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The images recorded with the microscope were analyzed by standard image processing methods, and the average sizes of agglomerates and their uncertainties were determined.
Images obtained on the confocal microscope were analyzed using Fiji software (Schindelin et al., 2012).
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The performance of the novel light field microscope is analyzed theoretically and experimentally.
Expression of c-Fos and BDNF protein observed under the fluorescent microscope was analyzed by using software ImageJ (NIH, USA).
Cover slips were mounted with a mix of polyvinyl alcohol and glycerol, and the microscope slides were analyzed on a Zeiss confocal microscope with a 63× magnification.
Cover slips were mounted with a mix of polyvinyl alcohol and glycerol, and the microscope slides were analyzed on a Leica LEITZ DM microscope with a 100× magnification.
Images were obtained using a Nikon Ti-E microscope and were analyzed by NIS software modules (Nikon Instruments Inc., Melville, NY, USA).
Images were captured using a Zeiss LSM780 confocal microscope, and were analyzed in ZEN 2011 software.
Images were recorded using a Gatan DualVision 600t CCD camera attached to the microscope and were analyzed using Gatan Digital Micrograph Version 3.11.1.
The images were captured on FluoView FV1000 (Olympus, Tokyo, Japan) or LSM510 version 3.2 (Carl Zeiss, Jena, Germany) confocal laser-scanning microscope and were analyzed using the FV1000 and LSM510 software.
Aliquots of fractions having virus particles based on PAGE and electron microscope analyses were analyzed by SDS-PAGE.
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