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Is there another way to focus the second interface???
What exactly is there in front of the two detectors? Is there any light focusing mechanism there for improving the counts?
The beam after pinhole is collimated an then focussed on the detector. The reason is that the active area of the detector is typically small
This video is awesome and helpful. Thank you buddy....
how much does this cost?
Thank you for your interest in our confocal microscope MicroTime 200. The system is modular and is configured according to the customer's needs.Please contact us via info[at]picoquant.com if possible already with your requirements and application.
Is there another way to focus the second interface???
What exactly is there in front of the two detectors? Is there any light focusing mechanism there for improving the counts?
The beam after pinhole is collimated an then focussed on the detector. The reason is that the active area of the detector is typically small
This video is awesome and helpful. Thank you buddy....
how much does this cost?
Thank you for your interest in our confocal microscope MicroTime 200. The system is modular and is configured according to the customer's needs.
Please contact us via info[at]picoquant.com if possible already with your requirements and application.