ライフサイエンスコーパス: microliter

1 njections of either glutamate or saline (0.5 microliter).

2 ble for small volume samples (few to hundred microliter).

3 DA assay (1 contaminating molecule per assay microliter).

4 low and sensitivity high (279 pg iron in 100 microliters).

5 dividing by volume of posterior aqueous (60 microliters).

6 blood eosinophil count of less than 1000 per microliter.

7 spinal fluid contained at least 500 RBCs per microliter.

8 n absolute neutrophil count of 100 cells per microliter.

9 eripheral blood CD4(+) cell counts above 200/microliter.

10 nd decline of CD4(+) T cells to </=200 cells/microliter.

11 en blood CD4(+) T-cell counts fell below 300/microliter.

12 vant limit of detection of 500 parasites per microliter.

13 00 CD3(+) autologous circulating T cells per microliter.

14 mall area from applied volumes as low as one microliter.

15 uid containing 2.08 x 10(6) viral copies per microliter.

16 kBq range in a constant sample volume of 580 microliters.

17 ato leaves with the sample volume of several microliters.

18 nano-molar/L range and the volume of tens of microliters.

19 pioid antagonist naloxone (0.1-1.0 microgram microliter-1 at 2 microliters min-1) onto the exposed ve

20 ventricular infusion of butorphanol (26 nmol microliter-1 h-1) via osmotic minipumps for 3 days.

21 ceptor agonist, SKF 82958 (2.0 microgram 0.5 microliter-1 side-1) on the acquisition and expression o

22 tor antagonist, SCH 23390 (2.0 microgram 0.5 microliter-1 side-1), on the acquisition and expression

23 trodialysis of naloxone (0.1-10.0 micrograms microliter-1) onto the supraoptic nucleus of rats made d

24 vial fluid averages 3.62 +/- 0.19 micrograms microliters-1, the endogenous synovial fluid volume was

25 39th that for Ringer solution (1.94 +/- 0.01 microliter 2O-1 ).

26 er, administration of LY288513 (17 nmol/0.25 microliter) 55 min prior to pentagastrin (1.0 nmol/0.25

27 en-20-yn-3-one; 3.0, 10.0, or 30.0 ng in 0.5 microliter) administered into the dorsal hippocampus of

28 th the incidence of parasitemia > or = 5,000/microliter (age-adjusted r2 = 0.72, p < 0.001).

29 CA3 area of the dorsal hippocampus) with 5.0 microliters aggregated A beta in suspension, and the rem

30 Ten 100-microliters aliquots of this solution were counted in a

31 ophosphate (8-bromo-cAMP) (0.2-7 nmol in 0.2 microliter) alone or together with the alpha1-adrenocept

32 imes higher rate of parasitemia > or = 5,000/microliter among children exposed to > or = 1 infective

33 We developed a simple pairing scheme using microliter amounts of E. coli osmotic shockates bearing

34 , it is possible to measure BCAT activity in microliter amounts of rat tissue homogenates.

35 system is generally useful for separation of microliter amounts of unreactive trace volatile compound

36 tients with CD4+ T-cell counts of 200 to 900/microliter and 2- to 10-year histories of HIV-1 infectio

37 ained at least 10 red blood cells (RBCs) per microliter and bloody LP as one in which the cerebrospin

38 rum containing 6.10 x 10(2) viral copies per microliter and influenza A virus in lung lavage fluid co

39 ow that in contrast to techniques delivering microliter and nanoliter volumes, evaporation has a majo

40 gle-cell RNA amplification methods with both microliter and nanoliter volumes, using sequence from bu

41 rum containing 2.50 x 10(8) viral copies per microliter and porcine respiratory coronavirus (PRCV) in

42 ystem that performs rapid thermal cycling of microliter and smaller liquid volumes inside glass capil

43 ents with CD4(+) T cell counts >/= 350 cells/microliter and viral load below the limits of detection

44 covery of analyte can be achieved with a few microliters and conducted until steady-state is attained

45 umbers in children with malnutrition (28 per microliter) and a recovery in cell number (48 per microl

46 ols developed low CD4(+) T-cell counts (<200/microliter) and AIDS.

47 nia virus particles (down to 60 virions in a microliter) and distinguish them from nonviable viruses

48 que requires a minimal protein amount (a few microliters) and allows monitoring the bound Cu(II) ions

49 Aliquots of normal saline (1 x NS, 100 microliters) and higher concentrations (3 x NS, 6 x NS,

50 termined adult rat vitreous volume (56 +/- 2 microliters) and that of previous reports.

51 amine (0.0, 2.0, 10.0, or 20.0 microgram/0.5 microliter), and lever pressing was tested in the absenc

52 w cost, flexibility, low volume samples (few microliters), and homogeneous format.

53 arasitemia, time to parasitemia > or = 5,000/microliter, and parasitemia density.

54 Fifteen minutes before each x-ray, 150 microliters aqueous humor was removed from the anterior

55 icroinjection of IL-1ra (50 microgram in 0.5 microliter at 0 + 1 h) into the anterior hypothalamus (A

56 3, 7 and 10 days after the injection of 100 microliter autologous blood in the right basal ganglia.

57 In the second study, 100 ng/microliter bicuculline administered unilaterally prior t

58 However, 250 ng/microliter bicuculline produced motor dyskinesias and/or

59 ared (NIR) fluorescence detection to analyze microliter biological samples with an amol limit of dete

60 hours after injection of IL-1beta (1 ng in 1 microliter), cerebral blood volume was significantly inc

61 om milliliter aqueous samples and performing microliter chemical amplification, serial enzymatic reac

62 s can serve as well-mixed, easily controlled microliter chemical reactors for characterizing homogene

63 m the anterior chamber and replaced with 150 microliters citrate buffer containing 0 mM or 100 mM TEM

64 TOP (mu-selective antagonist, 5 micrograms/2 microliters) completely blocked the effects of morphine

65 ssful in testing dose-response analysis, the microliter consumption of expensive reagents and hours o

66 tz capillary mixer with an approximately 0.5 microliter delivery volume to the midpoint of the EPR-ac

67 55 min prior to pentagastrin (1.0 nmol/0.25 microliter) delivery blocked the facilitatory effects of

68 A hanging microliter drop of 1-octanol is shown to be an excellent

69 an infrared (IR) laser from the surface of a microliter droplet deposited on a stainless steel post.

70 temporal polymerase chain reaction (PCR) in microliter droplets.

71 e Langmuir model and tensiometry results for microliter drops.

72 mple system (RSS), a convection platform for microliter drops.

73 and concentration into small-volume (tens of microliters) eluates.

74 y active in minuscule water droplets (1 to 3 microliters) entrapped in oil.

75 gonist, pentagastrin, (0.5 and 1.0 nmol/0.25 microliter) facilitated the occurrence of defensive rage

76 -B antagonist, LY288513 (4.2, 17.0 nmol/0.25 microliter), facilitated the occurrence of predatory att

77 appa-selective antagonist, 73.5 micrograms/2 microliters) failed to block the effects of morphine.

78 blood eosinophil count of less than 600 per microliter for 8 or more consecutive weeks was achieved

79 rain transfer constant of AraC was 2.5+/-1.4 microliter g(-1) min(-1), compatible with high water sol

80 hetized rabbits at various time points via a microliter glass capillary tube, and the miniature senso

81 the levels of [3H]IP at 0.3 to 3 micromol/8 microliter i.c.v. with lower doses resulting in less eff

82 nt, pertussis toxin treatment (1 microgram/5 microliter, i.c.v.; 48 hr before the 8-OH-DPAT challenge

83 roliter, icv, n=8), prazosin (10 microgram/5 microliter, icv, n=12) or alpha-helical CRF(9-41) (10 mi

84 Yohimbine (3 microgram/5 microliter, icv, n=8) pretreatment did not alter hemodyn

85 etreatment with phentolamine (30 microgram/5 microliter, icv, n=8), prazosin (10 microgram/5 microlit

86 ) or alpha-helical CRF(9-41) (10 microgram/5 microliter, icv, n=9) prevented the decrease in cardiac

87 itemia level of fewer than ten parasites per microliter in a volume below 10 mul of whole blood is de

88 ive intermediate monocytes to >100 cells per microliter in patients with sarcoidosis and a fivefold d

89 analytes from small sample volumes of a few microliters in an automated and high-throughput manner,

90 s only 2% of all Tregs (one to six Tregs per microliter) in peripheral blood but, when isolated, exhi

91 nnabinoid agonist CP55,940 (5 microgram/0.25 microliter) induced strong contralateral turning when mi

92 Two-microliter injections of succinylcholine chloride in a 5

93 ceived N-methyl-D-aspartate (NMDA, 0.5 M/0.5 microliter) injections in the areas of RRN and vMPJ to p

94 microliter) or intracaudate (2 microgram/0.5 microliter) injections of either glutamate or saline (0.

95 ic antagonist atropine (0.5 microgram in 0.2 microliter) into either the ipsilateral or contralateral

96 following injection of MK-801 (2 microgram/3 microliter) into the fourth ventricle.

97 or antagonist atenolol (0.5 microgram in 0.2 microliter) into the ipsilateral, but not the contralate

98 d subcutaneous injections of 5% formalin (50 microliter) into the plantar surface of the right hind p

99 using microinjections of Fluoro-Gold (8%, 6 microliters) into the PAG were employed to identify the

100 the CCK-A antagonist, PD140548 (34 nmol/0.25 microliter), into the PAG failed to alter response laten

101 agonist, LY288513 (1.05, 4.2, 17.0 nmol/0.25 microliter), into the PAG suppressed the hissing respons

102 Delta(9)-THC (15-30 microgram/microliter intracerebellar) resulted in a significant mo

103 bolished Delta(9)-THC (15 and 25 microgram/1 microliter intracerebellar)-induced motor impairment.

104 l min-1 cmH2O-1; post-enzyme, 3.11 +/- 0.45 microliter l min-1 cmH2O-1).

105 lining by 2.3 times (control, 1.34 +/- 0.22 microliter l min-1 cmH2O-1; post-enzyme, 3.11 +/- 0.45 m

106 vicurvature, and extremely low (0.0005-0.001 microliter L-1) ethylene concentrations can restore the

107 tive stress induced by clinical drugs at the microliter level.

108 tection limits down to the low femtomole per microliter levels were achieved for propafenone and vera

109 ynovial fluid volume was calculated to be 50 microliters (mass/concentration), about double the aspir

110 olated from whole blood in silicon-glass 4.5-microliter microchips containing a series of 3.5-micron

111 resonator were utilized to measure PP(*) in microliter microdialysis samples (LOD 0.36 pmol).

112 he slope of the quasi-plateau, 0.05 +/- 0.01 microliter min-1 cmH2O-1 (mean +/- s.e.m.), was 1/39th t

113 At a flow rate of 5 microliter min-1, arteries from the WKY dilated signific

114 aloxone (0.1-1.0 microgram microliter-1 at 2 microliters min-1) onto the exposed ventral surface of t

115 ly with time, to the lowest value of 44+/-11 microliter/min at the end of the experiment.

116 /-S.D.) value for CSF production was 51+/-10 microliter/min initially and decreased significantly but

117 rank tap water, left kidney GFR averaged (in microliter/min per 100 g body wt) 503 +/- 78 (n = 9) in

118 microdialysis probes (3 mm; flow rate of 2.1 microliter/min) implanted in the left hippocampus.

119 /-6, 42+/-8, 38+/-6, 37+/-6, 36+/-5, 36+/-5, microliter/min, respectively, from 15 to 165 min.

120 basolateral) reduced JWL-->B from 6.1 to 4.4 microliter/min/cm2 (p < 0.05, n = 5) and abolished the P

121 roM luminal) reduced JWL-->B from 5.7 to 3.7 microliter/min/cm2 (p < 0.05, n = 5) and reduced PD by 4

122 The JWL-->B (6.1 microliter/min/cm2) was larger than JWB-->L (4.5 microli

123 oliter/min/cm2) was larger than JWB-->L (4.5 microliter/min/cm2, p < 0.05, n = 30).

124 liters/minute +/-0.2; after pilocarpine, 3.6 microliters/minute +/- 0.2.

125 Control flow was 3.9 microliters/minute +/- 0.4; after timolol, 2.5 microlite

126 croliters/minute +/- 0.4; after timolol, 2.5 microliters/minute +/-0.1; after methazolamide, 2.4 micr

127 ters/minute +/-0.1; after methazolamide, 2.4 microliters/minute +/-0.2; after pilocarpine, 3.6 microl

128 is (7,718 and 21,612 copies of viral RNA per microliter nasal wash, respectively; P = 0.48).

129 study, unilateral administration of 10-50 ng/microliter of bicuculline did not alter behavior.

130 In the third study, 75 ng/microliter of bicuculline was administered unilaterally

131 h) monocytes rose from 64+/-5 to 108+/-9 per microliter of blood (P<0.05).

132 formed, as few as six bacteria spiked in 200 microliter of blood could be detected.

133 cells, with an average of 100 cells lost per microliter of blood per year.

134 rasitemia (peak parasitemia, </=20 parasites/microliter of blood).

135 the number of responding CD8(+) T cells per microliter of blood.

136 had CD4+ lymphocyte counts of > or = 500 per microliter of blood.

137 od cell count can be defined directly from a microliter of crude whole blood.

138 Oligosaccharide samples equivalent to 1 microliter of human milk give optimum chromatographic se

139 tection down to 50 femtogram of PFCs, in one microliter of human plasma.

140 diolabeled ATP and ATPase activity in 3.5 ng/microliter of membrane protein.

141 quantifiable by Western blot in less than a microliter of plasma from lung cancer patients.

142 ) probing 12 independent areas with a single microliter of processing liquid and (ii) processing a 2

143 27 gauge cannula, which was used to infuse 1 microliter of saline over 5 min.

144 coli 16S rRNA gene was achieved by adding 5 microliter of undiluted processed sample DNA to a 50-mic

145 of parasitemia (no. of asexual parasites per microliter of whole blood), sensitivities were 83% (>0 t

146 n the multi-analyte formate are 44 fmol (100 microliters of 0.1 ng/ml TNT solution) and 224 fmol (100

147 entrally through the tear film and cornea, 2 microliters of 0.35% F were instilled and 10 fluorescenc

148 of 0.1 ng/ml TNT solution) and 224 fmol (100 microliters of 0.5 ng/ml RDX solution), respectively.

149 rapid digestion of particulate metals using microliters of acid added directly to a punch taken from

150 kappa light chains that requires only a few microliters of biological material.

151 ic acid in human blood, where only dozens of microliters of blood (few drops) was required, demonstra

152 ot of conditioned medium in culture or a few microliters of blood in vivo at different time points.

153 globin and its tryptic digests directly from microliters of blood, achieving a detection limit of les

154 ated by detecting allergen-specific IgE from microliters of characterized human serum and unprocessed

155 One hundred microliters of dual-labeled liposomes (DLLs) containing

156 ion of T-lymphocyte proliferation, 20 nmol/2 microliters of either morphine sulfate or DAMGO (mu-sele

157 Approximately 100 mg of solid stool or 200 microliters of liquid fecal sample was thoroughly suspen

158 o a paper strip to evaporate off hundreds of microliters of liquid to concentrate the target analyte.

159 d to enable analysis of nucleobases in a few microliters of liquid.

160 Few microliters of milk samples have been digested with tryp

161 Mean QO2 rates (microliters of O2/cm2 per hour) were: whole cornea, QO2

162 licity of the experimental procedure, use of microliters of organic solvent, short analysis time, sel

163 periments, it is very difficult to add a few microliters of reagent into the solution in an EPR tube

164 method is simple to operate, requires a few microliters of reagent volume, is portable, is reusable,

165 ders of magnitude and requiring only tens of microliters of reagents.

166 uantification take minutes and require a few microliters of sample using only basic laboratory equipm

167 With a few microliters of sample, it is possible to aliquot up to 4

168 s of hours/days, this approach requires only microliters of sample, provides results within minutes,

169 Some microliters of samples were directly dispensed into the

170 tion to handle many samples and requires few microliters of serum samples.

171 tibody specificities with as little as a few microliters of serum specimen.

172 ivity of the method permitted the use of 100 microliters of serum with excellent results.

173 ching a few hundreds nanomolar in only a few microliters of solution.

174 Fifty microliters of the clarified supernatant was then purifi

175 t enables iron quantitation in CSF using 150 microliters of undiluted CSF, sample digestion, dot blot

176 Twenty microliters of whole blood or 10 mul of packed RBCs was

177 ant levels of trypsin activity in only a few microliters of whole blood.

178 Fifteen microliters of Xe were encapsulated into each 1 mg of li

179 m specimens with low concentrations (<1 copy/microliter) of HPV DNA.

180 dialysis report comparing concentrations (pg/microliter) of norepinephrine (NE), serotonin (5-HT) and

181 e relatively large volumes (over one hundred microliters) of blood samples, and therefore, are not su

182 lyzing PFCs in small volumes (less than five microliters) of blood.

183 nts with CD4 cell counts between 119 and 436/microliter on antiretroviral drugs received a single inf

184 th morulae concentration of 282 +/- 48 cells/microliter on day 5 (P = 0.004) and 242 +/- 63 cells/mic

185 er on day 5 (P = 0.004) and 242 +/- 63 cells/microliter on day 8 (P = 0.005).

186 ng neutrophils in blood was 122 +/- 22 cells/microliter on day 8.

187 ntrolled as discrete droplets (picoliters to microliters) on an array of insulated electrodes.

188 d eosinophil count of at least 300 cells per microliter or a sputum eosinophil level of at least 3% w

189 systemic host factors, CD4+ cell counts <200/microliter (OR = 3.0, 95 percent CI 1.3, 6.9) and nucleo

190 ptor agonist clenbuterol (3-3000 pmol in 0.2 microliter) or 8-bromoadenosine 3':5'-cyclic monophospha

191 sttraining intrahippocampal (1 microgram/0.5 microliter) or intracaudate (2 microgram/0.5 microliter)

192 (delta-selective antagonist, 2 micrograms/2 microliters) or nor-binaltorphimine (kappa-selective ant

193 n approximate cell density of five cells per microliter (P < .01).

194 ter) than in 2003-2005 (44+/-169 genomes per microliter, P=0.02), as were parasite densities in place

195 liter) and a recovery in cell number (48 per microliter; p < 0.01) with standard treatment.

196 er of undiluted processed sample DNA to a 50-microliter PCR mixture.

197 When a liquid flow rate in the low microliter per minute range was used, the reconstructed

198 nes and Ag/AgCl electrodes was shown to pump microliter per minute-range flow through a 0.5-mm-diamet

199 nic receptor agonist oxotremorine (10 ng/0.2 microliter per side) or saline.

200 nactivation with lidocaine (10 microgram/0.2 microliter per side), and control rats received buffered

201 ospheric carbon dioxide was increased by 200 microliters per liter in a forest plantation, where comp

202 ) enrichment (ambient concentration plus 200 microliters per liter) in an intact forest.

203 grobacterium tumefaciens, 5% sucrose and 500 microliters per litre of surfactant Silwet L-77.

204 ing at flow rates greater than a few hundred microliters per minute, and providing analysis rates gre

205 e i.c.v. administration of FIVgp120 (5 ng/10 microliter) produces changes in the latency of both cort

206 to reduce sample volumes from milliliters to microliters provides increased clinical utility.

207 Hollow microneedles permitted flow of microliter quantities into skin in vivo, including micro

208 f UV-excited fluorescence from nanoliter and microliter quantities of material, mixed at microsecond

209 f rapid, automated, parallel immunoassays of microliter quantities of samples.

210 Since the reaction volumes are in the microliter range and upscaling of the measurement system

211 ven at low levels, very small samples in the microliter range become accessible for pH-stating: a red

212 ication of DNA at levels in the picogram per microliter range.

213 -free cloning of custom DNA libraries in sub-microliter reaction droplets using programmable digital

214 e preparation, handling, and monitoring of 1-microliter reaction volumes.

215 sed thrombin assays, requiring only minimal (microliter) reagent use.

216 IV) and with CD4 cell counts below 100 cells/microliter received fluconazole daily (200 mg; five pati

217 hind paw, and 24 rats were injected with 50 microliter saline as a control.

218 ABAa agonist, muscimol (0.5 microgram in 0.5 microliter saline), or vehicle was infused into the late

219 asurements with high temporal resolution and microliter sample consumption is presented.

220 the information, allowing the use of minute microliter sample volumes and 100 muM sample concentrati

221 highly precise and sensitive measurements of microliter sample volumes of human blood plasma coagulat

222 ll experiments were carried out using minute microliter sample volumes of lipid vesicle solutions, us

223 Ten-microliter sample volumes reduce reagent consumption and

224 nation against nonhybridized DNA, the use of microliter sample volumes, and disposable transducers an

225 veguide approach not only affords the use of microliter samples but also provides significant improve

226 Now, new technologies using microliter samples of whole blood and exploiting the spe

227 It operates on microliter samples of whole blood, provides positive, co

228 on and detection in a manner that allows for microliter samples to be screened for infectious pathoge

229 Five-microliter samples were injected onto a 4-cm-long by 50-

230 on of proteins at very low concentrations in microliter samples.

231 bsorbance spectroscopy of high absorptivity, microliter samples.

232 de substrates and is readily achievable on a microliter scale (2mul of total volume containing 2mug o

233 hese structures ranges from the nanoliter to microliter scale depending on the number of cycles and c

234 ce designed for electrochemical studies on a microliter scale has been utilized for the examination o

235 ancer cells, and even whole blood on the low microliter scale is suitable for direct PCR amplificatio

236 the silk solutions to be tested rapidly with microliter scale sample sizes.

237 he resulting calcium flux is released into a microliter scale thin layer reservoir, and the resulting

238 pment of miniature MFCs at the milliliter to microliter scale.

239 otein profiles in mouse urine samples at the microliter scale.

240 retching and glass coverslip deposition from microliter-scale DNA samples.

241 When a microliter-scale droplet containing mitochondria is disp

242 Microliter-scale droplet generation, reactant introducti

243 ribes a method for local heating of discrete microliter-scale liquid droplets.

244 rcome the long-standing, stubborn barrier to microliter-scale peak volumes and achieved the highest r

245 rises just four direct reagent additions, in microliter-scale volumes, over the course of a 6-h proce

246 ceiving the lowest dose (0.125 microgram/0.5 microliter/side) demonstrated a robust delayed threshold

247 lpine (0, 0.25, 1.25, and 6.25 microgram/0.5 microliter/side) into one of six brain regions: amygdala

248 CH 23390 at the same dose (0.5 microgram/0.5 microliter/side) resulted in lowered BSR thresholds when

249 f SCH 23390 into the NAcc (0.5 microgram/0.5 microliter/side) were significantly higher than those as

250 tricular (i.c.v.) IL-1ra (500 microgram in 5 microliter) significantly attenuated LPS fever (IL-1ra,

251 The ability to perform kinetics in microliter-size samples makes this methodology particula

252 R enables us to detect ca. 30 parasites in a microliter-sized blood sample, which is the same order o

253 ethods involved characterizing adsorption in microliter-sized droplets by drop tensiometry and in nan

254 olled vibration selectively propels multiple microliter-sized drops along microstructured tracks, lea

255 veraging electrodes with results obtained in microliter-sized hemispherical samples with a source in

256 o support different analytical techniques in microliter-sized samples.

257 emaining six subjects were injected with 5.0 microliters sterile water.

258 pores could be detected when seeded in a 100-microliter stool sample and 10 to 30 C. cayetanensis ooc

259 Ten microliters surfactant were directly applied to the corn

260 ter which nearly all the medium (hundreds of microliters) surrounding the docked and tagged cells was

261 hrough a micropipette attached to a Hamilton microliter syringe.

262 ometric mean [+/-SD], 409+/-1569 genomes per microliter) than in 2003-2005 (44+/-169 genomes per micr

263 ers of magnitude in analyte concentration in microliter to submicroliter volumes of analyte fluid.

264 priate volumes of both samples and reagents (microliters to hundreds of nanoliters) through the syste

265 and precision deteriorate considerably from microliters to nanoliters.

266 ers of magnitude in analyte concentration in microliter-to-submicroliter volumes of analyte fluid.

267 GDNF (10 microgram in 2 microliter vehicle) or vehicle was injected into the rig

268 Microliter-volume ( approximately 2.5 muL) aqueous dropl

269 which ions are extracted from the surface of microliter-volume droplets.

270 stem allows size exclusion chromatography of microliter volumes (termed muL-SEC) to be performed with

271 TH assay and IL-5 assays were carried out on microliter volumes and demonstrated physiologically rele

272 nding in its native serum environment within microliter volumes and without any surface attachments.

273 DNA fragments dissolved in microliter volumes are captured in a nanoliter-sized ban

274 emperature control to accurately thermocycle microliter volumes in microchips fabricated from polyimi

275 The design of our device requires only microliter volumes of affinity chromatography resin-a co

276 counting and can measure levels of (14)C in microliter volumes of biological samples with negligible

277 l without cross-contamination and using only microliter volumes of blood.

278 y ring-down spectroscopy can be performed on microliter volumes of liquids.

279 e acoustic levitation and inherent mixing of microliter volumes of reactants (3 muL droplets), yieldi

280 s developed for reliable application of (sub)microliter volumes of sample without the need of commerc

281 per-based devices wick fluids and distribute microliter volumes of samples from single inlet points i

282 ecovery of model proteins from approximately microliter volumes of serum in a sample-to-answer run ti

283 better than millisecond resolution using sub-microliter volumes of solutions.

284 tical plates/m while generating single digit microliter volumes of waste for a complete chromatograph

285 Samples were deposited in microliter volumes on thin silicon nitride windows and d

286 lation of voltage to volume extending to the microliter volumes that can be handled by digital microf

287 ment took just a few seconds and was done in microliter volumes with nanomolar concentrations of labe

288 peline combines automated sample handling of microliter volumes, temperature and anaerobic control, r

289 Carrying out reactions in very small (microliter) volumes in capillaries has many advantages i

290 a starting concentration of 37.5 copies per microliter was successfully purified from a 10% serum sa

291 Forty microliters was taken for LC/ESI-MS analysis using elect

292 f eNO > 10 ppb and eosinophilia (> 200 cells/microliter) was 90% in predicting airway obstruction (FE

293 ection; a rapid decline in CD4(+) PBMC (<350/microliter) was seen in five of six animals 21 days and

294 e adult skeletal muscle Na+ channel isoform (microliter), we compared the effects on both TTX and STX

295 uding patients with CD4(+) cell counts < 200/microliter weakened this correlation, possibly because o

296 ction volumes ranging from 250 pL to several microliters were made without electrophoretic flow.

297 consumption of drugs was reduced to tens of microliters, which is thousands of times less than tradi

298 ophilia, defined as more than 1500 cells per microliter with end-organ involvement and no recognized

299 me and can detect as low as 200 exosomes per microliter, with a linear range spanning almost 4 orders

300 cal reaction in a microdrop of a few tens of microliters, with a kinetic time resolution of ca. 1 s.