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Confocal Microscope System

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Key Features

Simple operation of complex applications

NIS-Elements C imaging software enables integrated control of the confocal imaging system, microscope and peripheral devices with a simple and intuitive interface. Various reliable analysis functions are also available.

Software-1

Basic operation

Software-2

Optical setting


A1 ER: Enhance Your Confocal Resolution

Using powerful GPU-based processing and specialized deconvolution algorithms, the spatial resolution of your A1+ [or A1R+] confocal microscope can be dramatically enhanced with minimal processing time.  

High quality PSF models for Nikon’s high performance objective lenses take the guesswork out of deconvolution analysis.  Other features include automatic or manual mode for iteration selection, enhanced spherical aberration correction, and robust algorithms for noise estimation and removal. 

With ER your theoretical resolution is your practical resolution.

a1er-conventional

Conventional confocal image

a1er-a1er

ER processed confocal image

Image credit:  Apical surfaces of auditory epithelia of mouse cochleae were stained by Atto-565-phalloidin at postnatal day 2.

Photographed with the cooperation of: Dr. Hideru Togashi, Division of Molecular and Cellular Biology, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine.

A1ER-zebrafish-lens

Image credit: Zebrafish lens at 5 dpf. Nuclei (green) and actin filaments (red) are visualized with Cytox-green and Rhadamine-conjugated phalloidin, respectively. High magnification images indicate lens fiber cells, which become flat and multi-stacked each other.

Photographed with the cooperation of: Drs. Toshiaki Mochizuki and Ichiro Masai, Developmental Neurobiology Unit, Okinawa Institute of Science and Technology Graduate University



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