This shows you the differences between two versions of the page.
Both sides previous revision Previous revision Next revision | Previous revision Next revision Both sides next revision | ||
zeiss_lsm_880 [2016/04/04 16:43] bioimaging |
zeiss_lsm_880 [2022/09/01 11:46] bioimaging |
||
---|---|---|---|
Line 1: | Line 1: | ||
<html> | <html> | ||
- | <img src="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_name.jpg"> | + | <img src="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_name_new.png"> |
<table style="border:0px solid white;"> | <table style="border:0px solid white;"> | ||
<tr style="border:0px solid white;"> | <tr style="border:0px solid white;"> | ||
<td style="border:0px solid white;"> | <td style="border:0px solid white;"> | ||
- | <a href="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_wiki.jpg"><img src="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_wiki.jpg" width=300></a> | + | <a href="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_wiki_2022.png"><img src="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_wiki_2022.png" width=300></a> |
<td style="border:0px solid white;"> <p style="line-height:1.8"> | <td style="border:0px solid white;"> <p style="line-height:1.8"> | ||
- | <b>Location</b>: <a href="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_map.jpg">Room P2-A-22</a> (<img src="/facility/bioimaging/lib/exe/fetch.php?media=telephone_icon.gif" width=15> 47217) <br> | + | <b>Location</b>: <a href="/facility/bioimaging/lib/exe/fetch.php?media=zeiss_lsm_880_map_new.png">Room P2-A-22</a> (<img src="/facility/bioimaging/lib/exe/fetch.php?media=phone_neg.png" width=15> 47217) <br> |
<b>Manufacturer</b>: <a href="http://www.zeiss.de/micro" target="_blank">Carl Zeiss MicroImaging</a><br> | <b>Manufacturer</b>: <a href="http://www.zeiss.de/micro" target="_blank">Carl Zeiss MicroImaging</a><br> | ||
- | <b>Model</b>: <a href="http://www.zeiss.com/microscopy/en_de/products/confocal-microscopes/lsm-880-with-airyscan-.html" target="_blank">LSM 880 with Airyscan</a><br> | + | <b>Model</b>: <a href="https://www.youtube.com/watch?v=sGTNBXq8omg">LSM 880 with Airyscan</a> (click for Zeiss webinar) <br> |
- | <b>Software</b>: ZEN 2.1 (black) <br> | + | <b>Nickname</b>: "880"<br> |
+ | <b>Software</b>: ZEN 2.3 SP1 (black edition) <br> | ||
<b>Year</b>: 2016 <br> | <b>Year</b>: 2016 <br> | ||
<b>SN</b>: 2811000267 <br> | <b>SN</b>: 2811000267 <br> | ||
Line 15: | Line 16: | ||
  <br> |   <br> | ||
  <br> |   <br> | ||
- | → <a href="https://imm.medicina.ulisboa.pt/intranet/booking/resource_admin.php?resourcepage=0&rid=128"><img src="/facility/bioimaging/lib/exe/fetch.php?media=date.png"> Zeiss LSM 880 Booking</a> | + |   <br> |
- | <br> | + | |
→ <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_880_quality"><img src="/facility/bioimaging/lib/exe/fetch.php?media=list-icon.png" width=18> Zeiss LSM 880 Quality Control</a> | → <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_880_quality"><img src="/facility/bioimaging/lib/exe/fetch.php?media=list-icon.png" width=18> Zeiss LSM 880 Quality Control</a> | ||
<br> | <br> | ||
→ <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_880_usage"><img src="/facility/bioimaging/lib/exe/fetch.php?media=chart_line.png"> Zeiss LSM 880 Usage Statistics</a> | → <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_880_usage"><img src="/facility/bioimaging/lib/exe/fetch.php?media=chart_line.png"> Zeiss LSM 880 Usage Statistics</a> | ||
- |   </br> | ||
- | → <a href="/facility/bioimaging/doku.php?id=zeiss_lsm_880_repair"><img src="/facility/bioimaging/lib/exe/fetch.php?media=repair-icon.gif" width=16> Zeiss LSM 880 Repair History</a> | ||
</p> | </p> | ||
</td> | </td> | ||
Line 30: | Line 28: | ||
===== Microscope overview ===== | ===== Microscope overview ===== | ||
- | The Zeiss LSM 7 Live //confocal line-scanning microscope// is a fast imaging system able to analyze high-speed processes with a time resolution of just a few microseconds. It is an upright microscope equipped with water dipping objectives specially suited for live samples in aqueous media. The scanning unit uses a laser beam with a rectangular cross-section to [[http://www.nature.com/nmeth/journal/v3/n11/thumbs/nmeth971-F2.jpg|illuminate a whole line in the sample]], instead of a single point. This makes image acquisition by its array CCD detectors faster than conventional PMT light detection but it also lowers the Z-resolution due to the usage of slits instead of conventional pinholes. Note that the system is equipped with two lasers (488 and 561 nm) but dual color imaging is not advised since there are no bandpass filters in the system (channel crosstalk is likely to occur). A UV laser controlled by galvanometric mirrors is available for precise ablation in user-defined regions of interest. The spatial resolution of this system is not as high as a //point-scanning confocal system// such as the [[zeiss_lsm_880|Zeiss LSM 880]] or [[zeiss_lsm_710|Zeiss LSM 710]] but it is much faster than these two systems, achieving scanning speeds which may be even higher than the [[3i_marianas_sdc|3i Marianas SDC]] spinning disk if the acquisition is performed only in a few lines. If your personal computer cannot handle all the data you collected, check out the [[big_guy|Big Guy]] or [[colossus|Colossus]]. | + | {{ :confocal_pinhole.png?350}} The Zeiss LSM 880 with Airyscan is a point-scanning confocal microscope able to generate high-resolution three-dimensional images of thick specimens with high sensitivity, high speed and low photodamage. It is an inverted microscope especially suitable for live cell imaging and photobleaching experiments, equipped with a large cage incubator and a stage top incubator for temperature control and CO2 supply and with Definite Focus for hardware focus control during long time-lapse acquisitions. The stage is motorized and furthermore equipped with a piezo for Z displacement so fast 4D imaging is possible in multiple stage positions. Its [[http://www.zeiss.com/content/dam/Microscopy/Products/laser-scan/LSM%20880/zeiss-lsm880-airyscan-principle-672.jpg|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). It can also be used in [[https://www.youtube.com/watch?v=ln6VUmLzLLc|Fast Mode]], which enables parallel excitation and detection of four image pixels. The result is a speed improvement by a factor of four, while maintaining the sensitivity of Airyscan and 1.5x resolution improvement. Its scanning unit further includes two PMT detectors (one of them cooled) as well as a GaAsP detector for increased sensitivity (45% QE compared to ~25% QE for conventional PMT). It is equipped with lasers from violet to far red (405, 458, 488, 514, 561, 594 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|Zeiss Cell Observer]]. Image resolution with Airyscan is higher than the [[zeiss_lsm_710|Zeiss LSM 710]] and detection sensitivity is also higher than the spinning disks [[3i_marianas_sdc|3i Marianas SDC]] and [[zeiss_cell_observer_sd|Zeiss Cell Observer SD]]. If your personal computer cannot handle all the data you collected, check out the [[colossus|Colossus]]. |
- | {{info.gif?|}} **If you are going to use the 561 nm laser please write '561' in the Event Field name** | + | {{ ::fast_airyscan.png?600 }} |
- | ===== System components ===== | + | {{:info.png?25|}} Click [[https://imm.medicina.ulisboa.pt/facility/bioimaging/lib/exe/fetch.php?cache=&media=airyscan.jpg|here]] to see the system beam path in detail |
- | ==== LASERs ==== | + | {{: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. |
- | ^ Laser Unit ^ Wavelength ^ Maximum Power ^ Current Status ^ | + | |
- | | Sapphire 488-100 | 488 nm | 100 mW | ok | | + | |
- | | DPSS 561-40 | 561 nm | 40 mW | ok | | + | |
- | ==== Objectives ==== | + | ===== Additional information ===== |
- | ^ 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=440039-0000-000|W Achroplan Ph1]] | Water dipping | 0.30 | 3.1 | | + | |
- | | 10x | [[https://www.micro-shop.zeiss.com/?s=2065696c9e13e&l=en&p=uk&f=o&a=v&m=s&id=440330-0000-000|Plan-Neofluar]] | Dry | 0.30 | 5.5 | | + | |
- | | 20x | [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=421452-9900-000|W Plan-Apochromat]] | Water | 1.00 | 1.8 | | + | |
- | | 40x | [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=440090-9901-000|W Achroplan]] | Water dipping | 0.80 | 3.6 | | + | |
- | | 40x | [[https://www.micro-shop.zeiss.com/?s=3407786617d462&l=en&p=uk&f=o&a=v&m=s&id=440451-9903-000|Plan-Neofluar Ph3]] | Oil | 1.30 | 0.20 | | + | |
- | ==== Filtersets (Ocular) ==== | + | * [[https://www.youtube.com/watch?v=sGTNBXq8omg|ZEISS Webinar: LSM 880 with Airyscan - Revolutionize Your Confocal Imaging (video)]] |
+ | * [[https://www.youtube.com/watch?v=VuxgaKDa_DU|ZEISS Webinar: Fast Mode for ZEISS LSM 880 with Airyscan (video)]] | ||
- | ^ Position ^ Filterset ^ Reference ^ Excitation ^ Emission ^ | + | ===== Booking Rules ===== |
- | | 2 | Green | [[https://www.micro-shop.zeiss.com/?s=163176628fcf844&l=en&p=us&f=f&a=v&b=f&id=488010-9901-000&o=|FS10]] | 450-490 nm | 515-565 nm | | + | - **Users** can book at maximum **8 hours per week** |
- | | 3 | Red | [[https://www.micro-shop.zeiss.com/?s=163176628fcf844&l=en&p=us&f=f&a=v&b=f&id=488015-0000-000&o=|FS15]] | 540-552 nm | > 590 nm | | + | - This usage restriction does not apply for **weekends** and for working days **before 9:00** and **after 21:00** |
- | | 4 | Blue (for ablation*) | [[https://www.micro-shop.zeiss.com/?s=163176628fcf844&l=en&p=us&f=f&a=v&b=f&id=488049-9901-000&o=|FS49]] | none | 420-470 nm | | + | - Exceptions to these rules require **approval from [[joserino@medicina.ulisboa.pt|José Rino]]**. |
- | * Excitation filter has been removed | + | |
- | ==== Filter and Dichroic sets ==== | + | ===== System components ===== |
- | | {{zeiss5livefilters0.jpg?100}} | {{zeiss5livefilters1.jpg?100}} | | + | |
- | | Main configuration | Emission filters | | + | |
- | ===== Microscope Turn On Procedures ===== | + | ==== LASERs ==== |
+ | ^ Laser Unit ^ Wavelength ^ Maximum Power ^ | ||
+ | | Diode 405-30 | 405 nm | 30 mW | | ||
+ | | Argon | 458, 488 and 514 nm | 25 mW | | ||
+ | | DPSS 561-20 | 561 nm | 20 mW | | ||
+ | | HeNe594 | 594 nm | 2 mW | | ||
+ | | HeNe633 | 633 nm | 5 mW | | ||
- | ==== Normal Operation ==== | + | ==== Objectives ==== |
+ | ^ Magnification ^ Model ^ Immersion ^ NA ^ WD (mm) ^ Reference ^ | ||
+ | | 10x | EC Plan-Neofluar | Air | 0.30 | 5.20 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/420340-9901-000/Objective-EC-Plan-Neofluar-10x-0.30-M27|420340-9901-000]] | | ||
+ | | 20x | Plan-Apochromat | Air | 0.80 | 0.55 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/420650-9901-000/Objective-Plan-Apochromat-20x-0.8-M27|420650-9901-000]] | | ||
+ | | 40x | C-Apochromat Corr | Water | 1.20 | 0.28 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/421767-9970-000/Objective-C-Apochromat-40x-1.20-W-Corr-M27|421767-9970-000]] | | ||
+ | | 40x | LD C-Apochromat Corr | Water | 1.10 | 0.62 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/421867-9970-000/Objective-LD-C-Apochromat-40x-1.1-W-Corr-M27|421867-9970-000]] | | ||
+ | | 63x | Plan-Apochromat DIC | Oil | 1.40 | 0.19 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/420782-9900-799/Objective-Plan-Apochromat-63x-1.4-Oil-DIC-M27|420782-9900-799]] | | ||
- | * The system must be turned on **30 min** before usage. | ||
- | * To start it turn on the two main switches: ''SYSTEM/PC'' and ''COMPONENTS'' | ||
- | {{7live_switches.jpg?100|}} | ||
- | * 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). | ||
- | {{7live_excite.jpg?100|}} | ||
- | * You may now start using the system. | ||
- | ==== Live Imaging / Time Lapse Operation ==== | + | **Upon request:** |
- | * The system must be turned on **2 hours** before usage (in order to properly warm up scanning mirrors). | + | ^ Magnification ^ Model ^ Immersion ^ NA ^ WD (mm) ^ Reference ^ |
- | * To start it turn on the two main switches: **SYSTEM/PC** and **COMPONENTS** | + | | 25x | LCI Plan-Neofluar Corr DIC | Oil/Glyc/W | 0.80 | 0.21 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/420852-9973-000/Objective-LCI-Plan-Neofluar-25x-0.8-Imm-Corr-DIC-M27|420852-9972-000]] | |
- | * Login to the computer, wait for the network icon to change to ''connected'' state | + | | 40x | Plan-Apochromat Corr | Dry | 0.95 | 0.25 | [[https://www.micro-shop.zeiss.com/en/de/shop/objectives/420660-9970-000/Objective-Plan-Apochromat-40x-0.95-Corr-M27|420660-9970-000]] | |
- | * Start the **ZEN 2009** software. | + | ==== Filtersets (Ocular) ==== |
- | **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 ===== | + | ^ Position ^ Filterset ^ Reference ^ Excitation ^ Dichroic ^ Emission ^ |
- | If there's another user for this microscope in the next two hours: | + | | 1 | Green | [[https://www.micro-shop.zeiss.com/?s=7139069fdc79c&l=en&p=us&f=f&a=v&b=f&id=489038-9901-000&o=|FS38HE]] | 450-490 nm | 495 nm | 500-550 nm | |
- | * Exit the **ZEN 2009** software, leave the lasers on and log off the computer. | + | | 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 nm | 570-640 nm | |
- | * Clean up immersion objectives. | + | | 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 | 395 nm | 420-470 nm | |
- | * **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: ===== | + | ===== Microscope Turn On Procedure ===== |
+ | * Turn on the ''MAIN SWITCH'' | ||
+ | {{zeiss_lsm_880_1.jpg?100}} | ||
+ | * Turn on the ''SYSTEMS/PC'' switch | ||
+ | * Turn on the computer | ||
+ | * Login in to Windows (Bioimaging User) | ||
+ | * Turn on the ''COMPONENTS'' switch | ||
+ | * Start the **ZEN Black** software | ||
- | * Please contact the [[about|Bioimaging Facility]] (Ext: 47316). The ablation system requires specific training even for users that are already trained on the LSM 7 Live itself. | + | ===== Microscope Turn Off Procedure ===== |
+ | If there is another user for this microscope in the __next hour__: | ||
+ | * Exit the ZEN software, leave the lasers on | ||
+ | * Log off the computer | ||
+ | * Clean up immersion objectives | ||
+ | Else: | ||
+ | * Turn off the lasers on **ZEN** | ||
+ | * Clean up immersion objectives | ||
+ | * Exit the ZEN software | ||
+ | * Shutdown the computer | ||
+ | * Turn off the two switches ''SYSTEMS/PC'' and ''COMPONENTS'' | ||
+ | * **Wait 5 min. for Ar laser to cool down** | ||
+ | * Turn off the ''MAIN SWITCH'' | ||
---- | ---- | ||
- | + | [[resources|Back to the Equipment page]] | |
- | [[resources|Back to the Resources page]] | + |