ライフサイエンスコーパス: FT-ICR-MS

1 FT-ICR MS was used to locate the labeled carbon distribu

2 n cyclotron resonance mass spectrometry (21T FT-ICR MS).

3 2D FT-ICR MS allows the correlation between precursor and f

4 2D FT-ICR MS has been optimized as a data-independent metho

5 we used electron capture dissociation for 2D FT-ICR MS for the first time, and we recorded two-dimens

6 In the present study, the capabilities of 2D FT-ICR MS are explored with a tryptic digest of cytochro

7 on cyclotron resonance mass spectrometry (2D FT-ICR MS) allows the correlation between precursor and

8 resolution FT-ICR MS/MS analysis, but the 2D FT-ICR MS method required only one experimental scan.

9 high mass resolving power single-acquisition FT-ICR-MS analysis of peptides and proteins ranging from

10 cyclotron resonance mass spectrometry (APPI FT-ICR MS) to identify molecular transformations in oil-

11 the overall loss of HMW species observed by FT-ICR MS has not previously been documented and is coun

12 g unique advantages of SID over conventional FT-ICR MS ion activation techniques for structural chara

13 lyses of O-linked glycans from mucin by DESI-FT-ICR-MS and matrix-assisted laser desorption/ionizatio

14 cyclotron resonance mass spectrometry (DESI-FT-ICR-MS) for the analysis of carbohydrates.

15 We demonstrate how 2D ECD FT-ICR MS can be implemented to identify peptides and gl

16 e the sequence coverage obtained with 2D ECD FT-ICR MS with the sequence coverage obtained with ECD M

17 The mass spectra acquired by ESI FT-ICR MS of untreated, borohydride-reduced, and borodeu

18 7-41% of the DOM molecules identified by ESI FT-ICR MS, may suggest a microbial provenance and high b

19 yclotron resonance mass spectrometry (LC ESI FT-ICR MS) to determine the sugar composition, linkage p

20 yclotron resonance mass spectrometry (LC ESI FT-ICR MS).

21 cyclotron resonance mass spectrometry (ESI(-)FT-ICR MS) and physicochemical characterisation analysis

22 ESI(-)-FT-ICR MS is a powerful tool to predict the physicochemi

23 The ESI-FT-ICR MS readings were acquired and the data were corre

24 the solid-phase extraction procedure and ESI-FT-ICR-MS which allowed precise evaluation of the DOM mo

25 nd (31)P), mass spectrometry (ESI-MS and ESI-FT-ICR-MS), and elemental analysis.

26 n cyclotron resonance mass spectrometry (ESI-FT-ICR-MS) and IR analysis of the isolated cofactor and

27 n cyclotron resonance mass spectrometry (ESI-FT-ICR-MS).

28 n Cyclotron Resonance Mass Spectrometry (ESI-FT-ICR-MS).

29 bserved, as the number of peaks from the ESI-FT-ICR-MS spectra decreased.

30 demonstrates significant advantages of FI/FD FT-ICR MS for analysis of nonpolar molecules in complex

31 uture generation of ultrahigh magnetic field FT-ICR MS equipped with harmonized ICR cells.

32 high H/C values of identified formulas from FT-ICR MS data.

33 Metabolic fingerprints from FT-ICR-MS data could discriminate wines according to the

34 ARAFAC)) and the exact mass information from FT-ICR-MS, and thus revealing the extent of sulfur-conta

35 Furthermore, FT-ICR MS detection consistently demonstrated good mass

36 o ultrahigh resolution mass analyzers (e.g., FT-ICR MS).

37 Comparison between acquired data from the GC/FT-ICR MS (in broadband mode) and a commercial GC quadru

38 range) indicates that sensitivity of the GC/FT-ICR MS is an order of magnitude lower.

39 andem MS capabilities afforded by the hybrid FT-ICR-MS platform.

40 enerated ions by collisions with surfaces in FT-ICR MS is a new powerful method for characterization

41 quency multiples for increased throughput in FT-ICR MS, essential for numerous applications with time

42 sed detection limit should become routine in FT-ICR-MS data processing.

43 290 fmol/ml) nano-LC-electrospray ionization-FT-ICR-MS data did not reveal any endogenous BNP-32.

44 SI infrared multiphoton dissociation (IRMPD) FT-ICR MS yields mostly b and y fragment ions for each p

45 Nano-LC FT-ICR MS and quadrupole linear ion trap MS/MS analysis

46 C/ESI-Q-TOF MS and intact CHH analysis by LC/FT-ICR-MS.

47 n cyclotron resonance mass spectrometry (LTQ FT-ICR MS) to simultaneously measure the isotopic enrich

48 ear to be effective in the analysis of MALDI FT-ICR MS data.

49 cyclotron resonance mass spectrometry (MALDI FT-ICR MS).

50 ibrinogen further demonstrated that AP MALDI-FT ICR MS is ideal for the study of complex glycan sampl

51 cyclotron resonance mass spectrometry (MALDI-FT-ICR MS) and single cell imaging flow cytometry to det

52 e, including direct tissue analysis by MALDI-FT-ICR-MS, de novo sequencing of tryptic digested CHH by

53 f CHH in the direct tissue analysis by MALDI-FT-ICR-MS.

54 ourier transform ion cyclotron resonance MS (FT-ICR MS) demonstrated that the mass accuracy of the Or

55 an optimized strategy for wide-scan DI nESI FT-ICR MS that increases dynamic range but maintains hig

56 clotron resonance mass spectrometry (DI nESI FT-ICR MS) offers high mass accuracy and resolution for

57 rrelate with DOM composition, the ability of FT-ICR MS to characterize DOM subpopulations provides un

58 resolution and mass measurement accuracy of FT-ICR MS can be utilized for unambiguous molecular form

59 gh mass resolving power and mass accuracy of FT-ICR MS enable definitive elemental composition assign

60 the relatively low data acquisition rate of FT-ICR MS.

61 ed worldwide to quantify BNP-32 from plasma, FT-ICR-MS (unprecedented mass measurement accuracy) coup

62 ability and precision as the high resolution FT-ICR MS.

63 ost matched data provided by high-resolution FT-ICR MS/MS analysis, but the 2D FT-ICR MS method requi

64 ing power of 90-220) to ultrahigh resolution FT-ICR MS (resolving power over 400k) permitted the iden

65 nsform Ion Cyclotron Resonance mass spectra (FT-ICR-MS) of natural organic matter are complex and con

66 m ion cyclotron resonance mass spectrometer (FT-ICR MS) are described.

67 m Ion Cyclotron Resonance Mass Spectrometer (FT-ICR MS) specially configured for SID experiments.

68 m ion cyclotron resonance mass spectrometer (FT-ICR MS) specially configured for surface-induced diss

69 m ion cyclotron resonance mass spectrometer (FT-ICR MS) specially designed for studying interactions

70 m ion cyclotron resonance mass spectrometer (FT-ICR MS) specially equipped to perform SID experiments

71 m ion cyclotron resonance mass spectrometer (FT-ICR MS) specially equipped to perform SID experiments

72 0 T Fourier transform ICR mass spectrometer (FT-ICR MS).

73 ion cyclotron resonance mass spectrometers (FT-ICR-MS).

74 m ion cyclotron resonance mass spectrometry (FT ICR MS) under UV laser and solid matrix conditions ha

75 m ion cyclotron resonance mass spectrometry (FT ICR MS), can resolve thousands of molecular ions in c

76 m ion cyclotron resonance mass spectrometry (FT-ICR MS) and ion trap tandem mass spectrometry.

77 m-ion cyclotron resonance mass spectrometry (FT-ICR MS) and quantify DOM photochemical activity using

78 and ultrahigh resolution mass spectrometry (FT-ICR MS) enables an improved characterization of compl

79 m ion cyclotron resonance mass spectrometry (FT-ICR MS) for direct separation and characterization of

80 m-ion cyclotron resonance mass spectrometry (FT-ICR MS) indicate the lack of an oxidatively functiona

81 m ion cyclotron resonance mass spectrometry (FT-ICR MS) is applied to the analysis of the low energy

82 m ion cyclotron resonance mass spectrometry (FT-ICR MS) provides ultrahigh resolution and ultrahigh m

83 m ion cyclotron resonance mass spectrometry (FT-ICR MS) technique to characterise in situ chemical co

84 m ion cyclotron resonance mass spectrometry (FT-ICR MS) to determine the elemental compositions of DO

85 m ion cyclotron resonance mass spectrometry (FT-ICR MS) typically utilizes an m/z-independent excitat

86 m ion cyclotron resonance mass spectrometry (FT-ICR MS), due to the relatively low data acquisition r

87 m ion cyclotron resonance mass spectrometry (FT-ICR MS).

88 m ion cyclotron resonance mass spectrometry (FT-ICR MS).

89 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) "top-down" analysis of PA1006 purified from P

90 d by ultrahigh resolution mass spectrometry (FT-ICR-MS) and excitation emission matrix fluorescence (

91 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) and time-of-flight mass spectrometry (TOF-MS)

92 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) as a nontargeted technique to assign unambigu

93 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) for the analysis of a pyrolysis liquid from b

94 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) has rapidly established a prominent role in p

95 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) identified both the photolabile and the photo

96 PPI) ultrahigh resolution mass spectrometry (FT-ICR-MS) revealed a strong interaction between DOM and

97 m ion cyclotron resonance mass spectrometry (FT-ICR-MS) to determine the biodegradability and molecul

98 m ion cyclotron resonance mass spectrometry (FT-ICR-MS), combined with chromatographic prefractionati

99 m-Ion Cyclotron Resonance-Mass Spectrometry (FT-ICR-MS), which delivered the molecular formulae and i

100 m ion cyclotron resonance mass spectrometry (FT-ICR-MS).

101 m ion cyclotron resonance mass spectrometry (FT-ICR-MS).

102 and ultrahigh-resolution mass spectrometry (FT-ICR-MS).

103 e 4 times higher than those provided by 10 T FT-ICR MS with a standard ICR cell.

104 sample from the deep North Pacific on a 15 T FT-ICR-MS; each of these replicate runs consisted of 500

105 ays in D. vulgaris and also demonstrate that FT-ICR MS is a powerful tool for isotopomer analysis, ov

106 The FT-ICR MS instrument includes a liquid injection field d

107 The FT-ICR MS/MS techniques of electron capture dissociation

108 limited by the slow acquisition rate of the FT-ICR MS (<1 Hz), a database driven retention time comp

109 rinciple for further application of OSA-TIMS-FT-ICR MS for the unsupervised analysis of complex mixtu

110 ections (<1%) can be measured using OSA-TIMS-FT-ICR MS with high mobility resolving powers (RIMS up t

111 In the case of OSA-TIMS-FT-ICR MS, the TIMS operation sequence, trapping conditi

112 ide 3 KRGRGRPRK [M + 2H](+2) during OSA-TIMS-FT-ICR MS.

113 The TIMS-FT-ICR MS analysis provided, in addition to the heteroat

114 Insights generated using FT-ICR-MS analysis can be confirmed and further explored

115 n a glycosylation site-specific manner using FT-ICR-MS and Edman sequencing.

116 and transient isotachophoresis, coupled with FT-ICR MS to improve the overall detection of cationic m

117 earing organic formulas were identified with FT-ICR-MS in the stormwater runoff and pond outflow wate

118 nd the level of identification possible with FT-ICR-MS.