In addition, the system easily can be set to operate in a discrete, one-shot mode designed to facilitate applications that require maintaining multiple focus positions, such as experiments involving multi-well imaging. The system is optimized for use with total internal reflectance fluorescence (TIRF) and other advanced applications.
The ZDC2 Zero Drift system uses a Class 1 785-nm laser diode to locate either the water/glass interface (for oil- or water-immersion objectives) or the air/glass interface (for non-immersion lenses). Samples can be mounted on coverslips, multi-well tissue culture plates, glass-bottom culture dishes or other glass substrates. Working in tandem with MetaMorph for Olympus software, ZDC2 Zero Drift uses an intermediate lens to focus to the desired z-position (depth) in the sample, automatically maintaining focus for seconds, hours, days or weeks. Using its automated continuous mode, users can easily retain precise focus even after reagents are added.
The IX81-ZDC2 Zero Drift provides crisp, sharp, bright images under time-lapse conditions. It can be used with a broad range of objectives including two key high-transmission Olympus TIRF lenses – the APON 60x, 1.49 NA and the UAPON 100x 1.49 NA objectives. ZDC2 Zero Drift also is an excellent choice for keeping focus during multi-modal calcium experiments that employ both TIRF and Fura-2. In conjunction with the Olympus cell^TIRF illuminator, the system allows simultaneous, high-speed multi-angle TIRF imaging.
The ZDC2 Zero Drift system uses a Class 1 785-nm laser diode to locate either the water/glass interface (for oil- or water-immersion objectives) or the air/glass interface (for non-immersion lenses). Samples can be mounted on coverslips, multi-well tissue culture plates, glass-bottom culture dishes or other glass substrates. Working in tandem with MetaMorph for Olympus software, ZDC2 Zero Drift uses an intermediate lens to focus to the desired z-position (depth) in the sample, automatically maintaining focus for seconds, hours, days or weeks. Using its automated continuous mode, users can easily retain precise focus even after reagents are added.
The IX81-ZDC2 Zero Drift provides crisp, sharp, bright images under time-lapse conditions. It can be used with a broad range of objectives including two key high-transmission Olympus TIRF lenses – the APON 60x, 1.49 NA and the UAPON 100x 1.49 NA objectives. ZDC2 Zero Drift also is an excellent choice for keeping focus during multi-modal calcium experiments that employ both TIRF and Fura-2. In conjunction with the Olympus cell^TIRF illuminator, the system allows simultaneous, high-speed multi-angle TIRF imaging.
The autofocus system is integrated into the Olympus IX81 microscope stand, known for its rigidity, stability and reliability. The small footprint of the IX81 houses a very efficient light path, and ZDC2 Zero Drift does not require the use of a second control pad or other accessories that can clutter the lab bench.
The ZDC2 Zero Drift tales advantage of the specimen-coverslip relationship. While the distance between the objective and coverslip can be affected by temperature, gravity, immersion media viscosity and other factors, the distance between the coverslip and an attached cell is much more stable. ZDC2 Zero Drift locates the specimen-coverslip interface very reliably and is able to return to the defined focus position with great accuracy, even if the objective-to-coverslip distance changes. Further, the system uses an autofocus routine that is significantly faster than conventional software-based algorithms and is unaffected by changes in morphology, contrast or fluorescence intensity of the cell. The laser can be turned off during periods when image acquisition is not occurring. In addition to TIRF, the autofocus system works well with high-throughput screening and other high-accuracy time-lapse studies of living cells in stage incubation systems.
The ZDC2 Zero Drift tales advantage of the specimen-coverslip relationship. While the distance between the objective and coverslip can be affected by temperature, gravity, immersion media viscosity and other factors, the distance between the coverslip and an attached cell is much more stable. ZDC2 Zero Drift locates the specimen-coverslip interface very reliably and is able to return to the defined focus position with great accuracy, even if the objective-to-coverslip distance changes. Further, the system uses an autofocus routine that is significantly faster than conventional software-based algorithms and is unaffected by changes in morphology, contrast or fluorescence intensity of the cell. The laser can be turned off during periods when image acquisition is not occurring. In addition to TIRF, the autofocus system works well with high-throughput screening and other high-accuracy time-lapse studies of living cells in stage incubation systems.
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