User Tools

Site Tools


zeiss_lsm_900

Differences

This shows you the differences between two versions of the page.

Link to this comparison view

Both sides previous revision Previous revision
Next revision
Previous revision
zeiss_lsm_900 [2025/01/13 10:28]
bioimaging [Microscope Turn On Procedure]
zeiss_lsm_900 [2025/07/31 12:41] (current)
bioimaging
Line 10: Line 10:
 <​b>​Model</​b>:​ <a href="​https://​www.zeiss.com/​microscopy/​en/​products/​light-microscopes/​confocal-microscopes/​lsm-900-with-airyscan-2.html">​LSM 900 with Airyscan 2</​a><​br>​ <​b>​Model</​b>:​ <a href="​https://​www.zeiss.com/​microscopy/​en/​products/​light-microscopes/​confocal-microscopes/​lsm-900-with-airyscan-2.html">​LSM 900 with Airyscan 2</​a><​br>​
 <​b>​Nickname</​b>:​ "​900"<​br>​ <​b>​Nickname</​b>:​ "​900"<​br>​
-<​b>​Software</​b>: ​Zen 3.5<br>+<​b>​Software</​b>: ​ZEN 3.12<br>
 <​b>​Year</​b>: ​ 2022<​br>​ <​b>​Year</​b>: ​ 2022<​br>​
-<​b>​SN</​b>: ​ <br>+<​b>​SN</​b>: ​2901000180<br>
 &nbsp <br> &nbsp <br>
 Data will be deleted after: <b>1 month</​b>​ Data will be deleted after: <b>1 month</​b>​
Line 33: Line 33:
   * **LED Illumination**:​ [[https://​www.zeiss.com/​microscopy/​en/​products/​accessories/​colibri.html|Zeiss Colibri 7]]   * **LED Illumination**:​ [[https://​www.zeiss.com/​microscopy/​en/​products/​accessories/​colibri.html|Zeiss Colibri 7]]
   * **Features**   * **Features**
-    * |  [[https://​www.imdik.pan.pl/​images/​Us%C5%82ugi_dokumenty/​Przydatne_informacje/​2d_Definite_Focus_information.pdf|Definite Focus.3]]+    * | [[https://​www.imdik.pan.pl/​images/​Us%C5%82ugi_dokumenty/​Przydatne_informacje/​2d_Definite_Focus_information.pdf|Definite Focus.3]]
     * | [[https://​www.youtube.com/​watch?​v=tUiEa7vcggQ|Airyscan 2 Multiplex]]     * | [[https://​www.youtube.com/​watch?​v=tUiEa7vcggQ|Airyscan 2 Multiplex]]
     * | [[https://​www.zeiss.com/​microscopy/​en/​about-us/​newsroom/​press-releases/​2021/​zeiss-lsm-plus-and-zeiss-airyscan-joint-deconvolution.html|LSM Plus]]     * | [[https://​www.zeiss.com/​microscopy/​en/​about-us/​newsroom/​press-releases/​2021/​zeiss-lsm-plus-and-zeiss-airyscan-joint-deconvolution.html|LSM Plus]]
Line 39: Line 39:
  
 <​html>​ <​html>​
-<p align="​center"><​iframe width="​420"​ height="​236"​ src="​https://​www.youtube.com/​watch?v=odXtaRLHhIQ"​ title="​YouTube video player"​ frameborder="​0"​ allow="​accelerometer;​ autoplay; clipboard-write;​ encrypted-media;​ gyroscope; picture-in-picture"​ allowfullscreen></​iframe></​p>​+<p align="​center"><​iframe width="​420"​ height="​236"​ src="​https://​www.youtube.com/​embed/odXtaRLHhIQ"​ title="​YouTube video player"​ frameborder="​0"​ allow="​accelerometer;​ autoplay; clipboard-write;​ encrypted-media;​ gyroscope; picture-in-picture"​ allowfullscreen></​iframe></​p>​
 </​html>​ </​html>​
  
  
-{{:​warning.png?​25|}} Data files older than **1 month** will be automatically deleted on this system, please copy your data to the iMM server using the desktop link.+{{:​warning.png?​25|}} Data files older than **1 month** will be automatically deleted on this system, please copy your data to the GIMM server using the desktop link.
  
  
Line 74: Line 74:
  
  
-==== Filterset ​====+==== Emission Filters ​====
  
-^  ​Position ​ ​^  ​Filterset ​ ​^ ​ Reference ​ ^  ​Excitation ​  Dichroic ​  Emission ​ ^ +^  ​Filter name  ​^  ​Transmission(nm) ​ ​^ ​ Reference ​ ^ 
-      |  |  |  |  | + BFP   450/​40 ​ | [[https://​www.fpbase.org/​spectra/?​s=2666,​2668,​2667,​2055&​showY=0&​showX=1&​showGrid=0&​areaFill=1&​logScale=0&​scaleEC=0&​scaleQY=0&​shareTooltip=1&​palette=wavelength|96 HE]] | 
-===== Microscope Turn On Procedure ​=====+ GFP  |  425/​50 ​ | [[https://​www.fpbase.org/​spectra/?​s=1484,​1495,​1485,​2057&​showY=0&​showX=1&​showGrid=0&​areaFill=1&​logScale=0&​scaleEC=0&​scaleQY=0&​shareTooltip=1&​palette=wavelength|38 HE]] | 
 + Alexa 546  ​ ​LP590  ​[[https://​www.fpbase.org/​spectra/?​s=1530,​1533,​1536,​2059&​showY=0&​showX=1&​showGrid=0&​areaFill=1&​logScale=0&​scaleEC=0&​scaleQY=0&​shareTooltip=1&​palette=wavelength|15]] | 
 +|  Cy5  ​| ​ ​690/​50 ​ ​| ​[[https://​www.fpbase.org/​spectra/?​s=1547,​1550,​1543,​2068&​showY=0&​showX=1&​showGrid=0&​areaFill=1&​logScale=0&​scaleEC=0&​scaleQY=0&​shareTooltip=1&​palette=wavelength|50]] | 
 +|  DIC  ​| ​ <​800 ​ | - 
 +|  mPlum  |  629/​62 ​ | [[https://​www.fpbase.org/​spectra/?​s=2620,​2618,​2619,​2069&​showY=0&showX=1&​showGrid=0&​areaFill=1&​logScale=0&​scaleEC=0&​scaleQY=0&​shareTooltip=1&​palette=wavelength|64 HE]] | 
 +|  Quad  |  425/​514/​592/​709 ​ | [[https://​www.fpbase.org/​spectra/?​s=2657,​2601,​2602,​2658,​2577&​showY=0&​showX=1&​showGrid=0&​areaFill=1&​logScale=0&​scaleEC=0&​scaleQY=0&​shareTooltip=1&​palette=wavelength|90 HE]] |
  
-  ​* Turn on the ''​Laser Key''​+===== How to start your session ===== 
 + 
 +The system should be always on, you only need to: 
 +  * If incubation is needed (turn on 30 mins before acquiring):​ 
 +    ​* Turn the powerbar off 
 +{{::​Oeiras_LSM900_powerbar.png?​300|}} 
 +    * Turn the incubation controller ​on 
 +{{::​Oeiras_LSM900_incubation.png?​300|}} 
 +    * Turn the powerbar on 
 +  * Log into Windows with your Agendo credentials 
 +  * Start **ZEN** 
 + 
 +===== How to end your session ===== 
 + 
 +If there is another user for this microscope in the __next hour__: 
 +  * Exit ZEN, leave the lasers on 
 +  * Log off the computer 
 +  * Clean up immersion objectives (gently wipe with optic cleaning paper and EtOH embedded paper) 
 +Else: 
 +  * Turn off the lasers in **ZEN** 
 +  * Clean up immersion objectives (gently wipe with optic cleaning paper and EtOH embedded paper) 
 +  * Exit ZEN 
 +  * Log off the computer 
 + 
 +===== Microscope Turn On Procedure (after complete shutdown) ===== 
 + 
 +If the system is completely off, please follow this procedure:​ 
 + 
 +  * Turn the Laser key
 {{::​oeiras_900_turningon1.jpg?​300|}} {{::​oeiras_900_turningon1.jpg?​300|}}
-  * Turn on the ''​System ​and Components'' ​switch+  * Turn on the ''​SYSTEM'' ​and ''​COMPONENTS''​ switches
 {{::​oeiras_900_turningon2.jpg?​300|}} {{::​oeiras_900_turningon2.jpg?​300|}}
-  * Turn on the ''​Power bar''​ +  * Turn on the ''​Power bar'' ​(on the back right-hand side of the microscope) 
-{{::oeiras_900_turningon3.jpg?300|}}+{{::oeiras_lsm900_powerbar.png?300|}}
   * Turn on the computer   * Turn on the computer
   * Log into Windows with your Agendo credentials   * Log into Windows with your Agendo credentials
   * Start the **ZEN** software   * Start the **ZEN** software
  
 +===== Microscope Turn Off Procedure (for complete shutdown) =====
 +
 +Please only shutdown the system if instructed to do so by the Bioimaging staff.
 +
 +  * Turn off the lasers in **ZEN**
 +  * Exit ZEN
 +  * Shutdown the computer
 +  * Turn off the ''​Power Bar''​ (on the back right-hand side of the microscope)
 +  * Turn off the ''​SYSTEM''​ and ''​COMPONENTS''​ switches
 +  * Turn off the Laser key
  
 ---- ----
 +
 [[resources|Back to the Equipment page]] [[resources|Back to the Equipment page]]
zeiss_lsm_900.1736760502.txt.gz · Last modified: 2025/01/13 10:28 by bioimaging