ライフサイエンスコーパス: calibration standard

1 nst the known spiked-in ratios (CVs < 8% for calibration standards).

2 d solvents, which can be used as an internal calibration standard.

3 e/Xe, Ar/Xe, and Kr/Xe using air as the only calibration standard.

4 ter for all gas ratios using air as the only calibration standard.

5 a A, human STATHERIN, and an artificial SARS calibration standard.

6 applied at low temperature using inexpensive calibration standards.

7 mained unaltered between sample extracts and calibration standards.

8 tration requires the use of single-homologue calibration standards.

9 ify CPs using technical mixtures as external calibration standards.

10 s, it is essential to have accurate, stable, calibration standards.

11 nd researchers, it is essential to have good calibration standards.

12 nd researchers, it is essential to have good calibration standards.

13 primary analytical methods in the absence of calibration standards.

14 tios without the use of internal or external calibration standards.

15 n inbred strains can often be relied upon as calibration standards.

16 in laboratory sample preparation methods and calibration standards.

17 calculating compound concentrations based on calibration standards.

18 ents in electrical circuits and systems, and calibration standards.

19 o generate distinct rye isolates to serve as calibration standards.

20 in DESI-MSI without an infusion of exogenous calibration standards.

21 sides the reciprocal of the variance of each calibration standard (1/s(i)(2)), more empirical weighti

22 Since these peptides are used as calibration standards, accurate and precise measurement

23 better than those observed for the external calibration, standard additions, and internal standard m

24 ded to final sample extracts and matrix-free calibration standards alike, these analyte protectants i

25 h the binding site inactivated and eGFP as a calibration standard among laboratories and cell types.

26 -pulse measurements without using a particle calibration standard and by approximating the noncylindr

27 Due to the availability of the calibration standard and the large dynamic range of our

28 as programmed such that the LHS diluted both calibration standards and a test sample multiple times w

29 Purified buffalo proteins were used as calibration standards and a total of 536 individual milk

30 Six different methods for applying calibration standards and an internal standard were eval

31 , should be ideal for characterizing primary calibration standards and certified reference materials

32 nalyze approximately 20 specimens, including calibration standards and controls, with all measurement

33 ication approach was based on 10 elements as calibration standards and provided the determination of

34 plate is considered a typical "tray" having calibration standards and quality control (QC) samples d

35 DESI-MS/MS method was evaluated by preparing calibration standards and quality control (QC) samples o

36 The throughput, including calibration standards and quality control samples, is ap

37 d out by two independent laboratories, using calibration standards and real breath samples from healt

38 Here, an algorithm to assure that calibration standards and samples meet the assumption of

39 S) that can be reliably measured across both calibration standards and samples.

40 te that elimination of kinetic outliers from calibration standards and test samples improves the accu

41 y between 0 and 25 ng/mL and both the plasma calibration standards and the plasma samples were stable

42 ccuracy achieved in analysis of five nonzero calibration standards and three quality control standard

43 Consequently, matrix-matched calibration standards and using isotopically labeled (IL

44 ining 5 mg L(-1) Na, K, Ca, Mg added both to calibration standards and water samples.

45 Criteria for a calibration standard are proposed.

46 On-chip/on-petri dish nanoscale capacitance calibration standards are used to quantify the electroni

47 d for absolute quantification if appropriate calibration standards are used.

48 ysis of high-mass proteins requires suitable calibration standards at high m/z ratios.

49 DOSCATs (DOuble Standard conCATamers), novel calibration standards based on QconCAT technology, to un

50 n general, required that additional transfer calibration standards be used.

51 ces the space needed on the MALDI slides for calibration standards by approximately 80%.

52 ons could be quantified without the need for calibration standards by measuring the millimolar proton

53 brane protein complexes, higher mass soluble calibration standards consistently yield more accurate O

54 Calibration standards containing dA and fortified with r

55 pproach was adopted to prepare gelatin-based calibration standards containing the SERS nanotags, whic

56 tation function that automatically generates calibration standard curves from series of standards tha

57 s sample substrates that provide an internal calibration standard during Raman measurements.

58 biases, a novel approach, using FFPE-treated calibration standards, enabled accurate and precise quan

59 on models, which significantly decreased the calibration standard error from 0.50 to 0.03log10 (cells

60 Using a calibration standard fabricated in our lab to test our p

61 We showed that applying a dilution series of calibration standards followed by a homogeneously applie

62 the use of an enriched isoform solution as a calibration standard for absolute quantification studies

63 urfaces can be utilized as a stable internal calibration standard for reproducible quantitative measu

64 ted as the preparation of highly multiplexed calibration standards for bioimaging applications by LA-

65 Preparation of calibration standards for cell enumeration is critical i

66 using individual discrete mass oligomers as calibration standards for GPC.

67 3 and T = 4 capsids makes them attractive as calibration standards for resistive-pulse sensing becaus

68 These fibre-FISH samples provided accurate calibration standards for the entire panel and led to de

69 tive PCR assay utilizes a synthetic internal calibration standard (ICS) that contains priming sequenc

70 For calibration standards, IMPA and PMPA gave a linear respo

71 We also investigate how the common use of a calibration standard in nuclear magnetic resonance (NMR)

72 rious biological matrixes was achieved using calibration standards in plasma, largely improving effic

73 times that differ considerably from those of calibration standards in pure solvents.

74 comprehensive, inexpensive, and memory-free calibration standards is of particular interest to the m

75 available endogenous analytes as a source of calibration standards makes our standard addition-based

76 haracterization of a high-density microarray calibration standard, manufactured in-house and designed

77 protein, which can subsequently serve as the calibration standard of anti-SARS-CoV-2 S1 IgG in serolo

78 as been hindered by the absence of traceable calibration standards of known (41)Ca activity concentra

79 ns were accounted for by imaging fluorescent calibration standards on a daily basis.

80 microscope slides containing either gelatin calibration standards or Eu- and Ho-tagged cell samples.

81 ble using APCI, allowing quantification with calibration standards prepared in solvent.

82 characterized for quantitative imaging using calibration standards, similar calibration tools for imm

83 W) and NIST values based on their respective calibration standards suites is within 0.05%, 0.13%, and

84 were measured 10-fold and bracketed with two calibration standards that covered a wide range of delta

85 d by the difficulty of preparing appropriate calibration standards that relate measured fluorescence

86 T = 4 HBV capsids were calculated without a calibration standard to be 25.2 +/- 0.3 and 28.1 +/- 0.3

87 terized, one of the capsids can be used as a calibration standard to determine the effective diameter

88 Ubiquitin was used as an internal mass calibration standard to measure the molecular mass of cy

89 We used differentiated calibration standards to generate quantitative data for

90 proves the accuracy within the limits of the calibration standards used to characterize the distribut

91 the discrete mass oligomers as internal and calibration standards was demonstrated.

92 As a calibration standard, we have measured XMCD and X-ray ab

93 Using nuclear pores as an internal calibration standard, we show that the dynein comet cons

94 termined from five measurements of the mixed calibration standard were 3.3, 5.3, and 5.4%, respective

95 The calibration standards were analyzed by SERS mapping, and

96 all tissue sections for normalization, while calibration standards were applied in a quantitative man

97 Consequently, matrix-matched calibration standards were employed to determine analyte

98 Samples and calibration standards were prepared in Tris buffer (pH:7

99 Six cellulase calibration standards were prepared using affinity diges

100 Matrix matched calibration standards were used to improve the percent r

101 ation (slope 1.05, r(2) 0.9257); independent calibration standards were used.

102 icroparticles concentration in solution, two calibration standards were used: Virus-Like Particles (V

103 ecoveries of the method, established against calibration standards, were 91-121% and 90-113% (without

104 s possible down to contents of ~100 ag using calibration standards which were produced using the same

105 ng-wave ion mobility data through the use of calibration standards with similar masses and mobilities

106 rom the sample of interest without premixing calibration standards with the analytes.