ライフサイエンスコーパス: standard solution

1 pentanol), and donor solution (20 muL sample/standard solution).

2 ere precise and accurate when applied to the standard solution.

3 derivatization and halogenation of the CH3Hg standard solution.

4 0 uL of concentrated HCl for 30 mL of sample/standard solution.

5 en the sample is mixed with the acidic metal standard solution.

6 on is safe in adults and as effective as the standard solution.

7 fully deprotonated chromoionophore), and two standard solutions.

8 ifferent concentrations of these analytes in standard solutions.

9 n to 3 ppb with a linearity up to 400 ppb in standard solutions.

10 -4000 cm(-1) for a set of 50 ternary aqueous standard solutions.

11 nalyte) for calibration rather than on ionic standard solutions.

12 tion of peak identities without the need for standard solutions.

13 ) were measured from each pictures of the TC standard solutions.

14 mmetric aptasensor was used to detect OPN in standard solutions.

15 ke recovery tests and by analyzing synthetic standard solutions.

16 month, limited by consumption of reagent and standard solutions.

17 of 7 polychlorinated biphenyl (PCB) mixture standard solutions.

18 e (<LODs) in these fabric protector original standard solutions.

19 IPY-FL and 500 ymol for tetramethylrhodamine standard solutions.

20 As(III) and 0.08 ppb (S/N = 3) for As(V) in standard solutions.

21 with detection of IgE at amol (pM) levels in standard solutions.

22 Standard solutions (0.05-5mug/mL) were stable for at lea

23 For MC-LR in mixed standard solutions, a linear range of 0.11-5.0 microM (R

24 re constructed and tested using multielement standard solutions, a standard reference material, and a

25 BA levels were determined using an external standard solution added to the sample rotor.

26 used to determine the As(V) concentration in standard solutions after first being chemically reduced

27 ion with monodisperse droplets consisting of standard solutions allowed for the mass quantification o

28 re redispersed in a small volume of internal standard solution and deposited onto a quartz reflector.

29 us parameters affecting the CAP detection in standard solution and in in vitro detection are optimize

30 tool was capable to detect miRNA-29a both in standard solution and in serum, respectively, down to 0.

31 this process and the volumes of the internal standard solution and sample are both fixed by the capil

32 noxy Acetic Acid (2,4-D) herbicide either in standard solution and spiked real samples.

33 differentiated behaviours for AgNP from the standard solution and the meat sample highlighting the r

34 alibration of 30 elements present in a multi-standard solution and then to the analysis of boron, cal

35 Adsorption studies across a 10-REE standard solution and two simulated waste streams demons

36 od can detect melamine as low as 0.01 ppm in standard solutions and 0.5 ppm in real milk samples afte

37 Using purified standard solutions and 1 muL samples of human serum, bot

38 ng polychlorinated biphenyl (PCB) isomers in standard solutions and fish liver samples.

39 determining ascorbic acid concentrations in standard solutions and food supplements, and paracetamol

40 es, has been demonstrated for the laboratory standard solutions and for environmental samples.

41 s demonstrated to capture human insulin from standard solutions and from nuclear extracts of pancreat

42 Mode-independent glucose assays in standard solutions and human serum samples worked reprod

43 Testing with standard solutions and modern lipid-doped sherds confirm

44 nual perturbation by the addition of nitrate standard solutions and natural perturbation by rainfall

45 etic acid, and atrazine at ppb level in both standard solutions and river water sample.

46 method was found to be inaccurate with both standard solutions and samples.

47 For this purpose, both carminic acid aqueous standard solutions and sixteen different commercial beve

48 e clean-up and pre-concentration of 3NT from standard solutions and spiked human urine samples.

49 Elemental standard solutions and SRM soil and tissue digestates we

50 g of acidic, neutral and alkaline stevioside standard solutions and stevia leaves suspensions in wate

51 atterns of degradation, not only between the standard solutions and the beverages, but also from beve

52 ibility with deviations smaller than 1 % for standard solutions and under 4 % for feed samples (80 %

53 re achieved for mu-EME-CE-UV of the drugs in standard solutions and urine samples.

54 internal standard (coming from a conebulized standard solution) and external correction using a matri

55 In general, the standard solutions are highly acidic (e.g., Ga(NO3)3 in

56 rials (SRMs) in the SRM 3180 series of anion standard solutions are reported.

57 oducts for peritoneal dialysis compared with standard solutions are uncertain.

58 carnitine and acetylcarnitine in analytical standard solutions as well as imipramine and desipramine

59 (NIP) was confirmed for CFL, CFD and CFP in standard solutions as well as in milk samples.

60 essure sensor calibrations were performed in standard solutions as well as simulated seawater samples

61 ization of small molecules and peptides from standard solutions, as well as drug spiked human urine.

62 bons (PAHs) and hetero-PAHs (N, S, and O) in standard solutions, as well as three complex PAH-contain

63 amining the mass pattern when conducted on a standard solution at both low and high voltages (+10 V a

64 SPIN source was evaluated by electrospraying standard solutions at 300 nL/min and comparing results w

65 curves is first generated by measurements of standard solutions at different spatial locations in the

66 The potassium estimation in honey and standard solutions (calibration curve) had similar sensi

67 detection limits improved, but dried aqueous standard solutions can be used for external calibration,

68 n despite having little or no activity under standard solution conditions.

69 or endogenous NE was identical to that for a standard solution, confirmed that the oxidation current

70 r the eight different columns was 2.0% for a standard solution containing 1 microg/mL imipramine.

71 hanced sensitivity and reproducibility for a standard solution containing amphetamine, imazalil, and

72 was developed and validated using amino acid standard solutions containing (15)N amino acid isotopolo

73 (2) 50% (v v(-1)) sample plus 50% (v v(-1)) standard solution (containing the analytes).

74 The behaviour of a 40nm AgNPs standard solution during the three digestion steps was a

75 s of the SPR reflectivity curves for several standard solutions (e.g. PBS, HEPES or deionized water).

76 n be achieved when the fraction of the added standard solution (f(std)) is <=0.60 (60%) in the mixtur

77 Interpreter services are a standard solution for addressing language barriers and m

78 method consists first of calibrating a CH3Hg standard solution for delta(13)C CSIA.

79 fects and stability in biological matrix and standard solution for DNSH have been also carried out.

80 esist detachment, even in pH 10.7 ethanol, a standard solution for intentional removal of molecular d

81 er than quinine in 0.05 M sulfuric acid as a standard solution for the determination of luminescence

82 agreed well with the known concentrations in standard solutions for all diffusion layer thicknesses,

83 ionic contents is based on the use of ionic standard solutions for calibration, while the determinat

84 Combining Monte-Carlo simulations with standard solutions for time-inhomogeneous birth-death eq

85 measure ion concentrations by employing one standard solution in conjunction with acid and base and

86 hnique was investigated for PSA detection in standard solution in the concentration range of 3x10 (-8

87 strated analysis of 10 pM digoxin in aqueous standard solutions in 10 min.

88 rameters (agitation, voltage, and time) with standard solutions in formic acid 50 mM.

89 System optimization was performed by using standard solutions; in addition, a very complex sample,

90 reliable only if on-site calibration using a standard solution is performed before ion measurements.

91 The added standard solution is recommended to be the same as the s

92 f NPs, the average signal intensity for each standard solution is typically used, which requires meas

93 When external calibration with standard solutions is done to find the mass of NPs, the

94 m source rock) and the widely used Liquid Os Standard solution (LOsSt).

95 .8%, was obtained on a 30 ng mL(-1)quercetin standard solution (n = 3).

96 erm repeatability on delta(65)Cu for pure Cu standard solutions (NIST SRM 976 and Cu-IPGP), typically

97 Neither the preparation of a series of standard solutions nor the construction of a universal c

98 trated at low field strength (80 MHz) with a standard solution of (13)C-d-glucose and (13)C-l-phenyla

99 ording to a classic recipe and spiked with a standard solution of a PCB congener mixture.

100 The corresponding electropherograms for the standard solution of carnitines at the 1-500 microg/mL l

101 with respect to the peak area of an injected standard solution of glutathione (1 muM) a new quantitat

102 he initial calibration was performed using a standard solution of known linear perfluoroalkyl acids.

103 hemical immunoassay were evaluated using the standard solution of S and N protein in buffer solution

104 hemical immunoassay were evaluated using the standard solution of S-protein in the range of 5.0-500 n

105 g the results of the proposed solver and the standard solution of TFFMFTDECR model through error anal

106 For standard solutions of 2,3,7,8-TCDD, injections of 10 fg

107 The calibration graph obtained for standard solutions of 6-hydroxyluteolin 7-O-glucoside (6

108 pherograms from fmole levels from analytical standard solutions of carnitine and acylcarnitines that

109 MBL-GS muPADs was demonstrated by analyzing standard solutions of ethanol, sulfide, and ammonium.

110 was also evaluated through the injection of standard solutions of four classes of PASHs.

111 Tests have been performed using standard solutions of immunoglobulins and serum samples

112 Standard solutions of known concentration and depth were

113 lution, and reproducibility by analyzing the standard solutions of methyl isobutyl ketone, heptanone,

114 The assay was tested with both standard solutions of nAb as well as human serum samples

115 The direct analysis of standard solutions of several metal salts and human bloo

116 Standard solutions of TAGs containing different ratios o

117 ted with Bradford reagent, it was shown that standard solutions of whey protein were significantly le

118 d at studying the UV-C effects on oleuropein standard solutions once dissolved in ethanol or water.

119 otocols involved the homogeneous spraying of standard solutions onto tissue sections to minimize the

120 ividual antioxidant capacity of compounds in standard solutions or complex mixtures.

121 Acyl CoA esters from standard solutions or plant extracts were derived to the

122 Coupled to more standard solution phase enrichment techniques, it would

123 employed as versatile intermediates for both standard solution-phase and solid-phase synthetic transf

124 NBS28 Si standard solutions prepared in nutrient-free seawater an

125 is (DSS-EA) were optimized and calibrated by standard solutions, rather than by certified reference m

126 rements of 0.15 mug mL(-1) Se(IV) and Se(VI) standard solution, respectively.

127 n variations of 3.2% and 0.5% for beer and a standard solution, respectively.

128 -110%) and mavacoxib (F% = 111-113%), CF and standard solutions, respectively.

129 pH(i) in the standard solutions showed a slow acidification over at l

130 In addition to standard solutions, this method was used on rice samples

131 The standard solution to this problem is to limit the studie

132 activity determined from (242)Pu and (243)Am standard solutions, to correct for residual (241)PuO(+)

133 high retained dislocation density, prior to standard solution treatment and aging.

134 under wet plasma conditions where a thallium standard solution was introduced to the mass spectromete

135 Stability of working standard solutions was also examined.

136 Using HeLa tryptic digested standard solutions, we demonstrate preferential adsorpti

137 Signals from standard solutions were fit to a logistic equation, allo

138 on factors requires additional twists to the standard solution, which are beginning to become apparen

139 erage and enabled external calibration using standard solutions, which provided accurate results for

140 present in commercially available samples or standard solutions, which was monitored by means of cycl

141 measured after the subsequent addition of a standard solution with known concentration.

142 rinciple behind this scheme is that adding a standard solution with the certified isotope ratio decre

143 out in all chemistry laboratories-to prepare standard solutions with different concentrations for ass

144 in vulnerability analyses, where the use of standard solutions with high gamma overestimates hydraul