ライフサイエンスコーパス: calibration standard

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

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

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

4 mained unaltered between sample extracts and calibration standards.

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

6 ify CPs using technical mixtures as external calibration standards.

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

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

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

10 primary analytical methods in the absence of calibration standards.

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

12 in laboratory sample preparation methods and calibration standards.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

29 Criteria for a calibration standard are proposed.

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

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

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

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

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

35 Calibration standards containing dA and fortified with r

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

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

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

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

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

41 Preparation of calibration standards for cell enumeration is critical i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 Six cellulase calibration standards were prepared using affinity diges

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

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

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

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

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