The Abner IR80 Series Inverted Biological/Fluorescence Microscope is a high-performance inverted microscopic imaging platform developed by Ibona Micro-Nano Technology specifically for cell biology, live cell imaging, tissue observation and multi-channel fluorescence experiments. Adopting infinity-corrected optical design and a highly rigid integrated body structure, the system integrates brightfield and multi-channel fluorescence imaging functions, and supports research-level tasks including cell culture observation, fluorescence labeling imaging and image analysis. Featuring high stability, convenient operation and strong expandability, the IR80 Series can meet diverse demands for inverted microscopic imaging from universities, research institutes, biological laboratories and medical research platforms.
I. Core Advantages
Inverted Structure Adapted to Cell Experimental Workflow
The objective lens is positioned below the sample, compatible with sample types including petri dishes, culture flasks and multi-well plates, facilitating cell culture observation and long-term imaging.
Infinity-Corrected Optical System
Delivers high resolution and low chromatic aberration with a flat field of view and excellent clarity, suitable for brightfield and fluorescence imaging.
Multi-Channel Epifluorescence Imaging
Supports a wide range of fluorescent dyes and labeling protocols. Different channel combinations can be flexibly configured to achieve high-contrast fluorescence observation.
Modular Design and Upgradable Configuration
Filter sets, fluorescence light sources, digital cameras and software functions can be configured according to experimental requirements.
High-Stability Body and Precision Mechanical Structure
An integrated metal frame paired with a precision stage ensures high repeat positioning accuracy and stable long-term imaging.
## II. Technical Specifications (Typical Configuration)
### Optical System
Optical Type: Infinity-corrected optical system; Microscope Configuration: Inverted; Observation Modes: Brightfield / Fluorescence / Digital Imaging (Optional)
Eyepiece System: Eyepiece Type: Wide-field high-eye-point eyepiece; Standard Magnification: WF10×; Field Number: ≥ 22 mm
Objective System: Objective Type: Plan Achromatic Objective (Long Working Distance)
Standard Magnification Configuration: 4× / 0.10; 10× / 0.25; 20× / 0.40; 40× / 0.60 (Long Working Distance); 60× / 0.70 (Optional); Objective Mount: Standard RMS Thread
Objective Revolver
Type: Inclined objective revolver; Number of Positions: 4-position / 5-position (Optional); Equipped with positioning mechanism
Stage
Type: Fixed stage (Compatible with manual or motorized XY stage); Stage Compatibility: Suitable for petri dishes, cell culture flasks and multi-well plates; Student Stage Accessories (Optional): Multi-well plate holder, petri dish tray
Focusing System
Type: Coaxial coarse/fine focusing; Fine Focus Resolution: ≤ 1 μm; Anti-collision limit device
Brightfield Illumination System
Illumination Mode: Transmitted brightfield; Light Source: High-brightness LED cold light source; Brightness Adjustment: Continuously adjustable
Fluorescence System
Excitation Mode: Epifluorescence; Light Source Type: High-power LED fluorescence light source / High-pressure mercury lamp (Optional); Common Filter Sets (Optional): DAPI, FITC, TRITC, Cy5
Channel Quantity: 2–4 channels (Expandable); Fluorescence Filter Switching Mode: Manual / Motorized (Optional)
Digital Imaging System (Optional)
Camera Interface: C-mount / USB3.0 / HDMI
Supported Camera Types: Research-grade microscope camera / Educational camera
Software Functions:
Real-time display, image capture / snapshot / video recording, dimension measurement / annotation, multi-channel image overlay
### Electrical and Environmental Conditions
Power Supply: AC 100–240 V, 50/60 Hz; Operating Temperature: 5–40 ℃; Relative Humidity: ≤ 80% (Non-condensing)
III. Typical Application Fields
Observation and recording of cell culture processes; fluorescent labeling imaging of live cells; research on cell behaviors and dynamic processes; fluorescent observation of pathological tissues; analysis of drug effects and cellular responses; integration of experimental workflows for multi-well plates/culture dishes
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