ライフサイエンスコーパス: CLSM

1 CLSM analyses revealed that "high biofilm forming" (HBF)

2 CLSM and MPLSM showed that L-FABP expression enhanced by

3 CLSM observations corroborated the SS-OCT findings.

4 emporal dependence of sample excitation in a CLSM, there is no need for a pulsed or modulated light s

5 fluorescence microscopy (epifluorescence and CLSM imaging with DNA, RNA, EPS, and protein and lipid s

6 ght-field and epifluorescence microscopy and CLSM showed that biofilm development (observed until 24

7 NMR and CLSM analysis support the interactions between polypheno

8 The cryo-SEM and CLSM micrographs showed that minimum porosity was observ

9 The cryo-SEM and CLSM techniques were used to observe the microstructure

10 ed by comparing fiber diameters from SEM and CLSM to be between 0.46% to 3.8% of the SEM reference va

11 Mapping the fluorescence intensity in 3D by CLSM enables us to reconstruct the relative concentratio

12 omogeneous biofilm coating, as determined by CLSM, and a near uniform distribution of biomass and bio

13 imental fluorescence profiles, determined by CLSM, have been compared to models by solving the underl

14 Foulant characterization was performed by CLSM, AFM, ATR-FTIR, pyrolysis GC-MS, and ICP-MS techniq

15 The new insights provided by CLSM imaging demonstrate that flow in the MJE, and impin

16 Mucosal biofilms were visualized by CLSM on 46 (92%) of 50 MEM specimens from children with

17 cence confocal laser scanning microscopy (EC-CLSM).

18 Performing EC-CLSM at electrode surfaces allows to monitor spatially r

19 This study shows that combining fluorescence CLSM with electrochemistry is a powerful tool to study e

20 For CLSM visualization, the jetted solution contains a fluor

21 les using a conversion constant derived from CLSM imaging of eggs injected with a measured quantity o

22 mulsion and process stability as observed in CLSM images, droplet size data and in the amount of hept

23 posed 3D reconstruction method on time-lapse CLSM image stacks of the Arabidopsis Shoot Apical Merist

24 ted in a confocal laser scanning microscope (CLSM), thus allowing not only simple lifetime measuremen

25 ole in a confocal laser scanning microscope (CLSM).

26 Confocal laser scanning microscopic (CLSM) images were obtained from MEM biopsy specimens and

27 f individual cells from Confocal Microscopy (CLSM) image slices.

28 l and multiphoton laser scanning microscopy (CLSM and MPLSM) showed that these fluorescent fatty acid

29 Confocal laser scanning microscopy (CLSM) and image analyses revealed a significant increase

30 mined by confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM).

31 FI using confocal laser scanning microscopy (CLSM) as well as a 2-aminoethyl-monoamide-DOTA group for

32 rescence confocal laser scanning microscopy (CLSM) for flow visualization is described, with a focus

33 e use of confocal laser scanning microscopy (CLSM) for noninvasive characterization of the internal p

34 orescent confocal laser scanning microscopy (CLSM) images (z-stacks) of stained cells and three types

35 nd nNOs, confocal laser scanning microscopy (CLSM) images of SS and nNOS labeling were compared to su

36 lticolor confocal laser-scanning microscopy (CLSM) images.

37 30 min, confocal laser-scanning microscopy (CLSM) revealed numerous patches of Con A and SYTO 9 stai

38 Confocal laser scanning microscopy (CLSM) showed higher occurrence of large fat globules aft

39 1 cells; confocal laser scanning microscopy (CLSM) showed localization at the plasma membrane, consis

40 Confocal laser scanning microscopy (CLSM) showed that the number of fungal cells attached to

41 ies with confocal laser scanning microscopy (CLSM) showed very different localization patterns for th

42 AXS) and confocal laser scanning microscopy (CLSM) studies suggested that the siRNA-loaded LPNs are c

43 Confocal laser scanning microscopy (CLSM) study reveals that cytomembrane disintegration all

44 rescence confocal laser scanning microscopy (CLSM) to quantify three-dimensional pH gradients near el

45 ected by confocal laser scanning microscopy (CLSM) with excitation 442 nm, or two-photon laser scanni

46 ocal laser fluorescence scanning microscopy (CLSM), and dynamic light scattering (DLS).

47 ication, confocal laser scanning microscopy (CLSM), and electrokinetic analysis.

48 udied by confocal laser scanning microscopy (CLSM), scanning electron microscopy (SEM), micro-Raman s

49 ning and confocal laser scanning microscopy (CLSM), than the nondisinfected groundwater biofilms.

50 ed using confocal laser scanning microscopy (CLSM).

51 ell from Confocal Laser Scanning Microscopy (CLSM).

52 logy and confocal laser-scanning microscopy (CLSM).

53 ns under confocal laser scanning microscopy (CLSM).

54 ed using confocal laser scanning microscopy (CLSM).

55 ethod of confocal laser scanning microscopy (CLSM).

56 means of confocal laser scanning microscopy (CLSM).

57 ed using confocal laser scanning microscopy (CLSM).

58 ed using confocal laser scanning microscopy (CLSM).

59 The method can be realized in a standard CLSM without any modifications.

60 The CLSM micrographs provided evidence of the substantial di

61 The CLSM porosity results are further compared to those obta

62 6 nm which was 2 to 8 times smaller than the CLSM resolution.

63 sed on physically orthogonal measurements to CLSM.

64 ment of GSH levels in individual cells using CLSM and TPLSM gave values of 3.0 +/- 0.5 and 3.5 +/- 0.

65 e current methods of 3D reconstruction using CLSM imaging require large number of image slices per ce

66 e obtained from whole calculus samples using CLSM.

67 luorescence spectroscopy in combination with CLSM revealed the silica-coated Au@MnO@SiO2 Janus partic