This technology is widely adopted in scientific and industrial, for life science, material, or semiconductor  inspection. However, the cost of the mature commercialized system is usually very high.

SIMTRUM see the needs of the customer to have a robust confocal microscope system with reasonable cost. Our SIMSCOP Series offers a great balance between functionality, cost, and flexibility. 

Key Advantage

● Professional software UI with great features for imaging analysis 

● Single or Multi laser Channel, laser power control accuracy up to 0.01%,

● Silicon PMT detector enabling higher photon dynamic range and less noise.

● Support high-speed scanning: 30fps@512x512 Pixels(Resonant scanner)

● Compact Modular design, able to adapt to most microscope system 

● Multiple upgrade options for future capability expansion with low cost 

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Standard Wavelength：

405nm/488nm/561nm/640nm(638nm)

Optional Wavelength

UV：375 nm

VIS：445nm/473nm/515nm/525nm/532nm

         /633nm/660nm/685nm

NIR：785nm/808nm

6 Channel Laser module is optional

Silicon PMT Detector Enabling Higher QE and Less Noise

SIMSCOP CM Series confocal microscope equipment with SiPM Detector 

● Low-voltage operation

● Long operating life,

● Wider dynamic range

● Insensitivity to the magnetic field 

● Suitable for High-speed and High-SNR imaging

Upgrade to Confocal Spectral Microscope (Near IR I/II Confocal)

● Upgrade to Confocal Spectral Microscope (NIR I/II confocal)

● Wavelength Range UV to NIR (200nm-2.5nm)

● Spectral resolution up to 0.2nm

● Large NA setup for high-sensitivity application

Details Click here

Upgrade to High Speed Lines Scan Confocal Microscope

● Frame Rate 210fps 

● Resolution: 150 nm over the optical diffraction limit

● Imaging Depth of 500 to 1000 microns 

● Image Contract enhancement 20-30 dB

Details Click here

Upgrade to Terahertz Confocal Microscope 

System

● 100GHz, output power: 80mW

● Spatial resolution 150-200um

Drosophila brain; triple antibody staining:

Alexa 488, Alexa 568 and Alexa 633

Confocal micrograph of Arabidopsis thaliana (thale cress)

Seeding leaf with stomata(yellow moth-like structures)

And parenchyma cells.

Glioblastoma cells in culture transfected with a green fluorescent protein. The nuclei are stained blue with DAPI. The red spots are 0.02-micron fluorescent spheres that have been taken up into the cells by endocytosis. These cells have no endogenous P10 protein; P10 is a tumor suppressor gene that is mutated in many different types of cancer. The absence of the P10 protein is thought to increase cell mobility and possibly contribute to metastasis.

Shown is a confocal microscope image of a human gingival fibroblast in culture. Interphase microtubules (green) are labeled with alpha/beta-tubulin primary antibodies. FITC conjugated secondary antibody was applied afterward. Nuclear DNA (blue) was stained with Hoechst33242.

Live mitotic HeLa cell treated with epsin1 siRNA, DiOC6(3)to label mitotic membranes (green). Confocal images were taken at 0.118 μm steps along the Z-axis.

Pollen grain-3D

Time Correlated Single Photon Counting (Solution) For SPAD APD Testing 

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