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zeiss_lsm_880

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Location: Room P2-A-22 ( 47217)
Manufacturer: Carl Zeiss MicroImaging
Model: LSM 880 with Airyscan
Software: ZEN 2.1 (black)
Year: 2016
SN: 2811000267
 
 
 
Zeiss LSM 880 Booking
Zeiss LSM 880 Quality Control
Zeiss LSM 880 Usage Statistics  
Zeiss LSM 880 Repair History

Microscope overview

The Zeiss LSM 880 with Airyscan is a confocal point-scanning microscope able to generate high-resolution three-dimensional images of thick specimens with high sensitivity and low photodamage. It is an inverted microscope specially suitable for live cell imaging and photobleaching experiments, equipped with a large size incubator for temperature control and CO2 supply. Its Airyscan 32 channel area detector is able to collect all light from an Airy pattern simultaneously, allowing for increased resolution (140 nm laterally and 400 nm axially, at 488 nm). Its scanning unit further includes two PMT detectors (one of them cooled for single photon counting) as well as a GaAsP detector. It is equipped with lasers from violet to far red (405, 458, 488, 561 and 633 nm excitation wavelengths). With this system you can perform optical sectioning of fluorescent samples which are too thick for a widefield system such as the Zeiss Axiovert 200M. Image resolution and detection sensitivity are higher than faster confocal systems such as a spinning disk or the Zeiss LSM 7 Live, but image acquisition is slower. If you need to use a 594 nm laser or a 40x water objective for higher working distances, check the Zeiss LSM 510 META confocal point-scanning system. If your personal computer cannot handle all the data you collected, check out the Big Guy.

System components

LASERs

Laser Unit Wavelength Maximum Power Current Status
Sapphire 488-100 488 nm 100 mW ok
DPSS 561-40 561 nm 40 mW ok

Objectives

Magnification Model Type NA WD (mm)
10x W Achroplan Ph1 Water dipping 0.30 3.1
10x Plan-Neofluar Dry 0.30 5.5
20x W Plan-Apochromat Water 1.00 1.8
40x W Achroplan Water dipping 0.80 3.6
40x Plan-Neofluar Ph3 Oil 1.30 0.20

Filtersets (Ocular)

Position Filterset Reference Excitation Emission
2 Green FS10 450-490 nm 515-565 nm
3 Red FS15 540-552 nm > 590 nm
4 Blue (for ablation*) FS49 none 420-470 nm

* Excitation filter has been removed

Filter and Dichroic sets

zeiss5livefilters0.jpg zeiss5livefilters1.jpg
Main configuration Emission filters

Microscope Turn On Procedures

Normal Operation

  • The system must be turned on 30 min before usage.
    • To start it turn on the two main switches: SYSTEM/PC and COMPONENTS

  • Login to the computer, wait for the network icon to change to connected state
  • Start the ZEN 2009 software.

After the 30 min:

  • Turn on the metal halide lamp (white box to the left of the microscope).

  • You may now start using the system.

Live Imaging / Time Lapse Operation

  • The system must be turned on 2 hours before usage (in order to properly warm up scanning mirrors).
    • To start it turn on the two main switches: SYSTEM/PC and COMPONENTS
  • Login to the computer, wait for the network icon to change to connected state
  • Start the ZEN 2009 software.

After the 2 hours:

  • Turn on the metal halide lamp (white box to the left of the microscope).
  • You may now start using the system.

Microscope Turn Off procedures

If there's another user for this microscope in the next two hours:

  • Exit the ZEN 2009 software, leave the lasers on and log off the computer.
  • Clean up immersion objectives.
  • Make sure that there really is another user going to use the microscope.

Else:

  • Turn off the lasers, wait 5 min for them to cooldown.
  • Exit the ZEN 2009 software and shut down the computer.
  • Clean up immersion objectives.
  • Turn off the metal halide lamp.
  • Turn off the microscope.
  • Turn off the two main switches: SYSTEM/PC and COMPONENTS

If you want to use the UV laser ablation system:

  • Please contact the Bioimaging Facility (Ext: 47316). The ablation system requires specific training even for users that are already trained on the LSM 7 Live itself.

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zeiss_lsm_880.1459781963.txt.gz ยท Last modified: 2016/04/04 16:59 by bioimaging