ライフサイエンスコーパス: laser scanning microscope

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1 Tissue was examined with a confocal laser scanning microscope.

2 nyl compounds were detected using a confocal laser scanning microscope.

3 examined under light microscope and confocal laser scanning microscope.

4 -labeled neurons was mapped using a confocal laser-scanning microscope.

5 tion (MSM) levels and visualized by confocal laser scanning microscope before being characterized by

6 anding wave can be produced in a single-spot laser scanning microscope by placing a plane reflector c

7 tissue sections were examined on a confocal laser scanning microscope by using dual channel immunofl

8 ining fluorophores that can be imaged with a laser scanning microscope can be analyzed using RICS.

9 Here, we show that the multiphoton laser-scanning microscope can provide high three-dimensi

10 The technique is implemented in a confocal laser scanning microscope (CLSM), thus allowing not only

11 ere stained and examined whole in a confocal laser scanning microscope (CLSM).

12 y after photobleaching (FRAP) using confocal laser scanning microscopes (confocal FRAP) has become a

13 Images obtained with a laser-scanning microscope contain a time structure that

14 Membrane repair assays with a two-photon laser-scanning microscope demonstrated that wild-type mu

15 Multi-photon laser scanning microscopes have many advantages over sin

16 Layer V neurons were imaged on a two-photon laser scanning microscope in fixed tissue sections.

17 Although the introduction of laser-scanning microscopes in principle could facilitate

18 rized including sequential registration with laser scanning microscopes, line imaging and global or w

19 A laser scanning microscope (LSM) with a supercontinuum la

20 ed with the software packaged with the Zeiss laser-scanning microscope (LSM AIM, version 3.2).

21 on of a plane mirror to an existing confocal laser scanning microscope, may well prove useful in stud

22 skin model with a near-infrared multiphoton laser-scanning microscope (NIR-MPLSM).

23 ld nanorods excited at 830 nm on a far-field laser-scanning microscope produced strong two-photon lum

24 Time-lapse analysis with a 2-photon laser scanning microscope revealed that the growth cones

25 Membrane repair assays using a two-photon laser-scanning microscope revealed that calpain 4-defici

26 giant unilamellar vesicles under a confocal laser scanning microscope show that a family of thermall

27 Optical sections taken with a confocal laser-scanning microscope showed that the Lewis antigen

28 nofluorescence localization under a confocal laser-scanning microscope, the BIS3 protein in the trans

29 imaging method can be applied to commercial laser scanning microscopes thereby making it accessible

30 ense illumination, such as at the focus of a laser-scanning microscope, these SHG nanocrystals conver

31 rom-thick plastic sections and with confocal laser scanning microscope, thus further supporting the f

32 ical modifications that need to be made to a laser-scanning microscope to enable the measurements.

33 s easily integrated into standard two-photon laser-scanning microscopes to generate an axially elonga

34 ges with an Olympus FluoView FV1000 confocal laser scanning microscope using Olympus FluoView softwar

35 approximately 8000 lines s-1), although the laser scanning microscope was limited to < 1000 lines s-

36 A confocal laser scanning microscope was used for detection.

37 By adapting a laser scanning microscope with a titanium sapphire femto

38 The Olympus IV100 Laser Scanning Microscope, with ultra-narrow microscope

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