
Zeiss LSM 900 with Airyscan 2 & jDCV
Zeiss LSM 900
This inverted (Axio Observer 7) confocal imaging workstation produces super-resolution, high-contrast images while minimizing light exposure, to reduce photobleaching and channel bleed-through. The system has a diode laser module allowing for light emission at 405 nm, 488 nm, 561 nm, and 640 nm. It utilizes two GaAsP PMT detectors, one transmitted light detector, and an Airyscan 2 detector with Multiplex Mode for super-resolution imaging along with adaptive focusing capabilities. The Airyscan 2 is an area detector with 32 detection elements which allows for rapid confocal imaging for spatial and temporal recordings, as well as generating mosaic tiling for multidimensional reconstruction. The microscope performs deconvolution using LSM Plus and Joint Deconvolution (jDCV), using a dedicated computer workstation. LSM Plus uses a Wiener filter to enhance signal noise, improve resolution, and provide spatial information. jDCV works alongside the Airyscan 2 detector to add additional structural information and further improve resolution. The system uses an Axiocam 705 mono, which provides high-resolution monochrome image capture, low light fluorescence imaging, high frame rate imaging, and broad spectral sensitivity from UV to near-IR light. The microscope is equipped with a motorized stage suitable for tiling of large areas and a Z piezo stage to generate Z-stacks with precision. For multi-day, multi-position time-lapses, the system utilizes Definite Focus 3 to compensate for focus drift, resulting in sharp, high-contrast images. An opaque, integrated incubation module creates stable temperature conditions when imaging temperature-sensitive samples and eliminates the effects of potential ambient light. The objectives include EC-Plan NEO 2.5X 0.085 NA; Plan-APO 10X 0.45 NA; Plan-APO 20X 0.8 NA; Plan-APO 40X 0.95 NA; C-APO 40X 1.2 NA W; Plan-APO 63X 1.4 NA Oil. The purchase of the Zeiss 900 LSM for the Advanced Imaging and Microscopy Core Facility in the School of Medicine was made possible due to the support of NIH S10OD034427.
Capabilities
- βsuper-resolution imaging
- βhigh-contrast images
- βminimizing light exposure
- βreducing photobleaching
- βchannel bleed-through reduction
- βlight emission at 405 nm, 488 nm, 561 nm, and 640 nm
- βrapid confocal imaging
- βspatial and temporal recordings
- βmosaic tiling for multidimensional reconstruction
- βdeconvolution using LSM Plus and Joint Deconvolution (jDCV)
- βhigh-resolution monochrome image capture
- βlow light fluorescence imaging
- βhigh frame rate imaging
- βbroad spectral sensitivity from UV to near-IR light
- βtiling of large areas
- βZ-stacks with precision
- βmulti-day, multi-position time-lapses
- βfocus drift compensation
- βstable temperature conditions
- βobserving cell signaling
- βin-situ hybridization
- βprotein expression and localization
- βinteractions between molecules and proteins
- βspatial reconstruction
- βspatial-temporal relationships
- βsubcellular transport



