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Nikon Eclipse E-600 upright microscope

Roger Gaudry N-620

  • Applications
    • Brightfield
    • Phase Contrast
    • Polarized light
    • Fluorescence
  • Light sources

    • Halogen lamp for transmitted light

    • Mercury lamp (350~600nm) for fluorescence 

  • Objectives:

    • 10x/0.3 Air Ph1

    • 40x/0.75 Air Ph2

    • 100x/1.3 Oil Ph3 WD 0.2

PositionNameBrandMagnificationNumerical ApertureImmersionTypeWorking distance (mm)Transmission curveTechnique
110x/0.3 AirNikon10x0.3AirPlan Fluor1610x/0.3 Air Plan Fluor Ph1 DLLBF, Pol, PhC, Fluo
2

40x/0.75 Air

Nikon40x

0.75

Air

Plan Fluor0.7240x/0.75 Air Plan Fluor Ph2 DLLBF, Pol, PhC, Fluo
3100x/1.3

Oil

Nikon

100x

1.3OilPlan Fluor0.2 100x/1.3 Oil Plan Fluor Ph3 DLLBF, Pol, PhC, Fluo
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  • Filter cubes

    • DAPI/Hoechst/AMCA
    • FITC/EGFP
    • TRITC/Rhodamine

    • TxRed

PositionCube nameBrandIDExcitation FilterDichroic mirrorEmission Filter
1DAPI/Hoechst/AMCAChromaCube set 31000v2350/50x [325-375]400LP460/50m [435-485]
2FITC/EGFPChromaCube set 41001

480/40x [420-500]

505LP

535/50m [510-560]
3TRITC/RhodamineChroma

Cube set 41002c

545/30x [530-560]570LP620/60m [590-650]
4Texas RedChroma

Cube set 41004

560/55x [532-588]

595LP645/75m [607-682]
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  • Detector
    • Color CMOS Nikon DS-Ri2 4908 x 3264 pixels,14-bit, 6fps at full frame


Startup

Turn on the computer

Turn on the microscope power bar

If fluorescence is required, turn on the mercury lamp power supply unit (3A) and press ignition (3B)

Mercury lamp must be on for at least 30 min before being turned off and vice-versa

Log in Windows using your UdM credentials

Start-up NIS-Elements

The first time you log in the computer, you need to import the microscope settings. To do this follow the instructions Nikon Eclipse E600-en


Shutdown

Save your data

Close NIS-Elements

Transfer your data to the D: drive (Data Storage) or to your external drive and delete it from the local C: drive

Get your samples from the microscope

If used, clean the oil objective with lens cleaner and lens paper

If fluorescence was used, turn off the mercury lamp power supply unit (3A)

Turn off the microscope power bar (2)

Wait until the lamps are cool and cover the microscope


Important Reminders

Take back your samples including ones in the microscope

Leave the microscope and the working area clean

Mercury lamp must be on for at least 30 min before being turned off and vice-versa


Storage Management

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).

In any case, your files should be removed from the C: drive.


Setting-up NIS-Elements

This is required the first time you are using the instrument. You will usually do it during the training session. It can be performed if something is not working properly right or if you want to refresh the software interface.

This process will delete all experiment protocols and restore the parameters for the microscope

Close NIS-Elements

Wait until the complete closure of NIS-Elements

Open the folder Desktop\Logiciels

Open the software NIS Settings Utility

Click on the Import tab

Click on Browse

Navigate to your desktop

Select the file Nikon-E600 Settings.bin

Click Select

Select all items

Click Import

Click OK

Close the NIS Settings

Follow the schematics below for Transmitted light (Bright field, Phase Contrast, Polarized light) and transmitted light (fluorescence).

To do

Adjust focus drive jitter

Add a holder for polarized light analyzer


2021-07-20

Replacement mercury lamp bulb HBO 1003W/2

256 GB SSD added in workstation for OS

Windows 10 Installation

BIOS updated to v2.47

Camera Firmware updated to v2.11

NIS-Elements Basic Research v4.6 64-bits installed

Creation NIS Elements Settings

FITC and TxRed cubes excitation and emission filters slightly damaged. Dichroic OK


2018-04-04

Nikon Preventive Maintenance

Adjustment and cleaning Stage Nosepiece, condenser, filter turret, focus drive, shutters

100x slightly damaged but not the lens

Fluorescence cubes damaged: FITC TxRed

Focus drive has a jutter

Stand

Nikon Eclipse E600 upright Serial 725540


Light sources

Transmitted light Halogen 12V 100W Serial 01875599

Reflected light

Power supply Nikon Mercury lamp Type C SHG1 Serial D12139

Bulb housing model LH M100C-1 Serial 039326


Condenser

Condenser Universal C-CU Serial 081901

Lens Dry NA 0.9

Filters: Empty, Ph1, Ph2, Ph3, DICM, DICH, Empty


Objectives

1

40x/0.75 Plan Fluor Ph2 DLL WD 0.72 Air (Transmission curve) with PF40 Wollaston prism

100x/1.3 Plan Fluor Ph3 DLL WD 0.2 Oil (Transmission curve) with PF/PA 100 Oil Wollaston prism

Empty

Empty

Empty


Turret

PositionCube nameBrandIDExcitation FilterDichroic mirrorEmission Filter
1DAPI/Hoechst/AMCAChromaCube set 31000v2350/50x400LP460/50m
2FITC/EGFPChromaCube set 41001

480/40x

505LP

535/50m
3TRITC/RhodamineChroma

Cube set 41002c

545/30x570LP620/60m
4Texas RedChroma

Cube set 41004

560/55x

595LP645/75m
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Detector

Camera Nikon DS-Ri2 Serial 701234


Workstation

HP Z440 Workstation

Intel Xeon E5-1630 v3 @ 3.7GHz

RAM 32 GB DDR4 2133 MHz  (4 x 8 GB)

OS 256GB SSD 550 MBs

2TB HD Data Storage 150 MBs

Video Card NVIDIA Quadro K620 2 GB DDR3 dedicated memory

Monitor HP Z24i display 24' 1920x1200


Consumables

Mercury lamp bulb OSRAM HBO 1003W/2 100W

Tungsten Halogen Lamp OSRAM 64623 HLX 100W 12V 

Nikon Eclipse E600 Microscope

Cells courtesy of Benoit Bessette and Monique Vasseur (Biochemistry)

Images courtesy of Dr Shirley Campbell and Emilie Fiola-Masson (Pharmacology)

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