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| id | Description |
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| title | Description |
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| DescriptionLight sources| Expand |
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| title | Complete specifications |
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| Emission peak (nm) | Nominal Power (mW) | Measured Power (mW)
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| 385/30 | 150 | | | 469/38 | 110 | | | 555/30 | 31 | | | 631/33 | 50 | |
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| name | Zeiss_Colibri-7_Product Information.pdf |
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| height | 250 |
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Zeiss Colibri 7 Spectra
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Objectives2.5x/0.075 Air - 10x/0.25 Air Ph1
- 20x/0.5 Air Ph2
40x/0.75 Air Ph2 - 63x/0.75 Air Ph2 Long Distance
- 63x/1.4 Oil
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| title | Complete specifications |
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| | Position | Name | Brand | Full name | ID | Magnification | Numerical Aperture | Immersion | Type | Working distance (mm) | Transmittance (% [nm]) | Technique | Cover glass thickness (mm) |
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| 1 | 2.5x/0.075 Air | Zeiss | 2.5x/0.075 EC Plan-Neofluar | 420320-9901-000 | 2.5x | 0.075 | Air | Plan Neofluar | 9.5 | >80% [400-840] | BF, Fluo | 0.17 | | 2 | 10x/0.25 Air | Zeiss | 10x/0.25 Ph1 N-Achroplan | 420941-9911-000 | 10x | 0.25 | Air | N-AchroPlan | 6.5 | Not Available | BF, PhC, Fluo | 0.17 | | 3 | 20x/0.5 Air | Zeiss | 20x/0.50 Ph2 EC Plan-Neofluar | 420351-9910-000 | 20x | 0.50 | Air | Plan Neofluar | 2.0 | Not Available | BF, PhC, Fluo | 0.17 | | 4 | | Zeiss | 40x/0.75 Ph2 EC Plan-Neofluar | 420361-9910-000 | 40x | 0.75 | | Plan Neofluar | 0.71 | Not Available | BF, PhC, Fluo | 0.17 | | 5 | 63x/0.75 Air
| Zeiss | 63x/0.75 Corr Ph2 LD Plan-Neofluar | 421381-9970-000 | 63x | 0.75 | Air | LD Plan-Neofluar | 1.7 at cover glass 0.75 | Not Available | BF, PhC, Fluo | 0 - 1.5 | | 6 | 63x/1.4 Oil | Zeiss | 63x/1.4 DIC Plan-Apochromat Oil | 420782-9900-000 | 63x | 1.4 | Oil | Plan Apochromat | 0.19 | >80% [400-700] | BF, Fluo | 0.17 |
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Filter
- DAPI
- GFP
- Rhodamine
- DHE (dihydroethidium)
- Cy5
- Quadruple DAPI/GFP/Cy3/Cy5
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| title | Complete specifications |
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Detectors- PCO Edge 5.5
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| title | Complete specifications |
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| | Camera | PCO Edge 5.5 |
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Sensor Type | sCMOS | Sensor Category
| Monochrome | Nb Pixels
| 5.5 M | Pixel Layout | 2560 x 2160 | Pixel size | 6.5 um
| Sensor size
| 16.6 mm x 14.0 mm | Sensor diameter
| 21.8 mm
| Bit depth
| 16-bit | | Speed at full resolution | 100 images/s
| Max QE
| 60 % at 600 nm | | Reading noise | 1.0 e⁻ | Cooling
| Forced air +7C | Dark Current
| 0.6 e⁻/pixel/sec | Full well capacity
| 30 000 e-
| Dynamic Range
| 1:30000 | Interface
| Dual Camera Link PCIe | Mount
| C-mount |

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| name | PCO_Edge 5.5_Datasheet.pdf |
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| height | 250 |
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- Zeiss Axiocam MRm (not installed)
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| title | Complete specifications |
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| | Camera | Zeiss Axiocam MRm |
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Sensor Type | CCD | Sensor Category
| Monochrome | Nb Pixels
| 1.4 M | Pixel Layout | 1388 x 1040 | Pixel size | 6.45 um
| Sensor size
| 8.9 mm x 6.7 mm | Sensor diameter
| 11 mm
| Bit depth
| 12-bit | | Speed at full resolution | 13 images/s
| Max QE
| 55 % | | Readout noise | 8 e⁻ | Cooling
| Pelletier | Dark Current
| 0.7 e⁻/pixel/sec | Full well capacity
| 17 000 e-
| Dynamic Range
| 1:2000 | Interface
| FireWire (IEEE 1394a) | Mount
| C-mount |

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| name | Zeiss_AxioCam MRm_Datasheet.pdf |
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| height | 250 |
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| id | User Guide |
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| title | User Guide |
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| User Guide| UI Expand |
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| - If not already done, turn on the computer (#1) and log in to Windows using your UdeM credentials
- Remove the dust cover from the microscope
- If incubation is required, turn on the incubation power bar (#2) on the desk near the computer and open the CO₂ cylinder (#2B) near the sink
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Make sure the humidifier is properly filled with distilled water. |
Turn on the microscope power bar (#3) on the desk near the computer - When using the instrument for the first time, it is necessary to import the microscope configuration before starting the software. See the First Use section below.
- Start Zen
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| When using the instrument for the first time, it is necessary to import the microscope configuration into the software. This procedure is usually carried out during the training session. However, it can also be used to reset the software if it does not display correctly, for example. Running this procedure will erase all your experiment protocols and reset the software to its original settings (ask for support if you are not sure).
If Zen is open, close it and wait until it has completely shut down (this may take up to 30 seconds) On the Desktop, open the Softwares folder Double-click Zen Settings for Zeiss Z1-Colibri A script will run and a black window will appear briefly When the message Settings for Zen have been imported successfully appears, click OK to close it You can now open Zen
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| During this procedure, you will: - Set the microscope to a safe configuration
- Perform a calibration
- Load your sample
- Find and adjust the focus
Once completed, your sample will be ready for acquisition.
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| This step is required to calibrate the microscope in XY and Z. Performing this calibration will significantly reduce the time needed to locate and focus on your sample. - If not already done, select the lowest-magnification objective. On the microscope touch screen Home > Microscope > Control > Objectives > 2.5x
- In Zen, once it has started a calibration dialog should appear. Simply click Calibrate Now.
The microscope will lower the objectives, perform an XY calibration first, followed by a Z calibration, and then return to its original position.
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Once calibrated, the focus is typically found at Z = 1.1 mm for a microscope slide. For a multi-well plate the focus is generally around Z = 3 mm but this is highly dependent on your multi-well plate. The Z position can be viewed on the microscope touch screen under Home > Z-Position, as well as in Zen within the Focus tab, located on the right side of the screen. |
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| title | The calibration dialog did not appear... |
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| The system may already be calibrated. This can occur if a previous user calibrated the system and left it on. | UI Expand |
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| title | Verifying if the system is already calibrated |
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| In Zen, within the Focus tab, located on the right side of the screen: Click Load to lower the objective - The Z position is indicated below Current
- If Z position value is less than 100 um the system is calibrated
On the microscope touch screen: Lower the objective by pressing Home > Load Position Press Set Work Position to store this position If necessary, slightly adjust the focus upward to clear the Lower Z Limit Reached message displayed on the touch screen - The Z position value is indicated
- If the value is less than 0.1 mm then the system is calibrated
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| title | Manual calibration with the software |
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| In Zen, within the Stage tab, located on the right side of the screen: - If not already done, check the Show All option
At the bottom of the tab click Calibrate A warning message will show up click Continue The microscope will lower the objectives and perform a XY stage calibration and then return to its original position.
In Zen, within the Focus tab, located on the right side of the screen: - If not already done, check the Show All option
At the bottom of the tab click Calibrate A warning message will show up click Continue The microscope will then perform a Z calibration and then return to its original position
XY and Z calibrations are now complete |
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| title | Manual calibration with the microscope touch screen |
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| On the microscope touch screen: Navigate to Home > Microscope > XYZ > Position > Z-Position > Set Zero > Auto to perform focus calibration Press OK to start the calibration procedure Wait a few seconds for the calibration to complete Lower the objective by pressing Home > Load Position Press Set Work Position to store this position If necessary, slightly adjust the focus upward to clear the Lower Z Limit Reached message displayed on the touch screen Navigate to Home > Microscope > XYZ > Position > XY-Position > Set Zero > Auto to perform a stage calibration Press OK to start the calibration procedure Wait a few seconds for the calibration to complete
XY and Z calibrations are now complete |
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| title | Ensuring the calibration dialog is displayed at startup |
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| In Zen: In the menu bar, navigate to Tools > Options Select Startup/Shutdown Under Stage/Focus Calibration, ensure Request Stage/Focus Calibration on Startup is checked Click OK to close the Options dialog
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| | Warning |
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| | Ensure that the calibration has been completed beforehand. Calibration will significantly reduce the time required to locate and focus on your sample. |
On the microscope touch screen: - If not already done, select the lowest-magnification objective Home > Microscope > Control > Objectives > 2.5x
| Info |
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The 2.5× and 10× objectives are the safest to use due to their long working distance (>6 mm). The sample will appear in sharp focus well before the objective approaches it. It is recommended to always focus using the safest objectives first. Since the objectives are parafocal, focusing with the safest objectives will facilitate locating the sample when switching to higher-magnification objectives.
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Lower the objective by pressing Home > Load Position Press Set Work Position to store this position If necessary, slightly adjust the focus upward to clear the Lower Z Limit Reached message displayed on the touch screen - Place the test slide on the microscope stage with the coverslip facing the objective
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| Using a test slide will significantly reduce the time required to set up the instrument. |
- If necessary, adjust the stage to ensure that the sample is centred under the objective
In Zen: - In the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP, Cy3, Cy5) to activate the configuration
- Adjust the focus with the main dial while looking through the eyepieces until the image is perfectly sharp
| Info |
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Once calibrated, the focus is typically found at Z = 1.1 mm for a microscope slide. For a multi-well plate the focus is generally around Z = 3 mm but this is highly dependent on your multi-well plate. The Z position can be viewed on the microscope touch screen under Home > Z-Position, as well as in Zen within the Focus tab, located on the right side of the screen. |
- In the Locate tab, select Off to turn off the illumination
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| | Warning |
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| Perform the initial focus using the safest objective before switching to higher-magnification objectives. |
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| title | Focusing with air objectives |
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| After performing the initial focus, on the microscope touch screen: - Press Home>Microscope>Control>Objectives
- Press 10x, 20x, 40x or 63x (0.75) to select the desired objective
| Info |
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The 40x objective is the best Air objective because it has the largest Numerical aperture (0.75) together with a wider field of view (40x).
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In Zen: - In the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP, Cy3, DsRed, Cy5) to activate the configuration
- Adjust the focus with the precision dial while looking through the eyepieces until the image is perfectly sharp
- In the Locate tab, select Off to turn off the illumination
Your sample is ready for acquisition! |
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| title | Focusing with oil objectives |
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| After performing the initial focus, on the microscope touch screen:
- Press Home>Microscope>Turret>Objectives
Press 63x Oil (1.4)to select the desired objective. The microscope will automatically lower the stage so that the sample becomes accessible.
- Place a single drop of oil on the objective
- Press Done. The microscope will automatically return the objective to its original position
In Zen : - In the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP, Cy3, DsRed, Cy5) to activate the configuration
- Adjust the focus with the precision dial while looking through the eyepieces until the image is perfectly sharp
- In the Locate tab, select Off to turn off the illumination
Your sample is ready for acquisition! |
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| - Files can be saved temporarily (during acquisition) on the local C: drive (desktop)
- At the end of each session, copy your data to your external drive and delete it from the local C: drive
- You can store your files on the D: drive (Data Storage). If you do, please create a folder per laboratory using the principal investigator last name. Within, create one folder per user (Firstname_Lastname).
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In any case, your files should be removed from the C: drive. |
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| - Save your data
- Close Zen
- Transfer your data to the D: drive (Data Storage) or to your external drive and delete it from the local C: drive
- If used, clean oil objectives with lens cleaner and paper
- Select the lowest magnification objective and press load position to place the objectives in a safe position
If used, turn off the incubation module power strip (#2A) and close the CO2 cylinder (#2B) Turn off the microscope power bar (#3) - Turn off the computer
- Cover the instrument with the protective dust cover
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| - Take back your samples including ones in the microscope
- Leave the microscope and the working area clean
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| Tabs Page |
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| Log| UI Expand |
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| - Measure Power output
- Modify camera power supply cable
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| title | 2025-10-22 Windows 11 and more |
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| - Installation of Windows 11
- Added CO2 connection to incubation module
- Cable management
- Replaced video card
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| title | 2025-09-01 Camera upgrade |
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| - Added compressed air connexion to the anti-vibration table
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| title | 2025-09-01 Camera upgrade |
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| - AxioCam replacement with PCO Edge 5.5
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| title | 2025-08-21 Wiki Updated |
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| - Updated wiki with complete specifications
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| title | 2024-02-22 Microscope Firmware update |
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| - Microscope Firmware update to add Colibri to the touchscreen
- Zen 3.5 HotFix 10
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| - Computer replacement
- Added Colibri
- Added startup procedure
- Parafocality and paracentrality
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| - Added complete description
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| Tabs Page |
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| Technical DatasheetStandLight sources- Transmitted LED light
- Colibri 7 R(G/Y)B-UV 423052-9730-000 Serial 5440000661
CondenserObjectives2.5x/0.075 Air 420320-9901-000
10x/0.25 Air Ph1 420941-9911-000
20x/0.5 Air Ph2 420351-9910-000
40x/0.75 Air Ph2 420361-9910-000
63x/0.75 Air Ph2 Long Distance 421381-9970-000
63x/1.4 Oil 420782-9900-000
Stage- Motorized stage Marzhauser Scan IM 130x100-2mm 90-24-550-0000 Serial 16053038
Stage Controller 90-76-024-1803 Serial 14 04 1 2040 SMC 2009 432929-9011-000 - Remote control joystick 2-Axis 90-76-200-0820 Zeiss Article 432903-9011-000 Serial 1615142059
- Inserts
- Slide combo
- Multi-well plate
Filters- DAPI Filter Set 49 488049-9901
- GFP Filter Set 13 488013-0000
- Rhodamine Filter Set 43 000000-1114-101
- DHE (dihydroethidium) 424931
- Cy5 Filter Set 50 488050-9901
- Multiband FS90 HE LED 489090-9110-000
Detector- Zeiss AxioCam MRm Model: r3.1 Part Number: 426509-9901-000. Serial: 1 22 12 5537
- PCO Edge 5.5 Model pco.API.Air.BX Serial 6000001404
Workstation- Computer
- Fujitsu Esprimo P920 E90+ Model MI5W Serial YLPS036541
- Motherboard
- Fujistsu D3222-A1 (1 PCIe Gen3 x16, 1 PCIe Gen 2 x16 (x4 lanes), 2x PCIe Gen2 x1
- Chipset Intel Q87
- BIOS UEFI compatible American Trend v4.6.5.4 R1.47.0 for D3222-A1x 2019-08-26
- Processor
- Intel Core i5-4670 @ 3.4 GHz
- RAM
- 24 GB DDR3 800 MHz (3 x 8 GB)
- OS Drive
- 1 TB SSD 550 MB/s
- Win 11 23H2
- Storage
- Video Card
- AMD FirePro V4900 1 GB DDR5 0.768 TFLOPS 1x PCIe gen2 x16
- Monitor
- LG Flatron E2711 27' 1920 x 1080
- LG W2442 1920 x1080
- Software
- Zen Blue 3.5
- Serial 1121159628-524292
- HASP 1798977001
- Extended Focus
- Measurements
- Multi-Channel
- Panorama
- Software autofocus
- Time Series
- Z-stack
Incubation- Pecon stage top incubation
Anti-vibration table- TMC Model 63 512 Serial 933240
- Plain table top
ConsumablesManuals |
| Tabs Page |
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| title | Troubleshooting & FAQ |
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| Troubleshooting| UI Expand |
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| title | I don't see any fluorescence! |
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| Technical support is free and unlimited. Contact us ! |
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| title | I see a high background in fluorescence |
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| This happens in the following conditions at - At 2.5x using the DAPI or GFP channel
- At 10x using the GFP channel
- At 20x using the GFP channel
To solve this you can use any of the following option: - Tilt the transmitted light arm backward
- Close the manual shutter between the condenser and the transmitted light
- Use a higher magnification objective
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FAQ| UI Expand |
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| title | Can I use this microscope to look at cell in a dish? |
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| Yes. This is an inverted microscope designed to look at specimen in a dish or a multi-well plate. The objectives are optimized to image through thin glass bottom multi-well plates. You may also image specimen mounted between a slide and a 0.17mm thick coverslip. For long timelapse, be aware of photo-toxicity. |
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| title | Can I use this microscope to perform timelapse experiments? |
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| Yes, but... This microscope has an incubation module to maintain temperature, humidity and gas. Yet it does not have a Definite focus which can maintain focus throughout time. Therefore, it is possible to loose the focus over long period. You can always do a software autofocus at different time but be aware of photo-toxicity if you are using fluorescence.
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| title | What is Extended Depth of Focus? |
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| Extended Focus is a method to flatten a Z-stack by keeping only the relevant information. In Zen: - Select the Processing Tab
- Select the Extended Depth of Focus Method
- Click Apply
- Wait until the processing is finished
- Save the processed image
Z Stack animation Maximum Intensity projection of a Z-Stack Extended Depth of Focus projection of a Z-Stack
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