ライフサイエンスコーパス: standard solution

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

2 derivatization and halogenation of the CH3Hg standard solution.

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

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

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

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

7 ke recovery tests and by analyzing synthetic standard solutions.

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

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

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

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

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

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

14 fully deprotonated chromoionophore), and two standard solutions.

15 ifferent concentrations of these analytes in standard solutions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

34 Elemental standard solutions and SRM soil and tissue digestates we

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 Standard solutions of known concentration and depth were

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

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

77 Standard solutions of TAGs containing different ratios o

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

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

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

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

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

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

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

85 -110%) and mavacoxib (F% = 111-113%), CF and standard solutions, respectively.

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

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

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

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

90 Stability of working standard solutions was also examined.

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

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

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

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

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