV of 7%.

71 ion per zone loaded for fluorescence was 125 fmol for fluorescein isothiocyanate-labeled bovine serum

72 LOD for the above targets were 22.1 and 1260 fmol, respectively.

73 cal hyperinsulinemia (15 +/- 3 and 87 +/- 13 fmol x min(-1) x 100 ml(-1) basal vs. last 40 min of cla

74 ds to a detection limit of approximately 130 fmol of Intimin-ECD.

75 Adduct levels ranged from 0.43 to 131 fmol platinum/microg DNA in 140 samples; and adducts wer

76 f 3.7, 3.9, and 4.8% for 1.66, 6.65, and 133 fmol on column), and accuracy (97.5-104.5%).

77 ar over the range 0.23 to 19 nM (1.66 to 133 fmol on column).

78 compared with control subjects (166 vs. 133 fmol/ml, p=0.0003).

79 inear over a wide range (r > 0.99, 0.01-1384 fmol/muL), and sensitive (LLOD and LLOQ <1 fmol/muL).

80 mits of detection were determined to be 0.14 fmol for phenanthrene and 4 amol for caffeine and to a p

81 % (57.23 fmol/muL) of the total H3 HA (61.14 fmol/muL) in purified virus.

82 l/punch (IQR:691, 1166) in pregnancy vs 1406 fmol/punch (IQR:1053, 1859) postpartum (p=0.006).

83 ted macaques receiving TAF PrEP (351 and 143 fmols/106 cells, respectively; P = .921).

84 l/punch (IQR: 667,1105) in pregnancy vs 1438 fmol/punch (IQR: 1178,1919) postpartum.

85 lumn limits of detection between 0.55 and 15 fmol.

86 A brushes allow detection of as little as 15 fmol of phosphopeptide.

87 to over 3 mM (0.15 pmol) and 500 microM (15 fmol) for fluorescein and TRITC-tagged albumin solutions

88 (358 fmol) and protein (ranging from 7 to 15 fmol depending on the assayed protein).

89 to 44.8 nmol x person(-1) x min(-1) (16-1530 fmol x cm(-2) x min(-1)).

90 .1 (95% CI, 1.3-3.3; P = .002) versus >=1650 fmol/punch, respectively.

91 rticipants with TFV-DP <800 and 800 to <1650 fmol/punch were 4.7 (95% CI, 2.6-8.7; P < .0001) and 2.1

92 t of 2 nM and maximum binding capacity of 18 fmol/10(6) cells, and (18)F-FES had a dissociation const

93 ol vs. +AnxA4: 1956 +/- 162 vs. 1304 +/- 185 fmol/microg protein; n = 8).

94 P < .0001) for a TFV-DP concentration >=1850 fmol/punch compared to <350 fmol/punch.

95 tomole range with a limit of detection of 19 fmol.

96 alysates rose from 73 fmol/min to 148 or 197 fmol/min (P<0.05).

97 itive with a limit of detection (LOD) of 0.2 fmol and a quantification linearity range from 1 fmol to

98 absolute quantification of as little as 0.2 fmol of miR-203.

99 loped a simple, sensitive (approximately 0.2 fmol on column) and specific GC-MS assay for the detecti

100 ct DNA detection, with the new LoD being 1.2 fmol (or 26 fg/muL or 2 pM).

101 crol of liquid is required, as little as 1.2 fmol of trypsin can be detected by using the on-chip ass

102 7.1 +/- 0.7, 26.5 +/- 4.5, and 15.1 +/- 3.2 fmol/mg of tissue, respectively.

103 A detection limit (3 SD) of 7.2 fmol estimated for ID LC-ICPMS with a 10 muL injection v

104 wells, the limit of detection (LOD) was 7.2 fmol of DNA target, corresponding to a final concentrati

105 peptidases (degradation rate of 100 +/- 8.2 fmol min(-1) mg(-1)) but an excellent substrate for phos

106 ction for phosphopeptides is approximately 2 fmol, based on using matrix-assisted laser desorption/io

107 of single cell with sensitivity as low as 2 fmol.

108 and 14 peptide identifications (IDs) when 20 fmol was loaded.

109 were calculated to be approximately 0.4 (200 fmol) and 0.8 microM (400 fmol), respectively.

110 ntified for standard I by consuming only 200 fmol of each protein.

111 ulted in an increased dynamic range (15-2000 fmol on plate) and improved linearity (r(2) = 0.99).

112 ressed at similar levels (approximately 2000 fmol/mg) and bound the radioligand [(3)H]R(+)-7-chloro-8

113 32 smoker samples (mean +/- SD, 179 +/- 205 fmol/micromol dAdo).

114 issue)(-1)) relative to controls (234 +/- 21 fmol (mg tissue)(-1)), and sepiapterin elevated flow-med

115 erved for Arg-389 (435 +/- 80 vs. 115 +/- 23 fmol per well).

116 n control animals, NET B(max) was 388 +/- 23 fmol/mg protein and HED heart uptake (HU) at 30 min was

117 uL) from the commercial TIV and 93.6% (57.23 fmol/muL) of the total H3 HA (61.14 fmol/muL) in purifie

118 inimally EC90 protective concentration of 24 fmol/10(6) cells.

119 detection limit was of 12.0 nmol L(-1) (240 fmol in the sample).

120 hput assay for ACK1 capable of detecting 240 fmol per well of the kinase reaction product employing a

121 A low detection limit of 240 fmol in 2 mL of SSC buffer was achieved.

122 nM) and receptor concentration (296 vs. 243 fmol/mg).

123 ic small RNA was detected in amounts of 0.25 fmol (i.e. concentration of 10 pM in a 25 microl reactio

124 (1:3500) and limit of detection down to 0.25 fmol.

125 o 66 kDa) with a detection limit of 8 and 25 fmol for verapamil and reserpine, respectively, and quan

126 We were able to detect 25 fmol of Rhodamine in agar ablation experiments.

127 imit (signal/noise ratio of 3) of 0.5 nM (25 fmol on column).

128 on of 5 nM solution containing a total of 25 fmol labeled analyte.

129 to 250 pmol, with a limit of detection of 25 fmol on column for all analytes except 2-AG, noladin eth

130 Linearity was proven over the range of 25 fmol to 250 pmol, with a limit of detection of 25 fmol o

131 osylation structures, was obtained at the 25 fmol level.

132 trols (mean [SD], 0.70 [0.33] vs 1.93 [1.25] fmol/mg, respectively; P = .001).

133 accumulation at a rate of approximately 250 fmol/min/cm2, reflecting the basal ATP release rate.

134 he method is able to detect as little as 250 fmol of target without using PCR and exhibits single nuc

135 es except 2-AG, noladin ether, and 2-LG (250 fmol).

136 ep with purified H3 HA captured 82.9% (55.26 fmol/muL) of the total H3 HA (66.69 fmol/muL) from the c

137 t of detection (LOD) of 4.7 ppm (for only 26 fmol H2).

138 (with a K(D) of 2.97 nM and a B(max) of 2619 fmol/mg protein).

139 tection limit of 0.14 nM corresponding to 28 fmol of analyte.

140 ted BK 1-5 (160 +/- 75 fmol/mL, vs 44 +/- 29 fmol/mL in controls) and angiotensin II (182 +/- 41 pg/m

141 e units or 500 nM bromophenol blue (BPB) (29 fmol) was achieved using only an optical microscope and

142 and binding data reports low NOP density (29 fmol mg(-1) protein) in dog.

143 ass IV patients as determined by POCTs (>290 fmol/ml) nano-LC-electrospray ionization-FT-ICR-MS data

144 I increased cGMP accumulation by 4.9 +/- 1.3 fmol/microg (p < 0.01).

145 re the rate of in vitro RNA synthesis (~10.3 fmol of RNA per minute).

146 se-derived sphingosine-NDA were 9.6 and 12.3 fmol, respectively, and the limits of quantification wer

147 d peptide with a method detection limit of 3 fmol.

148 e as evidenced by the detection of 100 pg (3 fmol) of a test protein spiked into 1 microg of a comple

149 approximately 300 pM of DNA target, i.e. 30 fmol in a 100 muL sample) and excellent selectivity, all

150 scope detection platform offered a LOD of 30 fmol and a dynamic range spanning 3 orders of magnitude.

151 ) hepatocytes, but reaches a limit at 90-300 fmol.

152 f detection of the assay was found to be 300 fmol with the upper limit of the dynamic range at 5 pmol

153 IL and was nontoxic at doses ranging from 32 fmol/kg to 3.2 pmol/kg.

154 n full scan mode, detection limits of 0.1-33 fmol were achieved for glycoloytic and tricarboxylic aci

155 ent Michaelis-Menten parameters of Vm = 0.34 fmol/s and kcat/Km on the order of 104 s-1 M-1, in agree

156 the limit of detection of the method was 34 fmol, which is a significant improvement in comparison t

157 . anxA4a(-/-): 1891 +/- 238 vs. 2796 +/- 343 fmol/microg protein; n = 9-10).

158 aried from below the limit of detection (350 fmol/g) to 15 pmol/g wet brain.

159 entration >=1850 fmol/punch compared to <350 fmol/punch.

160 direct measurement of sulfur with ICPMS (358 fmol) and protein (ranging from 7 to 15 fmol depending o

161 The results provide a detection limit of 36 fmol for step-scan SIR measurements of ferrocyanide.

162 covery of 90% and a limit of detection of 38 fmol per single spot sampled.

163 increased ACh concentrations from 81 to 386 fmol/min in control rats and from 137 to 680 fmol/min in

164 ly reduced renal VDR levels, from 555 to 394 fmol/mg protein (29%, P < 0.001).

165 with K(d) of 3.64 nmol/L and B(max) of 120.4 fmol per million cells.

166 asma brain natriuretic peptide levels (-19.4 fmol x ml(-1); 95% CI, -5, -34; p = 0.014) and improveme

167 urinary bladder (1.4 +/- 0.1 and 6.2 +/- 2.4 fmol/mg of tissue, respectively).

168 1.6 +/- 27.4 versus LP n = 7, 445.7 +/- 27.4 fmol (mg glomerular protein)(-1), P < 0.01), but affinit

169 fication of FodU at a detection limit of 3-4 fmol, which is approximately 20-fold better than that fo

170 were between 0.04 to 0.5 nmol/L (0.2 to 3.4 fmol) at a signal-to-noise ratio of 3.

171 lso improved dramatically using SPE (8 and 4 fmol/ml) compared with organic extraction (25 and 18.75

172 e than those grown aerobically (1.3 x 10(-4) fmol/cell vs 7.9 x 10(-6) fmol/cell; P < 0.01).

173 ssay was validated in a linear range from 40 fmol to 200 pmol 5mdC.

174 The molecular weight determination of 40 fmol/microL apomyoglobin was determined in 3 s using a r

175 oximately 0.4 (200 fmol) and 0.8 microM (400 fmol), respectively.

176 cids were measured and ranged from 30 to 400 fmol islet(-1) min(-1).

177 ol subjects (181 +/- 7 fmol/g vs. 262 +/- 41 fmol/g; p < 0.05).

178 ith a maximum binding capacity (Bmax) of 414 fmol/10(6) cells (2.5 x 10(5) GRP-R/cell).

179 EAS-2B cells occurred at a median rate of 43 fmol min(-1) mg(-1) resulting in a mean half-life of 20

180 CV) of 5%, and a quantification limit of 432 fmol.

181 8 h reduced renal VDR levels from 515 to 435 fmol/mg protein (15%, P < 0.03) in wild-type mice.

182 OD of the assay in a sandwich format was 450 fmol with a dynamic range spanning 2 orders of magnitude

183 microM) for penicillin and ampicillin to 455 fmol (350 microM) for histidine were obtained.

184 1 min with detection limits of 0.54 and 1.47 fmol for 5mdC and 2dG, respectively.

185 ion limit was determined to be as low as 0.5 fmol in 80 microg DNA, corresponding to 9 adducts/10(9)

186 copic responses being derived from just ~0.5 fmol of material.

187 pable of reliably detecting as little as 0.5 fmol of protein, and protein differences down to +/- 15%

188 gnitude across the gradient (500 fmol to 0.5 fmol on column) and no systematic trend was observed for

189 Detection limits as low as 0.5 fmol were obtained, with lower possible if a smaller sam

190 The LOD value of the new method is 0.5 fmol/100 mug DNA, and the LOQ is 1.0 fmol/100 mug DNA, m

191 race peptides at levels of approximately 0.5 fmol/microL in complex peptide mixtures with a wide dyna

192 +/-0.3 to 3.1+/-1.0, 5.9+/-1.2 and 5.3+/-0.5 fmol/mL (P=nonsignificant, P<0.0001, and P<0.0001, respe

193 tained in 10 mug of DNA hydrolysates was 1.5 fmol, which corresponded to 50 adducts/10(9) normal nucl

194 e allowed for the sensitive detection of 2.5 fmol of methylated target dsDNA in 5 min.

195 easurement of high quality IR spectra of 2.5 fmol of molecules confined to a 125 mum(2) beam spot.

196 ximately 50 pM in 50 muL ( approximately 2.5 fmol).

197 for SMN1 and uidA target were 54.3 and 30.5 fmol, and when the probe ratio was 4:1, the LOD for the

198 grees C of calculated temperature over a 5.5 fmol.cell(-1).d(-1) increase in varphi.

199 in was detected with an LOD of 300 nM or 7.5 fmol injected.

200 imits of detection of 3.6, 1.6, 5.8, and 8.5 fmol for estradiol, androstendione, testoterone, and pro

201 observed with TM-AFM and CV coincide (2-8.5 fmol.cm(-)(2)), indicating that most-if not all-cbo(3) o

202 he PB/AChE-ChO electrode was 5 microM or 9.5 fmol.

203 cation of DHEA, E2, and T with 10, 10, and 5 fmol lower limits of quantification and linear ranges to

204 test compound, 1.6 pmol of substrate, and 5 fmol of enzyme per reaction.

205 tely 10% (relative standard deviation) and 5 fmol on-column, respectively.

206 on spectra were obtained with as little as 5 fmol of peptides.

207 As few as 5 fmol of VEGF(165) could be detected by the naked eye wit

208 The detection limit is 5 fmol for the synthetic single-stranded DNA.

209 analytes and with high sensitivity (LOD of 5 fmol for caffeine).

210 -8) M, consumes very little sample (< or = 5 fmol), and offers capillary interfaces with various sepa

211 d the limits of detection to be in the 2.5-5-fmol range.

212 cases (mean [SD], 16.2 [2.0] vs 29.6 [16.5] fmol/mg, respectively; P = .04) or with male and female

213 fmol for angiotensin I and approximately 50 fmol for insulin, were obtained with a 4.2 m x 10-microm

214 ected with a lower limit of approximately 50 fmol of complement and was sufficiently selective to dif

215 nrichment with sensitivity assessed to be 50 fmol.

216 A detection limit of 50 fmol M(1)GdR/ml urine is achieved starting with 5 ml of

217 ntitative assay with a detection limit of 50 fmol of target DNA.

218 However, it was found that with less than 50 fmol of biotin-labeled nucleic acid, which corresponds t

219 apable of reliable detection of less than 50 fmol of the derivatives of S1P and DHS1P without signifi

220 ut a measurement is very small, less than 50 fmol, which would be a useful attribute for drug screeni

221 ial samples were easily detected, down to 50 fmol on column.

222 of detection of the setup (approximately 500 fmol limit of detection for citric acid), improvements i

223 with concentrations at 3 days exceeding 500 fmol/10(6) mononuclear cells.

224 orders of magnitude across the gradient (500 fmol to 0.5 fmol on column) and no systematic trend was

225 for the total ion current peak areas of 500 fmol of angiotensin I were improved by a factor of 2.6 w

226 ng platform allowed for detection down to 53 fmol of Streptococcus pneumoniae tmRNA, equivalent to ap

227 ch prostaglandin was 20 pg/ml (0.20 pg, 0.55 fmol on-column), and the interday and intraday coefficie

228 a limit of quantification at lower than 0.56 fmol/muL.

229 crease produced by atropine (from 489 to 560 fmol/min; P<0.05).

230 (9.3 +/- 0.6, 10.1 +/- 0.5 and 10.3 +/- 0.6 fmol mg(-1) protein, respectively), but there were no so

231 vs. anxA4a(-/-): 5.1 +/- 0.3 vs. 6.7 +/- 0.6 fmol/microg protein) or FSK (anxA4a(+/+) vs. anxA4a(-/-)

232 ely cow, sheep and goat, while as low as 1.6 fmol for cow and goat, and 3.1 fmol for sheep PCR produc

233 in the samples collected before EFS (0.2-1.6 fmol/mg of tissue).

234 on-column, equivalent to 8 pg/mL (26.5-29.6 fmol/mL) in the original serum sample.

235 detection limits ever published (11 and 6.6 fmol, respectively).

236 Detection limits ranging from 6 fmol (5 microM) for penicillin and ampicillin to 455 fmo

237 ally (1.3 x 10(-4) fmol/cell vs 7.9 x 10(-6) fmol/cell; P < 0.01).

238 model system, and a limit of detection of 62 fmol is achieved.

239 one AF and control subjects (1,730 vs. 1,625 fmol/ml, p=0.90).

240 ties of AT(1) binding, 278+/-38 and 379+/-64 fmol/g, respectively.

241 tion limits of detection were as low as 1.65 fmol.

242 found that human lung macrophages contain 66 fmol of this protein per 100 microg of cell protein.

243 fmol/min in control rats and from 137 to 680 fmol/min in those consuming UMP (P<0.05).

244 % (55.26 fmol/muL) of the total H3 HA (66.69 fmol/muL) from the commercial TIV and 93.6% (57.23 fmol/

245 but increased in control subjects (181 +/- 7 fmol/g vs. 262 +/- 41 fmol/g; p < 0.05).

246 limits of quantification were 34.2 and 45.7 fmol, respectively.

247 As little as 70 fmol glycan species can be detected and identified.

248 h a high degree of anti-HIV protection (>700 fmol/punch) were found in 42 (54%), 37 (47%), 38 (49%),

249 ir diphosphate (TFV-DP) concentrations >=700 fmol/punch (consistent with >=4 doses/week) assessed at

250 h levels in striatal dialysates rose from 73 fmol/min to 148 or 197 fmol/min (P<0.05).

251 R(-/-) mice have elevated BK 1-5 (160 +/- 75 fmol/mL, vs 44 +/- 29 fmol/mL in controls) and angiotens

252 it of detection (0.055 fmol on column, 18.75 fmol/ml plasma), precision (relative standard deviations

253 mpared with organic extraction (25 and 18.75 fmol/ml plasma).

254 namic ranges between 1 fmol and at least 750 fmol (1-750 nM) were obtained.

255 57 versus 1001 +/- 31 or versus 1315 +/- 76 fmol/nmol/h, P <.0001).

256 ith a detection limit of 1.3 ng/ml (i.e. 0.8 fmol in used sample volume of 10 microl).

257 12.9 +/- 0.9, 13.5 +/- 0.9 and 13.6 +/- 0.8 fmol mg(-1) protein, respectively) and Arg16+Gln27 havin

258 ring EFS of CMA (2.5 +/- 0.9 and 5.8 +/- 0.8 fmol/mg of tissue, respectively), canine urinary bladder

259 highest in the amygdala (B(max)=149.9+/-13.8 fmol/mg protein), thalamic, and hypothalamic nuclei.

260 nly 7 of 30 nonsmoker samples (15.5 +/- 33.8 fmol/micromol dAdo; P < 0.001).

261 numbers in both the stimulated (35.2 +/- 4.8 fmol acetylcholine receptor/mg protein) and nonstimulate

262 lower in arterioles from old rats (94 +/- 8 fmol (mg tissue)(-1)) relative to controls (234 +/- 21 f

263 ers of magnitude with a detection limit of 8 fmol of toxin is achieved.

264 le controls combined (mean [SD], 53.9 [19.8] fmol/mg; P = .005).

265 tection of LD/LI/ToF-MS as low as [0.2, 2.8] fmol per laser pulse and we make quantitative prediction

266 ) = 7.62 +/- 1.18 nM, B(max) = 31.6 +/- 1.80 fmol/mg protein) that is distinct from fatty acid amide

267 tly showed high TFV-DP levels (median, 1,810 fmol/10(6) cells) between 4 and 24 h that exceed the 95%

268 5 nM) specifically bound to B-CK (2330+/-815 fmol mg protein(-1)).

269 tant of 3 nM and maximum binding capacity 83 fmol/10(6) SKOV3 cells.

270 ates can be measured as low as 3.55 +/- 1.84 fmols(-1) in a 96-well plate format, and the assay has b

271 e concentration(50) values of 68, 45, and 87 fmol leaf(-1) for Vu-In, Vu-(E+)In, and Vu-(GE+)In, resp

272 Modelled median steady-state TFV-DP was 881 fmol/punch (IQR: 667,1105) in pregnancy vs 1438 fmol/pun

273 2.2 lesions per 10(8) nucleotides (nts, 0.9 fmol on column).

274 initial reaction rates averaged 3.9 +/- 2.9 fmol AngII/min/ micro g protein with a mean maximal conv

275 4.7, and 1.93 ng/mg HSA (1010, 220, and 28.9 fmol BPDE equiv/mg HSA)--were significantly different (P

276 endothelin-1 (80 +/- 15.7 versus 29 +/- 3.9 fmol/kg body wt per d; P < 0.02) and of the NO metabolit

277 the series (intrathecal ED50 approximately 9 fmol per mouse), whereas in untreated mice its ED50 was

278 obtained in the concentration range of 10-90 fmol/microL.

279 r format provided a limit of detection of 90 fmol and an upper limit of dynamic range of 3.5 pmol.

280 ut still significant increase (from 75 to 92 fmol/min, P<0.05), and elevated striatal ACh content (by

281 Observed median steady-state TFV-DP was 965 fmol/punch (IQR:691, 1166) in pregnancy vs 1406 fmol/pun

282 of GSH in HepG2 cells to be 14.96 muM (2.99 fmol/cell).

283 l-D-glucose uptake into erythrocytes was 996 fmol/10(6) red blood cells per second, significantly les

284 ective detection of the peptide biosensor at fmol levels from aliquots of cell lysate equivalent to ~

285 oteinase inhibitor proteins when supplied at fmol levels to young tomato plants through their cut ste

286 With a detection limit of a few fmol mm(-2), and the possibility for sub-fmol detection

287 species involved in the redox process (e.g., fmol/cm(2), 0.1% of a full protein monolayer).

288 f unique, long oligonucleotides (150mers) in fmol amounts using parallel synthesis of DNA on microarr

289 20 matched controls with no IFTA (mean log2[fmol/umol of creatinine], bone marrow stromal cell antig

290 es can be simultaneously quantified from low fmol/muL to nmol/muL levels in cellular samples.

291 marked increase in analytic sensitivity (low fmol/muL) and the identification of double bond position

292 markedly increases analytic sensitivity (low fmol/muL).

293 aterial and has a detection limit in the low fmol range, and is thus the most sensitive method for di

294 ompounds with limit of detection down to low fmol levels, capability of analyzing small and large mol

295 ibody bead, (ii). detecting peptides at low (fmol) levels, (iii). producing MS/MS data of suitable qu

296 y (maximum number of binding sites [B(max)], fmol/mg protein) for each heart.

297 d and chemotherapy-resistant BPL at nontoxic fmol/kg dose levels.

298 urces and lowest sample amount requirements (fmol range).

299 few fmol mm(-2), and the possibility for sub-fmol detection sensitivity, this measurement technique e

300 trochemical stripping transduction (to yield fmol detection limits) and with an efficient magnetic se