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titleFrançais
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urlhttps://wiki.umontreal.ca/display/Microscopie/Zeiss +Axio-Observer+Z1

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idInstrument Tabs
titleZeiss Axio-Observer Z1
directionhorizontal
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idDescription
titleDescription

Zeiss Axio-Observer Z1 inverted microscope

Roger Gaudry Building, Room R-421

Z1 Colibri


Zeiss Z1-Colibri Microscope

Desmarais Building, Room 2234
Simple Microscope usage price
Instrument awarded to Dr. Audrey Claing and Dr. Jean-Philippe Gratton by the Canadian Foundation for Innovation (CFI) in 2014


 

Applications

  • Inverted microscope
  • Widefield imaging
    • Brightfield

Bright-field
    • Phase contrast
    • Fluorescence
  • Incubation
  • Timelapse imaging
  • Deconvolution
  • Extended Depth of Focus

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idDescription
titleDescription

Description

Light sources

  • LED lamp for transmitted light

  • Colibri 7
(385
  • R[G/Y]B-UV (385/469/555-590/631) for fluorescence
Expand
title
Full specifications of the Zeiss Colibri 7 light source
Complete specifications

Emission peak (nm)

Nominal Power (mW)Measured Power (mW)
385/30150 
469/38110 
555/3031
32Information
 
631/33
52
50 

View file
nameZeiss_Colibri-7_Product Information.pdf
height250

Image Added

Objectives

20x10x/0.25 Air Ph1 WD 6.5
  1. 2.5x/0.

5 Air Ph2 WD 2.0
  • Empty
  • 63x/1.4 Oil DIC WD

  • Empty
  • 2.5x/0.075 Air WD 2.0
    1. 075 Air

    2. 10x/0.25 Air Ph1
    3. 20x/0.5 Air Ph2
    4. 40x/0.75 Air Ph2

    5. 63x/0.75 Air Ph2 Long Distance
    6. 63x/1.4 Oil

    Expand
    title
    Objectives complete
    Complete specifications
    PositionNameBrandFull nameIDMagnificationNumerical ApertureImmersionTypeWorking distance (mm)Transmittance
    (% [nm])
    TechniqueCover glass thickness (mm)
    1
    20x
    2.5x/0.
    5
    075 AirZeiss
    20x
    2.5x/0.
    50 Ph2420351
    075
    EC Plan-Neofluar
    M27991020x
    2.5x0.075AirPlan
    -
    Neofluar
    2
    9.
    0800, PhC
    , Fluo0.17
    2

    Empty

    363x/1.4
    10x/0.25 AirZeiss
    63x
    10x/
    1
    0.
    25 Ph1
    Plan
    N-
    Apochromat Oil
    M27
    Achroplan420941-9911
    420782-990063x
    10x
    1
    0.
    4
    25
    Oil
    Air
    Plan Apo
    N-
    chromat
    AchroPlan
    0

    6.

    19>80% [450-750]

    5

    Not AvailableBF, PhC, Fluo0.17
    4Empty5
    320x
    2.5x
    /0.
    075
    5 AirZeiss
    2.5x
    20x/0.
    075420320-9901
    50 Ph2
    EC Plan-Neofluar
    M27 2.5x
    20x0.
    075
    50AirPlan
    -
    Neofluar
    9
    2.
    5>90% [400-750]
    0Not AvailableBF, PhC, Fluo0.17
    6
    4
    10x

    40x/0.

    25

    75 Air

    Zeiss
    10x
    40x/0.
    25 Ph1
    N-Achroplan
    M27 
    75 Ph2
    EC Plan-Neofluar

    420361-9910

    420941-991110x

    40x

    0.
    25
    75

    Air

    AchroPlan
    Plan Neofluar
    6
    0.
    5>80% [400-800]
    71Not AvailableBF, PhC, Fluo

    0.17

    Filter cubes
  • DAPI
  • GFP
  • DsRed
  • DHE (dihydroethidium)
  • Cy5
  • Quadruple DAPI/GFP/Cy3/Cy5
    Expand
    titleFilters complete specifications
    PositionNameBrandIDExcitation filterDichroic mirrorEmission filterComments1DAPI
    Filter Set 49Zeiss

    488049-9901

    365/50
    [325-375]395LP445/50
    [420-470]2GFP
    Filter Set 13Zeiss488013-0000

    470/20
    [460-480]

    495LP

    517/25
    [505-530]3DsRed
    Filter Set 43Zeiss

    000000-1114-101

    545/25
    [533-567]570LP605/70
    [570-640]4DHECustom

    Custom

    500/50
    [475-525]

    540LP580/20
    [570-590]Undefined specifications
    Best guess values5Cy5
    Filter Set 50Zeiss488050-9901640/30
    [625-655]660LP

    690/50
    [665-715]

    6Quadruple
    DAPI/GFP/Cy3/Cy5
    FS90 HE LED
    489090-9110-000
    QBS 405 + 493 + 575 + 653

    QBP 425/30+514/30+592/25+709/100

    Excitation filters included in the light source FS90 HE LED
    • Detector
      • Zeiss AxioCam MR R3 CCD Camera 1388 x 1040 pixels, 12-bit, 13 images/s at full resolution, detector size 8.9 mm x 6.7 mm
    Tabs Page
    idUser Guide
    titleUser Guide
    UI Expand
    expandedtrue
    titleStartup
    1. Remove the dust cover from the microscope

    2. Turn on the computer (#1)

    3. If necessary, turn on the power bar for the incubation module (#2A) and open the CO2 cylinder (#2B)
    4. Turn on the power bar at the left of the computer monitor (#3)

    5. Press the microscope start button located on the rear left of the microscope (#4)

    6. Log in Windows using your UdM credentials
      Note

      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.

    7. Start the Zen software
    UI Expand
    titleFirst Use
    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.
    563x/0.75 Air
    Zeiss

    63x/0.75 Corr Ph2
    LD Plan-Neofluar

    421381-9970-000

    63x

    0.75

    AirLD Plan-Neofluar1.7 at cover glass 0.75Not AvailableBF, PhC, Fluo

    0 - 1.5

    663x/1.4 OilZeiss63x/1.4 DIC
     Plan-Apochromat Oil
    420782-9900-00063x1.4OilPlan Apochromat0.19>80% [400-700]BF, Fluo0.17

    Filter

    1. DAPI
    2. GFP
    3. Rhodamine
    4. DHE (dihydroethidium)
    5. Cy5
    6. Quadruple DAPI/GFP/Cy3/Cy5
    Expand
    titleComplete specifications
    PositionNameBrandIDExcitation filterDichroic mirrorEmission filterComments
    1DAPI
    Filter Set 49
    Zeiss

    488049-9901

    365/50
    [325-375]
    395LP445/50
    [420-470]

    2GFP
    Filter Set 13
    Zeiss488013-0000

    470/20
    [460-480]

    495LP

    517/25
    [505-530]

    3DsRed
    Filter Set 43
    Zeiss

    000000-1114-101

    545/25
    [533-567]
    570LP605/70
    [570-640]

    4DHECustom

    Custom

    500/50
    [475-525]

    540LP580/20
    [570-590]
    Undefined specifications
    Best guess values
    5Cy5
    Filter Set 50
    Zeiss488050-9901640/30
    [625-655]
    660LP

    690/50
    [665-715]


    6Quadruple
    DAPI/GFP/Cy3/Cy5
    FS90 HE LED
    Zeiss489090-9110-000


    QBS
    405+493+575+653

    QBP 425/30+514/30+592/25+709/100

    Excitation filters included in the light source FS90 HE LED

    Detectors

    • PCO Edge 5.5
      Expand
      titleComplete specifications
      CameraPCO 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 resolution100 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

      View file
      namePCO_Edge 5.5_Datasheet.pdf
      height250

    • Zeiss Axiocam MRm (not installed)
    Expand
    titleComplete specifications
    CameraZeiss Axiocam MRm

    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 resolution13 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
    nameZeiss_AxioCam MRm_Datasheet.pdf
    height250

    Tabs Page
    idUser Guide
    titleUser Guide

    User Guide

    UI Expand
    expandedtrue
    titleStartup
    1. If not already done, turn on the computer (#1) and log in to Windows using your UdeM credentials
    2. Remove the dust cover from the microscope
    3. 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

      Make sure the humidifier is properly filled with distilled water.

    4. Turn on the microscope power bar (#3) on the desk near the computer

    5. 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.
    6. Start Zen
    UI Expand
    titleFirst Use

    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).

    1. If Zen is open, close it and wait until it has completely shut down (this may take up to 30 seconds)

    2. On the Desktop, open the Softwares folder

    3. Double-click Zen Settings for Zeiss Z1-Colibri

    4. A script will run and a black window will appear briefly

    5. When the message Settings for Zen have been imported successfully appears, click OK to close it

    6. You can now open Zen

    UI Expand
    titleLoading samples

    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
    titleCalibration

    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

    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
    titleThe calibration dialog did not appear...

    The system may already be calibrated. This can occur if a previous user calibrated the system and left it on.

    UI Expand
    titleVerifying if the system is already calibrated

    In Zen, within the Focus tab, located on the right side of the screen:

    1. Click Load to lower the objective

    2. The Z position is indicated below Current
    3. If Z position value is less than 100 um the system is calibrated

    On the microscope touch screen:

    1. Lower the objective by pressing Home > Load Position

    2. Press Set Work Position to store this position

    3. If necessary, slightly adjust the focus upward to clear the Lower Z Limit Reached message displayed on the touch screen

    4. The Z position value is indicated
    5. If the value is less than 0.1 mm then the system is calibrated
    UI Expand
    titleManual calibration with the software

    In Zen, within the Stage tab, located on the right side of the screen:

    1. If not already done, check the Show All option
    2. At the bottom of the tab click Calibrate

    3. A warning message will show up click Continue

    4. 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:

    1. If not already done, check the Show All option
    2. At the bottom of the tab click Calibrate

    3. A warning message will show up click Continue

    4. The microscope will then perform a Z calibration and then return to its original position

    XY and Z calibrations are now complete

    UI Expand
    titleManual calibration with the microscope touch screen

    On the microscope touch screen:

    1. Navigate to Home > Microscope > XYZ > Position > Z-Position > Set Zero > Auto to perform focus calibration

    2. Press OK to start the calibration procedure

    3. Wait a few seconds for the calibration to complete

    4. Lower the objective by pressing Home > Load Position

    Note

    Please note, this procedure will delete all your experiment protocols and restore the software to its original settings.

    1. If open, close the Zen software and wait for it to close completely (up to 30 seconds)
    2. On the Desktop open the Documentation folder
    3. Double-click Settings for Axio-Osberver Z1
    4. A script will run and a black window will appear briefly
    5. You can then reopen the Zen software
    UI Expand
    titleLoading samples

    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
    titleFocus Calibration Z

    On the microscope touch screen:

    Press Home>Load Position to lower the stage to its lowest position
    1. Press Set Work Position to store this position

    2. If necessary,

    move
    1. slightly adjust the focus

    slightly up
    1. upward to

    remove
    1. clear the

    “Lower
    1. Lower Z

    limit reached”
    1. Limit Reached message displayed on the

    touchscreen
    1. touch screen

    2. Navigate to Home > Microscope > XYZ > Position > XY-Position > Set Zero > Auto to perform a stage

  • Press Home>Microscope>Turret>Objectives>10x to select the 10x 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
    1. calibration

    2. Press OK to start the

    focus
    1. calibration procedure

    2. Wait a few seconds for

    the calibration to be completed NoteOnce calibrated, the focus can be found at Z = 1.5 mm). The Z value can be found on the microscope touch screen Home>Z-Position
    1. the calibration to complete

    XY and Z calibrations are now complete

    UI Expand
    titleEnsuring the calibration dialog is displayed at startup

    In Zen:

    1. In the menu bar, navigate to Tools > Options

    2. Select Startup/Shutdown

    3. Under Stage/Focus Calibration, ensure Request Stage/Focus Calibration on Startup is checked

    4. Click OK to close the Options dialog

    UI Expand
    title
    First
    Initial focus
    Warning
    titleImportant
    Make sure to calibrate the focus before performing the first focusPress 10x to select the 10x lens
    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:

  • Press Home>Microscope>Turret>Objectives
    1. If not already done, select the lowest-magnification objective Home > Microscope > Control > Objectives > 2.5x
    Info

    The

    10x objective is the safest because it has the longest

    2.5× and 10× objectives are the safest to use due to their long working distance (

    6.5

    >6 mm). The sample will appear

    perfectly

    in sharp

    long

    focus well before the

    lens

    objective approaches it. It is recommended

    to always first

    to always focus

    with

    using the safest

    lens

    objectives first.

    The

    Since the objectives are

    para-focal

    parafocal, focusing with the safest

    objective will then allow you to easily find your sample with another objective.

    objectives will facilitate locating the sample when switching to higher-magnification objectives.

    1. Lower the objective by pressing Home > Load Position

    Press Home>Load Position to lower the stage to its lowest position
    1. Press Set Work Position to store this position

    2. If necessary,

    move
    1. slightly adjust the focus

    slightly up
    1. upward to

    remove
    1. clear the

    “Lower
    1. Lower Z

    limit reached”
    1. Limit Reached message displayed on the

    touchscreen
    1. touch screen

    2. Place the test slide on the microscope stage with the coverslip
    toward
    1. facing the objective
      Note
      titleImportant
    Always use the
    1. Using a test slide

    to perform the first focus
    1. will significantly reduce the time required to set up the instrument.

    2. If necessary,
    move
    1. adjust the stage
    so
    1. to ensure that the sample is
    centered on Open the Zen software
    1. centred under the objective

    On the computer:

    In Zen:

    1. In
    the
    1. the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP,
    DsRed
    1. Cy3,
    DAPI, etc…
    1. Cy5) to activate the configuration
    2. 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 =

      1.5mm). The Z value can be found

    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

    Home>Z-Position

    under Home > Z-Position, as well as in Zen within the Focus tab, located on the right side of the screen.

    1. In the Locate tab, select Off to turn off the illumination
    UI Expand
    titleSeconday focus
    Warning
    titleImportant
    First

    Perform the initial focus

    with

    using the safest

    lens before selecting another lens and continuing with secondary focus

    objective before switching to higher-magnification objectives.

    UI Expand
    titleFocusing with air objectives

    After performing the

    first

    initial focus, on the microscope touch screen:

    1. Press
    Home>Microscope>Turret>
    1. Home>Microscope>Control>Objectives
    2. Press 10x, 20x
    or 40x
    1. 40x or 63x (0.75) to select the desired
    lens
    1. 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).
    largest Numerical aperture (0.75) together with a wider field of view (40x).

    In Zen:

    1. In the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP, Cy3, DsRed, Cy5) to activate the configuration
    It offers a lateral resolution of 420nm at a wavelength of 550nm.
    1. Adjust the focus with the precision dial while looking through the eyepieces until the image is perfectly sharp
    2. In the Locate tab, select Off to turn off the illumination

    Your sample is ready for acquisition!

    UI Expand
    titleFocusing with oil
    lensesThis microscope does not have oil immersion
    objectives
    . However, if there were, the procedure would be as follows:

    After performing the

    first

    initial focus, on the microscope touch screen:

    1. Press Home>Microscope>Turret>Objectives

    Press 63x Oil, 100x Oil (1.3) ou 100x Oil (1.4) to select the desired lens. The microscope will automatically lower the stage so that the sample is accessible.

    InfoThe 63x objective is the best oil objective because it has the most optical corrections (Plan Apochromat) and the largest numerical aperture
    1. Press 63x Oil (1.4)

    .
    It offers a lateral resolution of 240nm at a wavelength of 550nm
    1. to select the desired objective. The microscope will automatically lower the stage so that the sample becomes accessible.

    2. Place a single drop of oil on
    your sample
    1. the objective
    2. Press Done. The microscope will automatically return the
    sample
    1. objective to its original position

    In Zen

    Blue software

    :

    1. In
    the
    1. the Locate tab, select BF or the desired fluorescence (Fluo, DAPI, GFP, Cy3, DsRed,
    DAPI, etc…
    1. Cy5) to activate the configuration
    2. Adjust the focus with the precision dial while looking through the eyepieces until the
    eyepieces until the
    1. image is perfectly sharp
    2. In the Locate tab,
    select
    1. select Off to turn off the illumination
    off

    Your sample is ready for acquisition!

    UI Expand
    titleStorage management
    • 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
    titleShutdown
    1. Save your data
    Close the Zen software
    1. Close Zen
    2. Transfer your data to the D: drive (Data Storage) or to your external drive and delete it from the local C: drive
    3. If used, clean oil objectives with lens cleaner and paper
    4. Select the lowest magnification objective and press load position to place the objectives in a safe position
    5. If used, turn off the incubation module power

    strip Select the 10x objective and press load position to bring the objectives to the bottom position
    1. strip (#2A) and close the CO2 cylinder

    (#2B)
    1. (#2B)

    2. Turn off the microscope power bar (#3)

    3. Turn off the computer
    4. Cover the instrument with the protective dust cover
    Note
    title
    Important Reminders
    Reminder
    • Take back your samples including ones in the microscope
    • Leave the microscope and the working area clean

    Tabs Page
    id
    title
    Lightpath
    Log
    titleLightpath

    The following schematics depict the light path for transmitted (bright-field and Phase Contrast) and reflected (fluorescence) lights.

    PDF
    nameLightPath_Zeiss_Z1.pdf

    Log

    UI Expand
    titleTo be done
    • Measure Power output
    • Modify camera power supply cable
    UI Expand
    title2025-10-22 Windows 11 and more
    • Installation of Windows 11
    • Added CO2 connection to incubation module
    • Cable management
    • Replaced video card
    UI Expand
    title2025-09-01 Camera upgrade
    • Added compressed air connexion to the anti-vibration table
    UI Expand
    title2025-09-01 Camera upgrade
    • AxioCam replacement with PCO Edge 5.5
    Tabs Page
    idManuals
    titleManuals

    Available manuals

    Tabs PageidLogtitleLog
    UI Expand
    title
    To do
    • Check stage tilt
    • Ask for Colibri Remote
    • Ask for fluorescence backlight from LED
    2025-08-21 Wiki Updated
    • Updated wiki with complete specifications
    UI Expand
    title2024-02-22 Microscope Firmware update
    • Microscope Firmware update to add Colibri to the touchscreen
    • Zen 3.5 HotFix 10
    UI Expand
    title2022-05-09
    • Computer replacement
    • Added Colibri
    • Added startup procedure
    • Parafocality and paracentrality
    UI Expand
    title2022-03-17
    • Added complete description
    UI Expand
    title2021-09-27
    • Added to wiki
    Tabs Page
    id
    titleTechnical Datasheet
    title

    Technical Datasheet

    Stand

    • Zeiss Axio-Observer Z1
    inverted 
    • inverted Serial: 3851001242 Part Number: 431007-9902-000
      System ID: 1024979772
    • Camera adapter Model 60N-C, 1", 1x, Model: 426114

    Light sources

    • Transmitted LED light
    • Colibri 7 R(G/Y)B-UV 423052-9730-000 Serial 5440000661

    Condenser

    • Manual
    condenser Product number: TBD, Serial: TBDEmpty
    • condenser
    • Lens NA 0.35 WD 70 mm Part Number: 424241

    • Filter turret 6 positions manual

      1. H

      2. Ph0
      3. Ph1

      4. Ph2

      5. DIC

      6. DUC

    Objectives

    1. 2.5x/0.

    085 Air WD 8.8
    1. 075 Air 420320-9901-000

    Empty

    1. 10x/0.25 Air Ph1

    WD 6.5
    1. 420941-9911-000


    1. 20x/0.5 Air Ph2

    WD 2.0
    1. 420351-9910-000

    2. 40x/0.75 Air Ph2 420361-9910-000

    3. 63x

    40x
    1. /0.

    95 Air WD 0.25

    Stage

    • Motorized stage Marzhauser Sensotech, Part number 432903-9011-000, #14 07 132052; 90-76-200-0820
    • Remote control joystick
    • Inserts
      • Slide combo
      • 6-well plate
      • 35 mm dish
      • Multi-well plat

    Filters

    1. DAPI Filter Set 49
    2. GFP Filter Set 13
    3. Rhodamine Filter Set 43
    4. DHE (dihydroethidium) 424931
    5. Cy5 Filter Set 50
    6. Multiband FS90 HE LED

    Detector

    • Zeiss AxioCam MR R3 CCD Camera 1388 x 1040 pixels, 12-bit, 13 images/s at full resolution, detector size 8.9 mm x 6.7 mm. Model: r3.1 Part Number: 426509-9901-000. Serial: 1 22 12 5537

    Workstation

    Fujitsu Esprimo P920 E90+
    1. 75 Air Ph2 Long Distance 421381-9970-000

    2. 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

    1. DAPI Filter Set 49 488049-9901
    2. GFP Filter Set 13 488013-0000
    3. Rhodamine Filter Set 43 000000-1114-101
    4. DHE (dihydroethidium) 424931
    5. Cy5 Filter Set 50 488050-9901
    6. 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
    32 GB DDR3 1600 MHz ECC (4
      • 24 GB DDR3 800 MHz (3 x 8 GB)
    • OS
    500 GB
    • Drive
      • 1 TB SSD 550 MB/s
      • Win 11 23H2
    • Storage
      • 2 TB HD
    Data Storage (2 x 1 TB spanned volume) Monitor
      • 110 MB/s
    • Video
    Card AMD FirePro V4900 1 GB DDR5 dedicated memory
    • 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
      YRMDZ 1798977001 1798977001

      Incubation

        • 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
      Pecon stage top incubationN

      Consumables

      • CO
      2 Tank
      idFAQ
      titleTroubleshooting & FAQ
      titleTroubleshooting & FAQ

      Troubleshooting

      UI Expand
      titleI don't see any fluorescence!

      Technical support is free and unlimited. Contact us !

      Troubleshooting

      UI Expand
      titleI see a high background in fluorescence
      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

      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
      or
      • Close the manual shutter between the condenser and the transmitted light
      • Use a higher magnification objective
      Stop the light from entering the transmitted LED by using a cardboard

      FAQ

      UI Expand
      titleCan I use this microscope to look at cell in a dish?

      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.

      UI Expand
      titleCan I use this microscope to perform timelapse experiments?

      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.

      UI Expand
      titleWhat is Extended Depth of Focus?

      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 animationImage AddedMaximum Intensity projection of a Z-StackImage AddedExtended Depth of Focus projection of a Z-StackImage Added

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      titleZeiss Axio-Observer Z1
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      titleDemo Image
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