ライフサイエンスコーパス: microanalysis

1 cording to quantitative x-ray electron probe microanalysis.

2 atomic force microscopy, and X-ray elemental microanalysis.

3 logical Standard Glasses (CGSG) designed for microanalysis.

4 to in quantities sufficient for disaccharide microanalysis.

5 ers were compared using electron probe x-ray microanalysis.

6 e characterized by GC-MS, FT-NMR, FT-IR, and microanalysis.

7 R ((1)H and (31)P) spectroscopy, ESI-MS, and microanalysis.

8 optical computing, information storage, and microanalysis.

9 escence spectroscopy, mass spectrometry, and microanalysis.

10 he optical exploration of microchemistry and microanalysis.

11 the chip using electrophoretically mediated microanalysis.

12 endinosus muscles using electron probe x-ray microanalysis.

13 This identification was confirmed by x-ray microanalysis.

14 aining organelles detected by electron probe microanalysis.

15 zing, ultracryomicrotomy, and electron probe microanalysis.

16 own in high salt medium as detected by x-ray microanalysis and plasma emission spectrometry.

17 plications in a variety of fields, including microanalysis and single-cell analysis, where the amount

18 Electron probe X-ray microanalysis and X-ray diffraction revealed that the ch

19 aracterized using electron microscopy, x-ray microanalysis, and enzymatic markers, and it was demonst

20 sing transmission electron microscopy, x-ray microanalysis, and immunofluorescence microscopy.

21 ergy-dispersive spectroscopy, electron probe microanalysis, and laser ablation inductively coupled pl

22 We adapted a microanalysis approach, using laser ablation inductively

23 identified by electron microscopy and X-ray microanalysis as acidocalcisomes (electron-dense vacuole

24 oles identified morphologically and by X-ray microanalysis as the acidocalcisomes.

25 X-ray microanalysis at two positions behind the apex determine

26 ll is individually addressable and acts as a microanalysis chamber where sample solution passes throu

27 mbined with energy-dispersive electron probe microanalysis (EDX), transmission electron microscopy (T

28 (TEM) combined with energy-dispersive X-ray microanalysis (EDX).

29 gnesium, and calcium, as determined by x-ray microanalysis, either in situ or when purified using iod

30 apillaries with electrophoretically mediated microanalysis (EMMA) at both the ensemble and the single

31 this work, quantitative electron probe X-ray microanalysis (EPMA) and Raman microspectrometry (RMS) w

32 ity of thin films by means of electron probe microanalysis (EPMA) either by wavelength-dispersive X-r

33 cle was determined with electron probe x-ray microanalysis (EPMA) of rapidly frozen papillary muscles

34 uoride profiles determined by electron probe microanalysis (EPMA) supported PLM and MRG findings.

35 (SEM), wavelength-dispersive electron probe microanalysis (EPMA), electron backscattered diffraction

36 oduced the technique of electron probe X-ray microanalysis (EPMA), yet the community remains unable t

37 We used electron probe x-ray microanalysis (EPXMA) to simultaneously examine concentr

38 ents combined with state-of-the-art electron microanalysis (focused ion beam and aberration-corrected

39 ransmission electron microscopic (TEM) x-ray microanalysis for elemental composition, fluoride analys

40 Single-cell bioanalytical microanalysis has also become increasingly valuable for

41 acellular potassium (by electron probe x-ray microanalysis, K+ peak-to-background ratio 0.95+/-0.32 v

42 een fully characterized by NMR spectroscopy, microanalysis, mass spectrometry, and X-ray crystal stru

43 acellular K+ content by electron probe x-ray microanalysis (n=6).

44 Quantitative energy-dispersive x-ray microanalysis of cryosections from hippocampal slice cul

45 Electron probe microanalysis of cryosections from rapidly frozen slice

46 A microanalysis of hunger-driven and palatability-driven f

47 ith LA-ICP-MS as an alternative strategy for microanalysis of immunohistochemical sections.

48 esolved in part through the use of selective microanalysis of individual wood cells.

49 X-ray elemental microanalysis of particles showed that Cl/Na ratio decre

50 we describe several methods for quantitative microanalysis of peptides in individual Aplysia californ

51 concentration ([Ca](mito)) obtained by x-ray microanalysis of rapidly frozen neurons from frog sympat

52 s in different cell types were quantified by microanalysis of single-cell samples and phloem exudates

53 X-ray microanalysis of the electron-dense vacuoles or polyphos

54 X-ray microanalysis of the volutin granules showed large amoun

55 The proposed nanoassay may be applied in microanalysis of trace amounts of proteins, e.g. in micr

56 l UV-vis sensing method for enantioselective microanalysis of unprotected amino acids, amines, amino

57 The proposed model based on the atomic force microanalysis suggests that this tailoring leads to unif

58 y with on-chip assay elements would create a microanalysis system for point-of-care diagnostics, redu

59 -alone cytometers or as a part of integrated microanalysis systems.

60 tropically etched profiles often employed in microanalysis systems.

61 Several single cell microanalysis techniques have been developed but tend to

62 is strong evidence, obtainable only through microanalysis, that secondary materials used in the devi

63 alysis of enrollment are consistent with the microanalysis: the argan boom seems to have improved edu

64 scanning electron microscopy (SEM) and x-ray microanalysis, these granulocytes contain calcium carbon

65 s that were shown by energy-dispersive x-ray microanalysis to be mainly in epidermal cells.

66 apillary to support electrophoresis mediated microanalysis using neuraminidase to analyze sialic acid

67 Microanalysis was performed using a capillary liquid chr

68 Thus, electron probe X-ray microanalysis was used to determine the effects of post-

69 Electron probe microanalysis was used to determine the total (free+boun

70 Electron probe x-ray microanalysis was used to measure percentage water and c

71 ith that of 7.6(7) found from an X-ray Pt/Pd microanalysis (WDS spectrometer) on three crystals of 1.

72 ctron microscopy and energy dispersive X-ray microanalysis were consistent with elongated prismatic c

73 ug-plug mode of electrophoretically mediated microanalysis, with nanolitre injected volumes of enzyme

74 y its conversion back to (Ph3P)6Cu6H6 and by microanalysis; X-ray diffraction shows that the complex