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1 y a microleakage-testing device and confocal laser scanning microscope.
2 examined under light microscope and confocal laser scanning microscope.
3 -combined CPNE7 was confirmed under confocal laser scanning microscope.
4 Tissue was examined with a confocal laser scanning microscope.
5 nyl compounds were detected using a confocal laser scanning microscope.
6 -labeled neurons was mapped using a confocal laser-scanning microscope.
7 sses from single-color images collected with laser scanning microscopes.
8 tion (MSM) levels and visualized by confocal laser scanning microscope before being characterized by
9 anding wave can be produced in a single-spot laser scanning microscope by placing a plane reflector c
10 tissue sections were examined on a confocal laser scanning microscope by using dual channel immunofl
11 ining fluorophores that can be imaged with a laser scanning microscope can be analyzed using RICS.
13 The technique is implemented in a confocal laser scanning microscope (CLSM), thus allowing not only
14 ation microscopy data acquired on a confocal laser scanning microscope (CLSM), which will enable user
16 y after photobleaching (FRAP) using confocal laser scanning microscopes (confocal FRAP) has become a
18 Membrane repair assays with a two-photon laser-scanning microscope demonstrated that wild-type mu
21 scence measurements obtained with a confocal laser scanning microscope in biofilms: 1) linear drift,
24 rized including sequential registration with laser scanning microscopes, line imaging and global or w
27 on of a plane mirror to an existing confocal laser scanning microscope, may well prove useful in stud
30 ld nanorods excited at 830 nm on a far-field laser-scanning microscope produced strong two-photon lum
32 Membrane repair assays using a two-photon laser-scanning microscope revealed that calpain 4-defici
33 giant unilamellar vesicles under a confocal laser scanning microscope show that a family of thermall
35 nofluorescence localization under a confocal laser-scanning microscope, the BIS3 protein in the trans
36 imaging method can be applied to commercial laser scanning microscopes thereby making it accessible
37 ense illumination, such as at the focus of a laser-scanning microscope, these SHG nanocrystals conver
38 rom-thick plastic sections and with confocal laser scanning microscope, thus further supporting the f
39 ical modifications that need to be made to a laser-scanning microscope to enable the measurements.
40 s easily integrated into standard two-photon laser-scanning microscopes to generate an axially elonga
41 ges with an Olympus FluoView FV1000 confocal laser scanning microscope using Olympus FluoView softwar
42 approximately 8000 lines s-1), although the laser scanning microscope was limited to < 1000 lines s-
45 an be easily implemented on a Leica confocal laser scanning microscope, with better photon efficiency