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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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Image AddedZeiss 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
| Expand |
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| title | Complete specifications |
|---|
| | Position | Name | Brand | Full name | ID | Magnification | Numerical Aperture | Immersion | Type | Working distance (mm) | Transmittance (% [nm]) | Technique | Cover glass thickness (mm) |
|---|
| 1 | 2.5x/0.075 Air | Zeiss | 2.5x/0.075 EC Plan-Neofluar | M27M27 | 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 | M27 | 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 | M27 | 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 | M27| 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 | M27 |
Filter
- DAPI
- GFP
- Rhodamine
- DHE (dihydroethidium)
- Cy5
- Quadruple DAPI/GFP/Cy3/Cy5
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| title | Complete specifications |
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| |
Detectors- Zeiss AxioCam MRm, CCD Sensor 1.4M px, 1388 x 1040 pixels, 6.45um/pixel, 12-bit, 13 images/s at full resolution, sensor size 8.8 mm x 6.6 mm (D 11 mm), Max QE 55%, Dynamic Range 1:1700
- PCO Edge 5.5 CMOS sensor 5.5 M px, 2560 x 2160 pixels, 6.5um/pixel, 16-bit, 100 images/s at full resolution, sensor size 16.6 mm x 14 mm (D 17.4 mm), Max QE 60%, Dynamic Range 1:30 000
- PCO Edge 5.5
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| title | Complete specifications |
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| | Camera | PCO Edge 5.5 |
|---|
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 |
Image Added
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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 |
Image Added
| View file |
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| name | Zeiss_AxioCam MRm_Datasheet.pdf |
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| height | 250 |
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| Tabs Page |
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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
| Note |
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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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| UI Expand |
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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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| UI Expand |
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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.
| UI Expand |
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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.
| Tip |
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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. |
| Expand |
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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
|
| UI Expand |
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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 |
| UI Expand |
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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 |
| UI Expand |
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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 |
|---|
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.
|
Lower the objective by pressing Home > Load Position
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| | Tabs Page |
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| id | User Guide |
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| title | User Guide |
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| | UI Expand |
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| - If not already done, turn on the computer (#1) and use your UdeM credentials to log in to Windows
- Remove the dust cover from the microscope
- If incubation is required turn on the incubation power bar (#2)
Turn on the microscope power bar (#3) on the desk near the computer - When using for the first time, it is necessary to import the microscope-specific parameters BEFORE starting the software. See the First Use section below.
- Start Zen
|
| UI Expand |
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| When using for the first time, it is necessary to import the microscope-specific parameters into the software. This procedure is usually carried out during the training session.However, it is also possible to use it to reset the software if it is not displayed correctly, for example.| Note |
|---|
Please note, this procedure will delete all your experiment protocols and restore the software to its original settings. |
- If open, close Zen and wait for it to close completely (up to 30 seconds)
- On the Desktop open the Softwares folder
- Double-click Zen Settings for Axio-Osberver Z1-Colibri
- A script will run and a black window will appear briefly
- Click OK to close the message Settings for Zen have been imported successfully.
- You can then open Zen
| UI Expand |
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| This procedure puts the microscope in a safe configuration and performs a calibration. At the end of this procedure the microscope will be ready for acquisition. | UI Expand |
|---|
| This step is required to calibrate the microscope in XY and Z. Doing a calibration will save you a lot of time to find your focus on your sample. | UI Expand |
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| title | Calibration within the Zen Software |
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| On the microscope touch screen: - If not already done, press Home>Microscope>Control>Objectives>2.5x to select a safe objective
In Zen: - Once Zen software is started a popup dialog should show up, just click Calibrate Now
- The microscope will lower the objectives perform a XY calibration and then a Z calibration
- Once calibrated, the focus can be found at Z = 1.1 mm for a microscope slide). The Z value can be found on the microscope touch screen Home>Z-Position
If the calibration popup dialog did not show up you at Zen opening, you can do it manually: Select the Stage window (on the right of Zen window) and click Calibrate A warning message will show up click Continue The microscope will lower the objectives perform a XY calibration
Then in the Focus Window on the right of Zen window) and click Calibrate A warning message will show up click Continue The microscope will lower the objectives perform a Z calibration Done. nce calibrated, the focus can be found at Z = 1.1 mm for a microscope slide). The Z value can be found on the microscope touch screen Home>Z-Position | UI Expand |
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| title | Calibration with the touch screen |
|---|
| On the microscope touch screen: - If not already done, Press Home>Load Position to lower the objectives to the lowest position
- Press Set Work Position to store this position
- If necessary, move the focus slightly up to remove the Lower Z limit reached message displayed on the touchscreen
- If not already done, press Home>Microscope>Control>Objectives>5x to select the 5x objective
- If asked, tap Done to remove the oil lens cleaning warning
- Press 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 be completed
- Press 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 be completed
| Note |
|---|
Once calibrated, the focus can be found at Z = 1.7 mm). The Z value can be found on the microscope touch screen Home>Z-Position |
|
| UI Expand |
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| | Warning |
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| Make sure to calibrate the focus before performing the first focus. |
On the microscope touch screen: - If not already done, press Home>Microscope>Turret>Objectives>5x to select the 5x objective
| Info |
|---|
The 5x objective is the safest because it has the longest working distance (12mm). The sample will appear perfectly sharp long before the lens approaches it. It is recommended to always first focus with the safest lens. The objectives are parafocal, focusing with the safest objective will then allow you to easily find your sample with another objective. The 10x objective is also safe because its working distance is 6.5 mm. |
- If not done already, press Home>Load Position to lower the objective to the lowest position and press Set Work Position to store this position
- If necessary, move the focus slightly up to remove the Lower Z limit reached message displayed on the touchscreen
- Place the test slide on the microscope stage with the coverslip toward the objective
| Note |
|---|
| Always use the test slide to perform the first focus. |
- If necessary, move the stage so that the sample is centered on the objective
On the computer: Open Zen In the Locate tab, select BF or the desired fluorescence (DAPI, GFP, mPlum) to activate the configurationAdjust the focus with the main dial while looking through the eyepieces until the image is perfectly sharp
| Note |
|---|
Once calibrated, the focus can be found at Z = 1.7 mm). The Z value can be found on the microscope touch screen Home>Z-Position | In the Locate tab, select Off to turn off the illumination| UI Expand |
|---|
| | Warning |
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| First focus with the safest objective before selecting another lens and continuing with secondary focus. |
| UI Expand |
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| title | Focusing with air objectives |
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| After performing the first focus, on the microscope touch screen: Press Home>Microscope>Control>Objectives, press 10x, 20x or 40x to select the desired objective| Info |
|---|
The 40x objective is the best Air objective because it has the greatest number of optical corrections (Plan Apochromat) and the largest numerical aperture (0.95) but has a smaller field of view. The 20x/0.8 objective offers the best compromise between Resolution and Field of View |
| Note |
|---|
There are two (2) 40x objectives, make sure you select the Air 40x |
In Zen : - In the Locate tab, select BF or the desired fluorescence (DAPI, GFP, mPlum) 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 the illumination off
- Your sample is ready for acquisition!
| UI Expand |
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| title | Focusing with oil objectives |
|---|
| After performing the first focus, on the microscope touch screen:
Press Home>Microscope>Turret>ObjectivesPress 63x Oil, 40x Oil to select the desired objective. The microscope will automatically lower the stage so that the sample is accessible.
| Info |
|---|
The 40x and 63x oil objectives provide the same spatial resolution because they have the same numerical aperture (1.4). The 40x oil objective offers a larger field of view and transmits light slightly better beyond 700nm. The 63x oil objective transmits light slightly better in the visible spectrum (440-710 nm) and has a better Strehl ratio (90%). It is particularly suited for super-resolution imaging, but its field of view is smaller. |
| Note |
|---|
There are two (2) 40x objectives, make sure you select the 40x Oil | Place a single drop of oil on the objectivePress Done. The microscope will automatically return the objective to its original positionIn Zen : - In the Locate tab, select BF or the desired fluorescence (DAPI, GFP, mPlum) 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 the illumination off
- Your sample is ready for acquisition!
| UI Expand |
|---|
| This procedure puts the microscope in a safe configuration and performs a focus calibration. At the end of this procedure the microscope will be ready for acquisition. | UI Expand |
|---|
| On the microscope touch screen: - Press Home>Load Position to lower the objectives to its lowest position
- Press Set Work Position to store this position
- If necessary, move the focus slightly up to remove the Lower Z limit reached message displayed on the touchscreen
- Press Home>Microscope>Control>Objectives>2.5x to select the 2.5x objective
- If asked, tap Done to remove the oil lens cleaning warning
- Press Home>Microscope>XYZ>Position>Z-Position>Set zero>Auto to perform focus calibration
- Press OK to start the focus calibration procedure
- Wait a few seconds for the calibration to be completed
| Note |
|---|
Once calibrated, the focus can be found at Z = 1.1 mm). The Z value can be found on the microscope touch screen Home>Z-Position |
|
| UI Expand |
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| | Warning |
|---|
| Make sure to calibrate the focus before performing the first focus. |
On the microscope touch screen: - Press Home>Microscope>Turret>Objectives
- Press 2.5x to select the 2.5x lens
| Info |
|---|
The 2.5x objective is the safest because it has the longest working distance (9 mm). The sample will appear perfectly sharp long before the lens approaches it. It is recommended to always first focus with the safest lens. The objectives are para-focal, focusing with the safest objective will then allow you to easily find your sample with another objective. |
Press Home>Load Position to lower the objectives to its lowest positionPress Set Work Position to store this position If necessary, move slightly adjust the focus slightly up upward to remove clear the Lower Z limit reachedLimit Reached message displayed on the touchscreentouch screen - Place the test slide on the microscope stage with the coverslip
toward - facing the objective
Always use the to perform the first focuswill significantly reduce the time required to set up the instrument. |
- If necessary,
move - adjust the stage
so - to ensure that the sample is
centered on - centred under the objective
On the computer: Open ZenIn Zen: - In
the - the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP,
Rhodamine- Cy3,
etc…- Cy5) to activate the configuration
- Adjust the focus with the main dial while looking through the eyepieces until the image is perfectly sharp
note
| Info |
|---|
Once calibrated, the focus | can be 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
1mm). The Z value can be found on the microscope touch screen Home>Z-PositionIn the Locate - tab, select Off to turn off the illumination
|
| UI Expand |
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| title | Secondary Seconday focus |
|---|
| | Warning |
|---|
| First focus with Perform the initial focus using the safest lens before selecting another lens and continuing with secondary focusobjective before switching to higher-magnification objectives. |
| UI Expand |
|---|
| title | Focusing with air objectives |
|---|
| After performing the first initial focus, on the microscope touch screen: - Press Home>Microscope>Control>Objectives
- Press 10x, 20x or , 40x or 63x (0.75) to select the desired lensobjective
he T| The 40x objective is the best Air objective because it has the largest | numerical Numerical aperture (0.75) together with a wider field of view (40x).
|
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
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! |
| UI Expand |
|---|
| title | Focusing with oil lensesobjectives |
|---|
| After performing the first initial focus, on the microscope touch screen:
- Press
Home>Microscope>Control>- Home>Microscope>Turret>Objectives
Press 63x Oil (1.4)to select the desired objective.The microscope will automatically lower the objective stage so that the sample is becomes accessible.
- Place a single drop of oil on
your sample- the objective
- Press Done. The microscope will automatically return the
sample - objective to its original position
In Zen : - In
the - the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP,
Rhodamine- Cy3, DsRed,
etc…- Cy5) to activate the configuration
- Adjust the focus with the precision dial while looking through the eyepieces
until the - until the image is perfectly sharp
- In the Locate tab,
select - select Off to turn off the illumination
off
Your sample is ready for acquisition! |
|
|
| UI Expand |
|---|
| - Files can be saved 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).
| Note |
|---|
In any case, your files should be removed from the C: drive. |
|
| UI Expand |
|---|
| - 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 strip (#2A) and close the CO2 cylinder (#2B) Select the 2.5x objective and press load position to bring the objectives to the bottom position
Turn off the microscope power bar (#3) Turn off the microscope power bar (#3) - Turn Turn off the computer
- Cover the instrument with the protective dust cover
| Note |
|---|
| title | Important RemindersReminder |
|---|
| - 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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| idtitle | LightpathLog |
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| title | Lightpath |
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| The following schematics depict the light path for transmitted (bright-field and Phase Contrast) and reflected (fluorescence) lights. | View file |
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| name | Zeiss_Z1-Colibri_LightPath.pdf |
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| height | 250 |
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| Tabs Page |
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| Available manuals |
| Tabs Page |
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| Log| UI Expand |
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| - Measure Power output
- Modify camera power supply cable
|
| UI Expand |
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| title | 2025-10-22 Windows 11 and more |
|---|
| - Installation of Windows 11
- Added CO2 connection to incubation module
- Cable management
- Replaced video card
|
| UI Expand |
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| title | 2025-09-01 Camera upgrade |
|---|
| - Added compressed air connexion to the anti-vibration table
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| | UI Expand |
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| title | 20242025-09-01 Camera upgrade |
|---|
| - AxioCam replacement with PCO Edge 5.5
|
| UI Expand |
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| title | 2025-08-21 Wiki Updated |
|---|
| - Updated wiki with complete specifications
|
| UI Expand |
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| title | 2024-02-22 Microscope Firmware 02-22 Microscope Firmware update |
|---|
| - Microscope Firmware update to add Colibri to the touchscreen
- Zen 3.5 HotFix 10
|
| UI Expand |
|---|
| - Computer replacement
- Added Colibri
- Added startup procedure
- Parafocality and paracentrality
|
| UI Expand |
|---|
| - Added complete description
|
|
| Tabs Page |
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| idtitle | Technical Datasheet | title |
|---|
| 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 Sensotech, Part number 432903-9011-000, #14 07 132052; Scan IM 130x100-2mm 90-24-550-0000 Serial 16053038
Stage Controller 90-76-200-0820-024-1803 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
- 6Multi-well plate
- 35 mm dish
- Multi-well plat
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 MR R3 MRm Model: r3.1 Part Number: 426509-9901-000. Serial: 1 22 12 5537
Workstation- PCO Edge 5.5 Model pco.API.Air.BX Serial 6000001404
Workstation- ComputerFujitsu Esprimo
- Intel Core i5-4670 @ 3.4 GHz
- RAM 32 GB DDR3 1600 MHz ECC (4 x 8 GB)
- 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 DriveOS 500 GB
- Storage2 TB HD Data Storage (2 x 1 TB spanned volume)
- Video Card AMD Card DDR5 dedicated memory
- DDR5 0.768 TFLOPS 1x PCIe gen2 x16
- Monitor
- LG Flatron E2711 27' 1920 x 1080
- LG W2442 1920 x1080
- Software SN=
- Serial 1121159628-524292
- HASP
=1798977001
- 1798977001
- Extended Focus
- Measurements
- Multi-Channel
- Panorama
- Software autofocus
- Time Series
- Z-stack
Incubation- Pecon stage top incubation
ConsumablesAnti-vibration table- TMC Model 63 512 Serial 933240
- Plain table top
Consumables- CO
- CO2 Tank
- N2 Tank
- Oil
- Lens Cleaner
Manuals |
| Tabs Page |
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| Tabs Page |
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id | FAQ |
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| title | Troubleshooting & FAQ |
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| Troubleshooting| UI Expand |
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| title | I see a high background in fluorescencedon'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
The fluoresncece light source is a Colibri while the transmitted light is a LED. What happens is that the fluorescence illumination reflects and into the LED and give a high background. To solve this: - Tilt the transmitted light arm backward
or Stop the light from entering the transmitted LED by using a cardboard
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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
Image AddedZ Stack animation Image AddedMaximum Intensity projection of a Z-Stack Image AddedExtended Depth of Focus projection of a Z-Stack
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