Cookies on the Nikon Instruments website
We use cookies to ensure we give you the best experience on our website. If you continue we'll assume
that you are happy to receive all cookies on the Nikon Instruments website.
Find out more about our cookie policy

Nikon

Nikon Instruments Europe B.V. | Europe & Africa

Skip to main content

Confocal Microscope System

Request a Quote

An essential microscopy laboratory instrument

overview1

Configured with Ni-E upright microscope

The C2+ confocal microscope is a basic model within the family of Nikon confocal products. The C2+ is designed as an essential microscopy tool for the laboratory, providing powerful and robust imaging capabilities. The high-efficiency scan heads and detectors, coupled with Nikon's unrivaled optics, provide superior confocal images. The high-speed galvano scanners, operating at rates of up to 100 fps*, enable even the fast-beating motion of cardiac muscles to be captured with precision. The system also provides simultaneous acquisition of three fluorescent channels plus DIC in a single scan. For research that requires spectral imaging capabilities, Nikon's C2si+ system provides dedicated spectral detector units in addition to the standard fluorescence detector units. The C2si+system allows high-precision and high-speed 32-channnel spectral imaging or high-sensitivity spectral imaging. Built on a reputation of incredible stability and operational simplicity, coupled with superior optical technologies, the C2+ confocal system is the essential laboratory tool.

*with 8x zoom or larger

Key Features

High-speed acquisition of high-definition images

Galvanometer-based high-speed scanning enables confocal imaging of fast, dynamic events in live cells, such as the beating motion of cardiac muscle cells. In traditional confocal systems, fast bi-directional scanning can lead to pixel shifts. 

However, the C2+ confocal system's pixel shift correction mechanism ensures acquisition of the highest quality images even with fast bi-directional scanning.

Rat primary cardiac muscle cells labeled with Fluo-8 AM and MitoTracker® Orange are stimulated with histamine. 
Scanning speed: 15 fps


Image Quality

Nikon's unprecedented optics and a time-proven, highly efficient optical design provide the brightest and sharpest images, at the longest working distances.

High-efficiency scan heads and detectors

high-efficiency1

With the convenient, small scan head size, the C2+ can be used with various types of Nikon microscope. The C2+ employs high precision mirrors and optically superior circular pinholes, and separates the detectors to isolate sources of heat and noise, enabling low-noise, high-contrast and high-quality confocal imaging. The newly developed scanner driving system and Nikon's unique image correction technique allow 8 fps (512 x 512 pixels) and 100 fps (512 x 32 pixels) high-speed imaging.

high-efficiency23
high-efficiency24
high-efficiency25
high-efficiency26

High-performance optics

CFI Apochromat Lambda S Series

high-efficiency2

CFI Apochromat LWD Lambda S 20XC WI, NA0.95 
CFI Apochromat Lambda S 40XC WI, NA1.25 
CFI Apochromat LWD Lambda S 40XC WI, NA1.15 
CFI Apochromat Lambda S 60X Oil, NA1.49

These high-numerical-aperture (NA) objectives provide chromatic aberration correction over a wavelength ranging from ultraviolet to infrared and are ideal for multicolor confocal imaging. In particular, the LWD Lambda S 40XC WI lens has an extremely wide chromatic aberration correction range from 405 nm to near-IR. The transmission property of these lenses is enhanced through the use of Nikon's exclusive Nano Crystal Coat technology.


CFI Apochromat TIRF Series

high-efficiency3

CFI Apochromat TIRF 60X Oil, NA1.49 (left) 
CFI Apochromat TIRF 100X Oil, NA1.49 (right)

These objectives boast an unprecedented NA of 1.49 (using a standard coverslip and immersion oil), the highest resolution among Nikon objectives. Correction collars enable optimization of point spread functions for varying imaging temperatures, ensuring highest quality confocal images whether you are imaging at room temperature or 37 degrees Celsius.

High-definition diascopic DIC images

The C2+ can acquire simultaneous three-channel fluorescence or simultaneous three-channel and diascopic DIC observation. High-quality DIC images and fluorescence images can be superimposed to aid in morphological analysis.

high-efficiency6

DIC image

high-efficiency7

Overlay of DIC and fluorescence images


Intuitive operation

The superior operability and diverse analysis capabilities of the NIS-Elements imaging software satisfy both beginners and experienced confocal users. In addition, NIS-Elements allows for intuitive operation not only of Nikon microscopes but also of third party peripheral devices for a broad range of experiments.

Multimode capability

Various imaging methods, such as confocal, widefield, TIRF, photoactivation, as well as processing, analysis and presentation of acquired images, are available in one software package. Users can easily learn how to control different imaging systems with a common interface and workflow.

software1

Easy-to-recognize display for setting lasers, detectors, etc.

software2

Scanning parameter settings

Unmixing

software3

Spectral analysis GUI

Numerous functions for analysis and unmixing of acquired spectrums are provided, while spectral profiles of general dyes and fluorescent proteins are preprogrammed.


Fast and accurate spectral imaging: C2-DUS Spectral Detector Unit

High-speed spectral imaging

Acquisition of a 32-channel spectral image (512 x 512 pixels) with a single scan in 0.6 second is possible. Moreover, 512 x 32-pixel images can be captured at 24 fps.

Accurate and high-speed unmixing

spectral-imaging-1

Accurate spectral unmixing provides maximum performance in the separation of closely overlapping fluorescence spectra and the elimination of autofluorescence. Superior algorithms and high-speed data processing enable real time unmixing during image acquisition.

spectral-imaging-2

Actin of HeLa cell expressing H2B-YFP was stained with Phalloidin-Alexa Fluor® 488. 
Spectral image in the 500-692 nm range captured with 488 nm laser excitation 
Left: Spectral image, Right: Unmixed image (green: Alexa Fluor® 488, red: YFP) 
Specimen courtesy of: Dr. Yoshihiro Yoneda and Dr. Takuya Saiwaki, Faculty of Medicine, Osaka University

Wide band spectral imaging

Simultaneous excitation with four lasers selected from a maximum of eight wavelengths is available, enabling spectral imaging across wider bands.

V-filtering function

Filter-less intensity adjustment is possible by selecting desired spectral ranges from 32 channels that match the spectrum of the fluorescence probe in use and combining them to perform the filtering function.

spectral-imaging-3

Bright spectral imaging: C2-DUVB GaAsP Detector Unit

High-sensitivity spectral image acquisition

With a GaAsP PMT, the C2-DUVB tunable emission detector delivers flexible detection of fluorescent signals with higher sensitivity.

Variable acquisition wavelength range

User-defined emission bands can collect images within a selected wavelength range, replacing the need for fixed bandwidth emission filters. 
Users can define the emission bandwidth range to as little as 10nm. Spectral images of multi-labeled specimens can be acquired by capturing a series of spectral images while changing detection wavelengths.

Based on the application, virtual bandpass mode and continuous bandpass modalities are selectable on the C2-DUVB.
spectral29

VB (Variable Bandpass) mode Captured in 3 ch

spectral30

VB (Variable Bandpass) mode allows maximum 5ch color image

spectral31

CB (Continuous Bandpass) allows maximum 32 ch spectrum imaging

Optional second channel detector

An optional second GaAsP PMT provides flexibility in detection. Users can divert selected wavelengths to the 2nd fixed bandwidth emission channel by inserting a dichroic mirror, while simultaneously utilizing the user-definable emission band on the first channel. 
The second detector allows FRET, ratio imaging and other applications requiring simultaneous multi-channel imaging.

Accurate spectral unmixing

Multi-channel images acquired with the C2-DUVB can be spectrally unmixed by using the spectra of reference samples, or the spectra within the acquired images.


Flexibility

The C2+ can be coupled with upright, inverted, physiological, and macro imaging microscopes and has options for combinations with various high-quality research experiment systems. All can be controlled with NIS-Elements software.

TIRF/Photoactivation-C2+ Multimode imaging system

spectral13

With its output fiber switching system, the LU-NV laser unit can support multiple laser applications, such as C2+, TIRF and photoactivation. This enables high resolution confocal imaging, imaging of single molecules with an extremely high S/N ratio, and imaging of the fluorescence characteristic changes of photoactivated and photo-convertible fluorescent protein, all on a single microscope platform.

AZ-C2+ Macro confocal microscope system

spectral14

The AZ-C2+ macro confocal system enables confocal image acquisition of large specimens (> 1cm) with high resolution. Stunning, large field-of-view images with exceptionally high signal-to-noise ratios of whole embryos and large tissue slices can be captured in a single acquisition at pixel resolutions of up to 2048x2048. 

Moreover, the AZ-C2+ macro confocal offers a combination of low and high magnification objective lenses, variable optical zoom and confocal scanning zoom function, enabling continuous imaging from macro to micro with a single microscope. 

The AZ-C2+ macro confocal enables in vivo confocal imaging of macro specimens which is not possible with traditional stereoscopic microscopes.

flexibility15

TT2 ES cells 
Anti-Nanog antibody (Cy3), anti-Oct3/4 antibody (Alexa Fluor® 488) and DAPI localized in cell nuclei 

Photo courtesy of: Dr.Hiroshi Kiyonari, Laboratory for Animal Resources and Genetic Engineering, RIKEN Center for Developmental Biology

flexibility16

Photo courtesy of: Professor Masatoshi Yamamoto, Kyoto Institute of Technology



Back to top