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Stained sections were analysed using TissueMap (Definiens, Munich, Germany).
Immunostained sections were analysed using a Leica Leitz DMRD bright field microscope and a Zeiss confocal microscope (LSM 510, Carl Zeiss, Jena).
The sections were analysed using a Nikon inverted microscope (Nikon Eclipse TE-2000-S TE-2000-S TE-2000-S) equipped with a 150 W Xenon lamp and a 100X, 1.3 numerical aperture, epifluorescence oil immersion oBirlingam
All sections were analysed using a Leica DMLB fluorescence microscope and charge couple device (CCD) camera.
The stained sections were analysed using the Aperio imaging system (Aperio Technologies, California).
Stained cross sections were analysed using different filter cubes and 20× and 40× objectives.
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Each of six serial cross sections was analysed using a software-coupled (Image Pro Plus for Windows, v3) Nikon Eclipse E400 microscope and data were averaged.
22 Human sections and monolayer cells were analysed using (anti-CXCR1, -CXCR2 or CXCL6 (R&D)) primary antibodies followed by Cy2 conjugated goat anti-mouse IgG secondary antibodies (Jackson ImmunoResearch).
DNA structures were analysed using 3DNA26.
Group differences were analysed using repeated measures ANOVAs.
Results from the four SST variants were analysed using response times (RTs) and accuracy measures.
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