

LED Fluorescence Microscope
LED 荧光显微镜
- SKU FLM-0003
- Fluorescence Microscopes
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Optical system | Infinite corrected, fluorescence |
|---|---|
| Excitation wavelengths | 365, 470, 530, 625 nm |
| Light source | High-power LED modules |
| Filter cubes | DAPI, FITC, TRITC |
| Objectives | 10×, 20×, 40×, 100× |
| Eyepiece | 10× widefield |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 8036, ISO 19012-1, ISO 9345-1
What is the LED Fluorescence Microscope?
An LED fluorescence microscope uses light-emitting diodes instead of arc lamps for excitation. It offers stable, instant illumination with low heat and long life, making fluorescence imaging easier to use in routine and field laboratories.
What is the LED Fluorescence Microscope?
An LED fluorescence microscope uses light-emitting diodes instead of arc lamps for excitation. It offers stable, instant illumination with low heat and long life, making fluorescence imaging easier to use in routine and field laboratories.
Overview
An LED fluorescence microscope replaces the mercury or xenon arc lamp with one or more high-power light-emitting diodes, usually at wavelengths matched to common fluorophores such as 365, 470 and 530 nm. Diodes reach full intensity immediately, need no warm-up and have long service life, so the illumination is consistent between sessions. The narrow emission reduces the need for excitation filtering and lowers heat and ultraviolet exposure of the specimen. Intensity is electronically controlled, which supports quantitative imaging and reduces photobleaching. Filter cubes or interchangeable LED modules select the channel. The design is compact and stable, and it is increasingly used where arc lamp hazards and running costs are undesirable.
How does it work?
A fluorescence microscope illuminates the specimen with a selected excitation wavelength using a filter cube containing an excitation filter, a dichroic mirror and an emission filter. Fluorophores in the specimen absorb the excitation light and emit at longer wavelengths. The dichroic mirror reflects the excitation light onto the specimen and transmits the emitted light to the objective and detector, so background illumination is largely excluded. The specimen therefore appears bright against a dark background, giving high contrast and specificity. Multiple filter sets allow different fluorophores to be imaged in turn, and excitation and emission bands must be chosen to avoid overlap between channels. Bright sources, efficient filters and high-numerical-aperture objectives determine sensitivity.
What are the key features?
- LED excitation at wavelengths matched to fluorophores
- Instant full intensity without warm-up
- Long diode life and low heat output
- Electronically controlled intensity for quantitative work
- Compact stable design with interchangeable modules
What are the technical specifications?
A typical led fluorescence microscope configuration offers optical system of Infinite corrected, fluorescence, excitation wavelengths of 365, 470, 530, 625 nm, light source of High-power LED modules, filter cubes of DAPI, FITC, TRITC, objectives of 10×, 20×, 40×, 100× and eyepiece of 10× widefield. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The LED Fluorescence Microscope is used in routine clinical fluorescence testing, field and point-of-care fluorescence microscopy, microbiology auramine and acridine orange staining and teaching and demonstration laboratories. Across the wider Fluorescence Microscopes class, laboratories also deploy it for immunofluorescence and cell biology, fluorescence in-situ hybridisation and microbiology and viability staining.
Which standards and certifications apply?
Relevant standards and methods include ISO 8036, ISO 19012-1, ISO 9345-1, ISO 8255-1 and IEC 61010-1. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Protect the specimen from unnecessary light to reduce photobleaching, and use the lowest excitation intensity that gives adequate signal. Select filter sets that match the fluorophores and avoid spectral overlap between channels. Keep filters, dichroic mirrors and objectives clean, since contamination causes background fluorescence and scattering. Mercury and xenon lamps need warm-up, consistent alignment and careful disposal, while light-emitting diodes are stable and long-lived. Verify background and uniformity with a blank slide before imaging. Record excitation and emission settings with the images for reproducibility, and maintain the camera and software for quantitative work.
How do I select the right LED Fluorescence Microscope?
Choose an LED fluorescence microscope for routine fluorescence work where stability, low heat and long life are valued. Confirm the diode wavelengths match the fluorophores and available filter cubes. LED sources are excellent for common channels such as DAPI, FITC and TRITC; for very demanding spectral work or laser-based confocal imaging, a different system is required.
How does it compare with other Fluorescence Microscopes variants?
Choose a fluorescence microscope when specific molecules must be detected through fluorescent labels or natural autofluorescence. Match the filter sets to the fluorophores in use, such as DAPI for nuclei or FITC for green emission, and confirm the excitation source covers all required wavelengths. Decide between an upright configuration for slides and sections and an inverted one for live cells in dishes. For optical sectioning and three-dimensional imaging, a confocal system is required. Consider LED sources for stability and low running cost versus arc lamps for very high intensity. Check objective numerical aperture, transmission and correction, and the camera sensitivity for the emission wavelengths used.
Full specifications
| Optical system | Infinite corrected, fluorescence |
|---|---|
| Excitation wavelengths | 365, 470, 530, 625 nm |
| Light source | High-power LED modules |
| Filter cubes | DAPI, FITC, TRITC |
| Objectives | 10×, 20×, 40×, 100× |
| Eyepiece | 10× widefield |
| Stage | Mechanical, 140 × 140 mm |
| Intensity control | Electronic, step or continuous |
| LED lifetime | Over 20,000 h |
| Power supply | 100–240 V AC or 12 V DC |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Routine clinical fluorescence testing
- Field and point-of-care fluorescence microscopy
- Microbiology auramine and acridine orange staining
- Teaching and demonstration laboratories
Key features
- LED excitation at wavelengths matched to fluorophores
- Instant full intensity without warm-up
- Long diode life and low heat output
- Electronically controlled intensity for quantitative work
- Compact stable design with interchangeable modules
Frequently asked questions about LED Fluorescence Microscope
For narrow wavelength bands matched to a fluorophore, a high-power light-emitting diode can deliver comparable or higher useful intensity than an arc lamp, because arc lamp energy is spread across the spectrum. For excitation at unusual wavelengths or for very weak signals, a laser may still be preferable.
No. Light-emitting diodes reach full output immediately and remain stable, so measurements can start at once and are consistent between sessions. This removes the warm-up and ageing corrections that arc lamps require and simplifies quantitative fluorescence measurement.
Yes, many LED fluorescence microscopes use interchangeable modules, so a channel can be changed by fitting a module of a different wavelength together with the matching filter cube. This makes wavelength flexibility less costly than changing an arc lamp and filter set.
A filter cube is a module holding an excitation filter, a dichroic mirror and an emission filter. The excitation filter selects the illumination band, the dichroic mirror reflects it to the specimen and transmits emitted light, and the emission filter blocks residual excitation light before the detector.
Fluorophores can be permanently altered by excitation light, a process called photobleaching. The rate depends on the fluorophore, the excitation intensity and the presence of oxygen. Using lower intensity, shorter exposure, antifade media and efficient filters slows bleaching and preserves the signal.
Standard epifluorescence microscopes image the whole depth of the specimen, so out-of-focus light reduces contrast in thick samples. Optical sectioning requires confocal or light-sheet illumination, which restricts detection to a thin focal plane and enables three-dimensional reconstruction.
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