ライフサイエンスコーパス: gas chromatograph

1 d fused silica capillary to an injector of a gas chromatograph.

2 an analytical instrument such as a liquid or gas chromatograph.

3 cetamide (BSTFA) prior to injection into the gas chromatograph.

4 4)C-labeled compounds were injected into the gas chromatograph.

5 ith a photoionization source interfaced to a gas chromatograph.

6 utput of a thermionic detector attached to a gas chromatograph.

7 n be introduced into the injection port of a gas chromatograph.

8 ucted with the detector interfaced to a fast gas chromatograph.

9 eathing air through an injection port from a gas chromatograph.

10 he PIES detector was set up in series with a gas chromatograph and a thermal conductivity detector.

11 A gas chromatograph and combustion and reduction furnaces

12 inogen synthesis and degradation rates using gas chromatograph and mass spectrometry analysis.

13 pentane are first separated using a standard gas chromatograph and then introduced into a MCA flow ce

14 uction under visible light were evaluated by gas chromatograph, and the midgap states of ZnS introduc

15 ntration system for use with continuous-flow gas chromatograph combustion isotope ratio mass spectrom

16 A gas chromatograph-combustion (GC-C) system is described

17 lend was performed through a two-dimensional gas chromatograph coupled to a mass spectrometer with ti

18 ction in isooctane, and then injected into a gas chromatograph coupled to a multicollector inductivel

19 (DEHP) in packaged food prior to analysis by gas chromatograph coupled with flame ionisation detector

20 oncentrations determined by biosensor and by gas chromatograph coupled with mass spectrometer exhibit

21 A portable ultra-fast gas-chromatograph coupled with a surface acoustic wave s

22 PRBS) with a mean frequency of 0.1 Hz into a gas chromatograph equipped with a flame ionization detec

23 at 230 degrees C in the injection port of a gas chromatograph equipped with a flame ionization detec

24 e remaining gas species are analyzed using a gas chromatograph equipped with a mass spectrometer (GC-

25 is quantified in the organic extract using a gas chromatograph equipped with both a short-path therma

26 ry columns housed in a standard Agilent 6890 gas chromatograph fitted with a high data acquisition ra

27 Samples are injected into a gas chromatograph fitted with a megabore capillary colum

28 L of the sedimented phase was analysed using gas chromatograph-flame ionisation detector (GC-FID) and

29 hermally desorbed in the injection port of a gas chromatograph for separation, detection, and quantit

30 the utility of a relatively simple multiplex gas chromatograph for the analysis of environmental samp

31 transient ion source, it was connected to a gas chromatograph for the mass spectrometric determinati

32 plasma (LTP) ionization interface between a gas chromatograph (GC) and an atmospheric pressure inlet

33 The method uses a gas chromatograph (GC) coupled with a multicollector ind

34 A prototype gas chromatograph (GC) electron monochromator (EM) refle

35 The nitrobenzene produced was measured on a gas chromatograph (GC) equipped with a nitrogen-phosphor

36 beads, followed by loading the beads into a gas chromatograph (GC) injector insert for subsequent de

37 rface (CRI) to convert samples coming from a gas chromatograph (GC) or high-performance liquid chroma

38 A small, portable gas chromatograph (GC) was assembled for the trace detec

39 opment of a comprehensive, three-dimensional gas chromatograph (GC3) instrument is described.

40 A gas chromatograph has been coupled to a direct-current g

41 A novel comprehensive two-dimensional gas chromatograph has been developed that utilizes diffe

42 Gas chromatographs have been flown to both Mars and Venu

43 etic isotope effects were determined using a gas chromatograph in conjunction with a mass selective d

44 nventional extractives, known androgens, and gas chromatograph index (GCI) profiles.

45 The gas chromatograph-ion mobility spectrometer (GC-IMS) has

46 scribed technique in which the effluent of a gas chromatograph is continuously analysed isotopically,

47 Effluent from the gas chromatograph is pyrolyzed by passage over a heated

48 s for analysis of trace components in air, a gas chromatograph isotope ratio mass spectrometer (GC-IR

49 Coupled to a gas chromatograph, labeling analysis provided enrichment

50 ort direct atmospheric measurements from the Gas Chromatograph Mass Spectrometer (GCMS), including al

51 ctosamine (GalNAc), and glucose (Glc), using gas chromatograph mass spectrometry (GC-MS), matrix-assi

52 rometry (AMS) instrument with a conventional gas chromatograph-mass spectrometer (GC/MS) is described

53 thyl esterificated with BF3, and analyzed by gas chromatograph-mass spectrometer (GC/MS).

54 with a cooled injection system coupled to a gas chromatograph-mass spectrometer (ILR-CIS-GC-MS) has

55 through extraction with dichloromethane and gas chromatograph-mass spectrometer analysis.

56 We measured retinoid levels by gas chromatograph-mass spectrometer technique in plasma

57 tomated fashion and injected directly into a gas chromatograph-mass spectrometer without further work

58 et al. claims to show that the Viking GCMS (gas chromatograph-mass spectrometer) experiment, which c

59 formance liquid chromatography, 15N NMR, and gas chromatograph-mass spectrometry analyses.

60 obtained by solid-phase microextraction and gas chromatograph-mass spectrometry were analysed using

61 lipid molecular species are determined with gas chromatograph-mass spectrometry.

62 tates continuous admission of analyte into a gas chromatograph/mass spectrometer (GC/MS) for methods

63 A prototype microfabricated gas chromatograph (muGC) adapted specifically for the ra

64 s of two identical prototype microfabricated gas chromatographs (muGC) adapted for the in situ determ

65 the use of two prototype Si-microfabricated gas chromatographs (muGC) for continuous, short-term mea

66 (GC-FID) and the peaks were confirmed using gas chromatograph-positive chemical ionisation-mass spec

67 ages of PBDDs and PXDDs were studied using a gas chromatograph-quadrupole time-of-flight (GC-QTOF) ma

68 ogate compounds, which are assigned based on gas-chromatograph retention time and mass spectral signa

69 es must be volatile enough to pass through a gas chromatograph, silylated derivatization reactions ar

70 s of selected parameters calculated from the gas chromatograph spectra are in a remarkable narrow ran

71 he ability of the thermal desorption aerosol gas chromatograph (TAG) to measure gas-to-particle-phase

72 system programmable-temperature vaporization gas chromatograph (TDS-PTV-GC) with a mu-ECD detector.

73 A prototype portable gas chromatograph that combines a multiadsorbent preconc

74 mperature-programmable silicon micromachined gas chromatograph that employs a standard capillary colu

75 fraction is automatically transferred to the gas chromatograph to be analysed.

76 ned plasma chip is coupled to a conventional gas chromatograph to investigate its performance as an o

77 Details of interfacing a high-pressure gas chromatograph to the internal ion source of a Fourie

78 A modest gas chromatograph which uses air as the carrier gas was

79 simple coupling of a standard, packed-column gas chromatograph with a microcantilever array (MCA) is

80 nsitivity and precision when combined with a gas chromatograph with barrier ionization discharge (GC-

81 em quadrupole mass spectrometer coupled to a gas chromatograph with headspace autosampler (HS-GC-MS/M

82 anometalloidal compounds were detected using gas chromatograph with mass spectrometric or fluorine-in