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The Spectralis HRA+OCT has been used in imaging the choroid in intraocular inflammation using the inverted scan technique.
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All pictures were captured on an LSM 510 inverted scanning confocal microscope in the NICHD Microscopy and Imaging Core facility.
Table 1 FET-PET repeat scan results Number of patients Both scans non-inverted 13 Both scans inverted 2 One scan non-inverted, other inverted 2 A sample patient from the last row is shown in Figure 1. Figure 4 Effect on PET of simulated fat/water inversion.
Cells were examined by laser confocal microscopy (Zeiss LSM 410 Invert Scan Microscope) using single or double-labeling immunocytochemical fluorescence (FITC, Cy3) and colloidal gold to reaffirm the subcellular locations of taxol, the taxane ring (baccatin III), the C-13 side chain of taxol, and taxanes in general.
A Leica DM IRB with TNC-NT confocal scanning laser microscope (Leica TCS SP/DM IRB inverted confocal scanning microscope; Leica Microsystems GmbH, Wetzlar, Germany) was used for the confocal microscopy recordings.
The cover slips mounted on glass slides with 15 µl Mowiol mounting medium were immediately observed via a Leica AOBS TCS SP5 inverted laser scanning confocal microscope.
Confocal fluorescence images were collected using a Zeiss LSM700 inverted laser scanning microscope.
Leica AOBS TCS SP2 inverted laser scanning confocal microscope (LSCM) was used for cell imaging.
Observations were made using a Zeiss LSM 510 inverted confocal scanning microscope.
Samples were examined using Olympus FV1000 or Nikon A1 inverted laser scanning confocal microscope.
The images were captured using a Zeiss LSM 510 inverted laser-scanning confocal microscope.
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