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. | Italia

Skip to main content

Confocal Microscope

Richiesta di preventivo

A confocal microscope that captures images with a 25 mm field of view, nearly twice the area of conventional point scanners.

A1-HD25

A1 HD25 configured with inverted microscope Ti2-E

Capturing images of large samples such as tissues, organs and live model organisms requires both extending the detectable area of cellular responses and increasing image capture speed. The A1 HD25/A1R HD25 confocal microscope has the largest field of view (25 mm) in its field, enabling users to expand the limits of scientific research.

A1 HD25 Special Site

Caratteristiche salienti

See more than before in confocal resolution

a1rhd25-see-more

New 25mm FOV

When combined with the Ti2-E inverted microscope, the imaging area of the A1 HD25/A1R HD25 is nearly twice the conventional FOV of 18 mm, enabling the user to obtain significantly more data by capturing more of the specimen in each shot.


Fewer total images required for large high-resolution image stitching

The large 25 mm FOV of the A1 HD25/A1R HD25 reduces both the required number of images for stitching large images and image acquisition times, enabling efficient, high-throughput imaging of even large-scale samples. The number of required images can be greatly reduced, in particular for large 3D (XYZ) image stitching.

pic_04

FOV 25 of A1 HD25/A1R HD25: a total of 24 frames

pic_05

Conventional FOV 18: a total of 48 frames


Increase analytical throughput without compromising image resolution

The combination of a high-speed resonant scanner and large field of view forms an ideal platform for high-resolution screening assays. It dramatically reduces the time needed to analyze multiple samples and conditions.

pic_06

A well in the 96-well plate is selected

pic_07

The large FOV enables acquisition of entire wells (with a 4X objective)

pic_56

Large FOV enables measurement of larger areas and high-throughput analysis.


A1R HD25 high-speed, high-definition resonant scanner

High definition imaging up to 1K x 1K

1024 x 1024 pixels enables acquisition of high-resolution, high-quality images at lower magnifications, enabling compatibility with a wide range of samples.

1K-Resonant-zoom-8x-ave16---Deconvolved,-TypeAutomatic2
1K-Resonant-zoom-6x-ave16-zstack_3---Deconvolved,-TypeAutomatic5stacks2

Comparison of a large FOV image and 6X zoomed image (1024 x 1024 pixels) of fine structures in a 2 mm brain slice of H-line mouse cleared with RapiClear1.52, SunJinLab.
Image courtesy of: Drs. Ryosuke Kawakami, Kohei Otomo, and Tomomi Nemoto, Research Institute for Electronic Science, Hokkaido University

Low phototoxicity for live cells

High speed imaging capability up to 720 fps, in combination with a large field of view, dramatically increases imaging throughput. This scanning method reduces the exposure time of the sample to excitation light, minimizing phototoxicity and photobleaching.

Galvano scanner

pic_09
pic_10
pic_57

Resonant scanner

pic_58
pic_59
pic_60

Comparison of photobleaching of fluorescent proteins when images are acquired using both galvano and resonant scanners. 3D time-lapse images of trunk vasculature in zebrafish larva expressing LIFEACT-mCherry (probe for F-actin) in endothelial cells were acquired every 30 minutes over a period of 15 hours using a galvano scanner (average of 2 images) and a resonant scanner (average of 64 images).
1024 x 512 pixels, 2X zoom, 100 Z-stack images
Note that photobleaching of LIFEACT-mCherry was dramatically suppressed using the resonant scanner.
Image courtesy of: Shinya Yuge Ph.D., and Shigetomo Fukuhara, Ph.D., Department of Molecular Pathophysiology, Institute of Advanced Medical Sciences, Nippon Medical School

3D imaging of live cells

Secretion of Paneth cell granule in response to carbachol was acquired by high-speed 4D live imaging (acquisition of 61 steps of Z-stack images at 1.98 s/volume using Piezo Z-stage and 1K resonant scanner) using enteroids, the three dimensional culture of intestinal epithelial cells. As the innate immune response, the secretion of Paneth cell granules (green) one by one into enteroid lumen is clearly observed with high-definition 3D time-lapse imaging.

Green: Zinpyr-1 (Paneth cell granules), Purple: CellMaskTM Deep Red (plasma membrane)

Excitation wavelength: 488 nm, 638 nm Resolution: 1024 × 512 pixels

Image courtesy of: Dr. Yuki Yokoi, Dr. Kiminori Nakamura, Dr. Tokiyoshi Ayabe, Innate immunity Laboratory, Department of Cell Biological Science, Faculty of Advanced Life Science, Graduate School of Life Science, Hokkaido University

Time-lapse imaging of angiogenesis in zebrafish embryos expressing LIFEACT-mCherry (probe for F-actin) and MYR-GFP (probe for plasma membrane) in endothelial cells. 3D time-lapse images were acquired every 2.5 minutes for 14 hours starting from 22 hours post-fertilization using a resonant scanner (average of 64 images).

1024 x 1024 pixels, 2X zoom, 68 Z-stack images

Note that rapid formation and retraction of endothelial filopodia during angiogenesis has been clearly captured.

Image courtesy of: Shinya Yuge Ph.D., and Shigetomo Fukuhara, Ph.D., Department of Molecular Pathophysiology, Institute of Advanced Medical Sciences, Nippon Medical School


Superior images for both macro and micro imaging

Capture large-scale overview images as well as high magnification images with the same instrument. The 25mm FOV of the A1 HD25/A1R HD25 is effective for observation of large samples, while its 1Kx1K high-definition is ideal for the observation of minute structures.

A1RHD25-macro-micro

Stitched overview image of marmoset brain captured with CFI Plan Apochromat Lambda 10X objective and detailed image of dendritic spines captured with CFI SR HP Plan Apochromat Lambda S 100XC Sil objective


Highly sensitive detector options for various types of fluorescence labels

A1-DUG-2 GaAsP Multi Detector Unit

The A1-DUG-2 is a 4-channel detector unit equipped with high-sensitivity GaAsP PMTs, allowing acquisition of bright signals with minimal background noise, even when fluorescence is weak or the detector unit is used with a high-speed resonant scanner.

Images of HeLa cells labeled with MitoTracker, together with their intensity surface plots. Fluorescence intensities are indicated together with colors and heights in the 3D graph. There are major differences between GaAsP PMT (left) and Multi-Alkali PMT (right) in the background noise of and temporal change in the image.

A1-DUVB-2 GaAsP Detector Unit

A1-DUVB-2 is equipped with a high-sensitivity GaAsP PMT and allows spectral imaging using both galvano and resonant scanners. This is a fully tunable emission detector unit capable of spectral imaging with user-defined emission bandwidths as low as 10 nm. Variable bandpass mode and continuous bandpass mode are selectable based on the applications and the images can be spectrally unmixed. The option to add a second fixed bandwidth emission channel enables simultaneous multi-channel imaging.

pic_11

VB (Variable Bandpass) mode

pic_12

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

pic_13

Unmixed Image CB (Continuous Bandpass) mode

pic_14

CB (Continuous Bandpass) mode allows maximum 32 chspectrum imaging

HeLa cells labeled with five-color fluorescence, Nucleus: DAPI, Vimentin: Alexa Fluor® 488, Lamin: Alexa Fluor® 568, Tubulin: Alexa Fluor® 594, Actin: Alexa Fluor® 633
Specimen courtesy of: Dr. Tadashi Karashima, Department of Dermatology, Kurume University School of Medicine

A1-DUS Spectral Detector Unit

The A1-DUS can acquire spectral images at a high wavelength resolution of at least 2.5 nm. 32 channels of fluorescence spectra (up to a 320 nm wavelength range) can be acquired with a single scan, enabling fast imaging at up to 24 fps (512 x 32 pixels). Simultaneous excitation with up to four lasers enables spectral imaging across wider bands.

It precisely unmixes closely overlapping spectra of fluorescent labels and eliminates autofluorescence. Real-time unmixing during image acquisition is highly effective for FRET analysis.

pic_15

Spectral and unmixed images of five-color-fluorescence-labeled HeLa cells
Specimen courtesy of: Dr. Tadashi Karashima, Department of Dermatology, Kurume University School of Medicine

The unique V-filtering function, with its capacity for filter-less intensity adjustment, allows arbitrary spectral ranges to be selected from 32 channels and combined to perform the filtering function of up to four filters, enabling imaging with the optimal intensity of each fluorescence probe.

pic_22

Superior optical technologies to support all confocal applications

pic_23

Nikon provides a broad range of high-NA objectives with unrivaled optical quality to redefine the boundaries of confocal imaging. Options include silicone oil immersion objectives for thick live cell imaging, large-FOV low-magnification objectives and easy-to-use dry objectives. Chromatic aberrations are corrected from ultraviolet to near infrared range, enabling excellent multicolor imaging.

Detailed image of deep hippocampus cleared with RapiClear/SunJin Lab and captured with CFI Apochromat LWD Lambda S 20XC WI
Neural circuit (green) and blood vessel (magenta) of spinal cord cleared with RapiClear/SunJin Lab captured with CFI Apochromat LWD Lambda S 20XC WI

Options for high-speed live cell imaging during photostimulation

A1HD25-light-path

Simultaneous A1 HD25/A1R HD25 imaging and photostimulation

A new photostimulation module, featuring point scanning for stimulation of user-defined regions of interest, is available for the Ti2-LAPP modular illumination system and enables the A1 HD25/A1R HD25 to acquire confocal images while simultaneously stimulating the desired area of a sample. A DMD module simultaneously stimulates multiple regions of interest of any user-defined shape.


A unified acquisition and analysis software platform

NIS-Elements C, Nikon's unified software platform, provides an intuitive workflow for confocal imaging. With graphical programming tools for automating acquisition and analysis, the comprehensive operational environment can be fully customized for any level of application needs.

Enhanced Resolution

Higher resolution images can be generated with a single click. The software assesses the captured image and automatically determines processing parameters to achieve increased resolution. The unique image processing technology increases image resolution beyond that of a conventional confocal image (resolution can be improved 1.5 times (XY), 1.7 times (Z)).

Image courtesy of: Drs. Yutaro Kashiwagi and Shigeo Okabe, Department of Cellular Neurobiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo.

NIS-Elements HC (High-Content Analysis)

With fully-automated acquisition and analysis of a large number of high-content, multidimensional images following an easy stepwise workflow, HCA offers quick experimental setups and an immediate view of measurement data, well by well, during acquisition, and via a heat map for trend observation and further analysis.

pic_27

JOBS

Enables the easy creation of more complex and customized experimental templates, from image acquisition to analysis, without the need for advanced data programming knowledge. JOBS automatically conducts observation processes such as image acquisition, image and data analysis and result display. It improves efficiency and reduces the time needed for acquisition, analysis and mining of data.

pic_28

Setting of image stitching

pic_29

General Analysis

This is a toolbox of powerful segmentation functions that allows users to create custom analysis routines focused on obtaining statistical data from microscope images. Users can make easy to follow interfaces for image analysis, and interactively (or fully automatically) analyze images and output custom results.

pic_30

Setting of neuron measurement

pic_31
pic_65

Result of measurement



Back to top