Unique Self-contained Confocal Laser Scanning Unit

A Unique, Easy-to-use, Self-contained Confocal Laser Scanning Microscope with a Small Footprint

The FV10i features a unique self-contained design. Simplified and optimized, key components, including an incubator and laser combiner, have been integrated into a self-contained package with no compromises. The system, which is easier to set up and use, features the same functionality as a high-end confocal laser scanning microscope while adding vibration isolation and a light tight cover. As a result, the FV10i can be operated by new and experienced users alike and, with a compact footprint, can be installed in any laboratory without the need for a dedicated dark room.

High-definition Images using Advanced Optics

Equipped with 4 Diode Lasers

The system is equipped with four (405/473/559/635 nm) lasers. Multi-stained specimens can be imaged with up to four fluorescence dyes. Maintenance-free and power-saving diode lasers with longer operating lives are employed in all the laser units, and operate with low noise levels.

Detector Utilizes a Newly Developed Spectrum Method

The detecting mechanism has two fluorescence channels, and one phase contrast channel. The fluorescent channels use a newly developed spectrum method comprising grating, beam splitter, and slit. In addition, they are equipped with the variable barrier filter function where the most suitable wavelength width is set automatically in accordance with the characteristics of the fluorescence dye.

Two Sequential Modes

The FV10i is equipped with two sequential modes. Images can be acquired through line sequences without crosstalk in imaging with two fluorescence dyes, and with three or four dyes in frame sequences with the virtual channel function.

Objectives of 10× and 60× are System-mounted

The system is equipped with objectives of 10× and 60×. Zoom magnification can be changed continually from 10× to 600×. The most suitable imaging area can be set depending on the size of the specimen.

Start Capturing Images from the First Day

Stress-free Operation for Every User

Only two manual steps are required of the user: placing of the specimen on the stage and closing the cover. After that, the sophisticated user interface offers clear and efficient operation of the microscope. The selection of the imaging point, for example, can be performed easily using the newly designed image mapping menu without need for special experience or expertise. Furthermore, using advanced functionality that is only found in Olympus products, automatic focus and intensity adjustment allow the imaging conditions to be set up according to the type of specimen and observation mode required. In addition, the system is equipped with a navigation function that identifies the operational step of the imaging procedure and guides the operator to the next appropriate operation. The FV10i confocal laser scanning microscope, therefore, provides a stress-free and comfortable operating environment even for first-time users.

Setting

Place a specimen, and select a fluorescence dye. The FV10i automatically selects the most suitable imaging conditions based on the fluorescence dye selection.

Image Mapping Menu

Just click the <Start> button, and a map image of the specimen is created automatically. Users can then easily identify the desired image acquisition point.

Image Capturing

Through the sophisticated operating software, the image capture area or zoom magnification can be set quickly. Image capture is then completed at the click of a button.

Capture a Map Image Easily for Navigation

When the Specimen Has Been Loaded, Clicking <Start> Begins the Mapping Process

Following the loading of the specimen, a map image can be acquired by simply clicking the <Start> button in the "Acquire Map Image" window. With this bird's-eye view of the specimen, the user can quickly and easily select the imaging area to be captured.

Create Map Area

The map image provides the user with an overview of the possible image capture area. The selectable map areas are automatically displayed in a diagram according to the type of specimen holder that has been used, such as a 35mm diameter dish or glass slide. An area can be selected and map image acquired by clicking on the desired scan area in the diagram. This will display an overview image of the area on the “Map Image” screen. Selecting an alternative area requires just a single click operation.

Fluorescence Dye Selection

A separate map image can be displayed for each fluorescence dye. These images can be displayed individually or be overlaid with each other.

Scanning Setting

One of two scanning orders can be selected depending on the experimental requirements.

Automatic
A map image is automatically acquired from the center outward in a spiral pattern, allowing even a first-time user to easily identify the confocal view area.

Manual
The desired map image areas can be selected directly up to a maximum 9 × 9 area. Manual selection is more efficient than automatic selection as the ROI (Region of Interest) can be narrowed down in advance.

A Map Image of the Specimen Can be Automatically Created

A map image can be created by automatically detecting which type of specimen holder is used. High speed with low resolution or low speed with high resolution image mapping options is available.

Easy Guided Operation for First-time Users

Sophisticated Menus Allow Easy Navigation of Imaging Area

The desired imaging region can be selected using the map image and live image screens utilizing the zooming function of the intuitive user interface. The user friendly navigation functions allow even a first-time user to capture images with ease.

The System is Equipped with a User Friendly Navigation Function

Clicking the <Navigation> button shows the operational procedure and highlights the operational button. Just follow the navigational guidance to easily complete your imaging.

Stitching Function

Wide-angle high-resolution imaging can be obtained by acquiring the adjacent regions. A map image of the entire glass slide can also be created.

Dedicated Analysis Software Exclusive to FLUOVIEW

Dedicated Olympus software is provided as part of the standard specifications, bringing editing and analysis capabilities to images taken by FV10i.

File Input/Output

OIF (Olympus Image Format) is employed to store various parameter settings and images together. This software supports a wide range of well-used formats with high interchangeability including TIFF, BMP and JPEG.

High Efficiency Imaging with the Olympus FV10i-DOC

The system is equipped with an original UPLSAPO–equivalent Olympus objective, which is intended to provide the best fluorescence observation performance available in the world for a 60X objective. The objective has a high numerical aperture of 1.35 enabling high resolution imaging. The FV10i motorized stage automatically moves to the oil supply position when switching to the oil immersion objective, allowing oil to be supplied efficiently without removing the specimen.

Feature-rich Functionality for Stress-free Imaging

Equipped with Specimen Holders

The system is equipped with specimen holders, usable for a dia. 35 mm glass bottom dishes, glass slides, cover glass chambers (8 wells type), and well slides (8 wells type). Specimens can be observed without the risk of contamination using the closed contamination-free plastic cover of a dia. 35 mm glass bottom dish.

Capturing Adjacent Images in Wide field

Imaging of adjacent images is possible to create big mosaic images. These can be captured in high-definition and wide field of view.

HDD Recording for Storing Large Volumes of Data

The microscope comes equipped with a HDD (hard-disk drive) recording function. The images captured are stored automatically in the HDD. Large volumes of data, such as those obtained from long-term time-lapse imaging can be stored. During imaging, editing/analysis of previously taken images is also possible. An external HDD connected to a network can be specified as the destination, and the saved images can be viewed on a remote PC while performing separate imaging.