Bioimaging Wiki

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<a href="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_710_wiki.jpg"><img src="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_710_wiki.jpg" width=300></a>
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<b>Location</b>: <a href="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_710_map.jpg">Room P3-A-10</a> (<img src="/facility/bioimaging/lib/exe/fetch.php?media=telephone_icon.gif" width=15> 47311) <br> 
<b>Manufacturer</b>: <a href="http://www.zeiss.de/micro" target="_blank">Carl Zeiss MicroImaging</a><br>
<b>Model</b>: LSM 710<br>
<b>Software</b>: ZEN 2012<br>
<b>Year</b>: 2010 <br>
<b>SN</b>: 2503000400 <br>
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&rarr; <a href="http://www.imm.fm.ul.pt/booking/month.php?user=ZEISSLSM7&rid=51"><img src="/facility/bioimaging/lib/exe/fetch.php?media=date.png">  Zeiss LSM 710 Booking</a>
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&rarr; <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_710_quality"><img src="/facility/bioimaging/lib/exe/fetch.php?media=list-icon.png" width=18> Zeiss LSM 710 Quality Control</a>
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&rarr; <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_710_usage"><img src="/facility/bioimaging/lib/exe/fetch.php?media=chart_line.png">  Zeiss LSM 710 Usage Statistics</a>
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&rarr; <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_710_repair"><img src="/facility/bioimaging/lib/exe/fetch.php?media=repair-icon.gif" width=16> Zeiss LSM 710 Repair History</a>
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===== Microscope overview =====
The Zeiss LSM 710 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 (but no stage incubator for CO2 supply). Its scanning unit has a spectral recycling loop, two sensitive PMT detectors and a filter-free spectral separation module that can be continuously set over the entire wavelength range (i.e. you can specify which wavelength range you want to detect). It is equipped with lasers from violet to far red (405, 458, 488, 514, 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_cell_observer_wf|Zeiss Cell Observer WF]] or the [[zeiss_axiovert_200m|Zeiss Axiovert 200M]]. Image resolution and detection sensitivity are higher than faster confocal systems such as the spinning disk [[3i_marianas_sdc|3i Marianas SDC]] or the [[zeiss_lsm_7_live|Zeiss LSM 7 Live]], but image acquisition is slower. If you need to use a 594 nm laser or increased resolution and sensitivity, check the [[zeiss_lsm_880|Zeiss LSM 880]] confocal point-scanning system. If your personal computer cannot handle all the data you collected, check out the [[big_guy|Big Guy]] or [[colossus|Colossus]].

===== Booking Rules =====
The Zeiss LSM 710 booking is divided in three daily slots:
|  9:00 to 13:00  |  13:00 to 17:00  |  17:00 to 21:00  |

  - A **user** can book at maximum **2 sessions per week**
  - Each **session must fit inside one of the three daily slots** (i.e. a session booked from 11:00 to 14:00 counts as 2 sessions)
  - The above rules do not apply for **weekends** and for work days **before 9:00** and **after 21:00**
  - The above rules do not apply for sessions booked on the very same day or **24 hours ahead**
  - Exceptions to these rules require **approval from [[joserino@medicina.ulisboa.pt|José Rino]]**.
  - Users must indicate which lasers they are going to use in the booking Description field
  - Users must indicate if they will use the incubator in the booking Description field (write down 37C INCUBATOR)
  - Users must write their internal extension phone number in the booking Description field

===== System components =====

==== LASERs ====
^  Laser Unit  ^  Wavelength  ^  Maximum Power  ^  Current Status  ^
|  Diode 405-30  |  405 nm  |  30 mW  |  ok  |
|  Argon  |  458, 488 and 514 nm  |  25 mW  |  ok  |
|  DPSS 561-10  |  561 nm  |  15 mW  |  ok  |
|  HeNe633  |  633 nm  |  5 mW  |  ok  |

==== Objectives ====
^  Magnification   ^  Model  ^  Type  ^  NA  ^  WD (mm)  ^
|  10x  |  [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=420340-9901-000|EC Plan-Neofluar]]  |  Dry  |  0.30  |  5.2  |
|  20x  |  [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=420650-9901-000|Plan-Apochromat]]  |  Dry  |  0.80  |  0.55  |
|  40x  |  [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=440452-9903-000|EC Plan-Neofluar]]  |  Oil  |  1.30  |  0.20  |
|  63x  |  [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=440762-9904-000|Plan-Apochromat]]  |  Oil  |  1.40  |  0.19  |

**Upon request:**

^  Magnification   ^  Model  ^  Type  ^  NA  ^  WD (mm)  ^
|  25x  |  [[https://www.micro-shop.zeiss.com/?s=129353259d52f12&l=en&p=uk&f=o&a=v&m=s&id=420852-9972-000|LCI Plan-NeoFluar]]  |  Oil/Glyc/W  |  0.8  |  0.21  |
|  100x  |  [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=440782-9902-000|Plan-Apochromat]]  |  Oil  |  1.40  |  0.17  |

==== Filtersets (Ocular) ====

^  Position  ^  Filterset  ^  Reference  ^  Excitation  ^  Emission  ^
|  1  |  Green  |  [[https://www.micro-shop.zeiss.com/?s=163176628fcf844&l=en&p=us&f=f&a=v&b=f&id=000000-1031-346&o=|FS38]]  |  450-490 nm  |  500-550 nm  |
|  2  |  Red  |  [[https://www.micro-shop.zeiss.com/?s=163176628fcf844&l=en&p=us&f=f&a=v&b=f&id=000000-1114-101&o=|FS43]]  |  533-558 nm  |  570-640 nm  |
|  3  |  Blue  |  [[https://www.micro-shop.zeiss.com/?s=163176628fcf844&l=en&p=us&f=f&a=v&b=f&id=488049-9901-000&o=|FS49]]  |  G 365 nm  |  420-470 nm  |

===== Microscope Turn On Procedure =====
  * Turn on the ''MAIN SWITCH''
  * Turn on the two switches: ''SYSTEMS/PC'' and ''COMPONENTS''
{{switches_710.jpg?100}}
  * Turn the metal halide power source on (if needed)
{{halide_710.jpg?80}}
  * Turn the Ar laser on using the key (if needed)
{{laser_key_710.jpg?100}}
  * Turn the computer on
  * Login with your unit account
  * Wait for network icon to change to ''connected'' state
  * Switch the Ar laser from ''idle'' ton ''run'' (don't change the ''current'')
{{laser_run_710.jpg?100}}
  * Start the ''ZEN 2009'' software

===== Microscope Turn Off Procedure =====
If there's another user for this microscope in the next hour:
  * Close the software, leave the lasers on an log off the computer. 
  * Clean up any objective were you used immersion oil.
  * **Make sure that there really is another user going to use the microscope.**
Else:
  * Turn off the 561 nm laser and incubator in the software (if used)
  * Switch the Ar laser from ''run'' to ''idle'' (if used)
  * Turn off the Ar laser using the key (if used)
  * Clean up any objective were you used immersion oil.
  * Exit the software, shut down the computer.
  * Turn off the metal halide lamp
  * Turn off the main switches ''SYSTEMS/PC'' and ''COMPONENTS''
  * Wait 5 min. for Ar laser cooldown
  * Turn off the ''MAIN SWITCH''.
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