Michael Hooker Microscopy Facility (MHMF.ORG)

Leica DMIRB Inverted Microscope with Color & B/W Cooled Digital Cameras

Location: 6129 Thurston Bowles

Notices

• If you are the last user of the day, especially later in the day, please turn off the mercury arc lamp when you a re finished.
• Please do not start mercury arc lamp if lamp housing is warm.  It must be cool!  (In order to avoid damage or explosion mercury arc lamps must cool for ~30 minutes before being restarted.)
• If you plan to use this microscope for more than ~30 minutes at a time please book ahead at the Leica Inverted microscope booking page.
• Due to occasional high demand, all walk up users should check the booking page to ensure the machine is free.
• Camera ports:
  • The left side port transmits 100% of the light with a magnification of 0.63x to a B/W high sensitivity Hamamatsu CCD camera. 
  • The top trinocular port transmits 100% or 50% of light to a Q-Imaging MicroPublisher CCD color camera and has a 1x magnification.
• New! Oct 20, 2006: Fluorescence filter cube for far-red emitting fluorophores (e.g. Cy5, Alexa 633)

Contents

• Introduction
• The Equipment
  • The Microscope
  • Cameras:
  • Comparison of the Cameras attached to the Leica Inverted Microscope - which one to use?
  • Computer:
• Setting Up the Microscope
• Image Acquisition
  • Acquiring Images using SimplePCI (Hamamatsu B/W or Q-Imaging Color Camera)
  • Using the Q-Imaging Color Camera with Q-Capture

Introduction

The Leica microscope is a standard inverted microscope set up for transmitted light, differential interference contrast (DIC or Nomarski) and fluorescence microscopy.  Images may be viewed by eye or viewed and saved to computer with either of 2 cameras.  For transmitted light and bright fluorescence imaging a chilled color camera is mounted on top of the trinocular and can be used to capture high resolution digital images.  For dimly fluorescent samples or photometric quantification, a chilled B/W CCD camera (an OrcaER) made by Hamamatsu is attached to the side port on the left of the microscope.  DIC images may also be captured using either camera, although the color camera can capture with higher resolution.  The specific hardware attached to this microscopy is listed below.

The Equipment

The Microscope: Leica inverted DMIRB microscope   Objectives:

* These objectives prefer a number 1.5 (170 um) glass cover slip.
** Suitable only for imaging though cover slips due to small working distance
*** When not using DIC, the objective Wollaston should be in the blank (H) position
Use only Leica immersion oil with oil immersion objectives

• Condenser:
  • Type S1    0.9 NA 2 mm working distance (small conical nose lens, screw on/off)
  • Type S23  0.5 NA 23 mm working distance  (large cylindrical nose lens, screw on/off)
  • Type S70   0.? NA 70 mm working distance (remove nose lens)
• Differential Interference Contrast (Nomarski) is available for some of the objectives
• Illumination:
  • Transmitted light - 100 Watt Halogen (Tungsten filament) lamp with neutral density filters and a color temperature correction filter
  • Fluorescence - 100 watt Mercury arc lamp (HBO)
• Dichroic Filters for Fluorescence -
  • Dapi (31000, Chroma)    ex=360/40   di=400lp   em=460/50
  • Texas Red (31004, Chroma)    ex=560/40   di=595lp   em=630/60
  • Fitc (41001, Chroma)    ex=480/40   di=505lp   em=535/50
  • Cy5 (41008, Chroma)    ex=620/60  di=660lp  em=700/75  **NEW Oct 20, 2006**
  • GFP (31019, Chroma)    ex=425/40   di=460lp   em=505/40  (important:- this filter is not suitable for the more common eGFP)
  • eGFP Narrow Band (31026, Chroma)    ex=480/20   di=505lp   em=520/20 (good for minimizing autofluorescence)
  • Triple Dichroic combined Dapi, FITC, Texas Red (61002 Chroma) (note that this filter set can have high cross talk between the fluorescent channels)

   

  • Note 1: The GFP cubes are usually in the plastic tube on the shelf above the microscope table
  • Note 2: The numbered positions of the cubes in the carrousel are sometime changed
  • Fluorescent proteins spectra - Clontech

Cameras:

• Cooled OrcaER  (1.3 mega pixels) or DVC 1312m b/w CCD (1.3 mega pixels) camera
  • Acquisition through C-Imaging only
• Cooled color CCD, MicroPublisher (3.3 mega pixel)     
  • Acquisition either C-Imaging or QCapture software

Comparison of the Cameras attached to the Leica Inverted Microscope

Computer:

• Dell 8200 Tower computer is under the cart
  • Computer name is \\Fresnel   fresnel.med.unc.edu
  • Pentium 4, 2.0 GHz, 512 MByte RAM
  • 24x CD-RW
• Network
  • Name is \\FRESNEL on the MHmicroscopy domain
  • Shared directory on the Windows network is users or users2 and is accessible directly from Windows
    • Can put \\fresnel\users2 in the address box of windows explorer or MyComputer in order to browse the directory.  Enter your facility username as mhmicroscopy\username
    • If you are browsing from Internet Explorer inside UNC try clicking \\fresnel\users2
  • This computer is a member of the MHMICROSCOPY domain
  • The MHMICROSCOPY file server is accessible from this workstations (FRESNEL) computer.  Many users' directories are at  \\minsky\users2.  This shared directory can be mapped to the M: drive on your log in. 
  • Each user requires a username and password on the MHMICROSCOPY domain in order to log on and access the network shares
  • This computer has access to the Xerox Phaser8550dx color printer
• Software:
  • C-Imaging - runs either camera
  • Q-Capture  -  runs cooled CCD color camera only (Micro Publisher, by Q-Imaging)
  • EasyCD Creater 5 (Roxio) - for burning CDs
  • WinZip  -  For compressing files and directories into zip files
  • LViewPro  -  small and quick image viewer for 8 bit b/w and rgb images
  • Photoshop 7
  • ThumbsPlus 7 - for viewing image thumbnails

Parts of the Leica DMIRB microscope

For printing

Setting Up the Microscope

• Powering up
  • If fluorescence is required switch on Mercury Lamp if it is not already on (green switch on external power supply).  Do not turn the lamp on unless the lamp housing is cool.  (Mercury lamps must be have cooled for at least 30 minutes before igniting)
  • Switch on incandescent lamp for transmitted or DIC (switch is on left side in front of lamp voltage wheel (1) )
  • Switch on Hamamatsu camera control box.
  • Switch on computer, if it is not already running.
• Set up optics on the Leica Inverted
  • For transmitted light (Kohler Illumination) - if transmitted not  required then go to fluorescence setup
    • Open field aperture (2)
    • Swing in neutral density filters (3)
    • Minimize condenser aperture (4)
    • Set condenser turret ring to H (brightfield) (5)
    • Lower objectives with coarse focus knob (6)
    • Select no Wollaston prism - "H" position on wheel below objective turret (7)
    • Choose required objective.  (Generally choose a lower power dry objective, locate sample and region of interest and then move to a higher power dry or immersion objective )
    • Pull out analyzer slider on left side of scope (8)
    • Close B/W camera port by pushing in rod on right hand side of microscope (9)
    • Close color camera port by pushing in rod on left side of the trinocular head (10)
    • Set correction collars on eyepieces to just expose silver ring (11).  This makes viewing more comfortable for normal eyes and helps keep parfocality with cameras
    • Ensure incandescent lamp power is at about 10 - check power wheel by rotating away until light can be seen spilling onto condenser (12)
    • Place sample on stage cover slip down - (This is an inverted microscope!)
    • Focus onto sample
    • Close field iris (2) until you see a ring. Focus the image of the ring with the condenser focus knob (5), and center it with the 2 knurled screws at 45 degrees.
    • Open field aperture (2) to just fill the field of view seen through the eye pieces
    • Open condenser aperture (4) to desired contrast.  Remember maximum resolution is obtained with a fully open aperture, which also gives minimum depth of focus & contrast and maximum illumination intensity.
    • These steps have set up Kohler Illumination!
    • Switch to higher power objective if desired
  • For Nomarski (DIC) - if desired
    • Set up for Kohler
    • Open condenser aperture (4) maximally
    • Ensure both Wollaston prisms are not in the light path (5) and (7)
    • Push in analyser
    • Adjust upper polariser for maximum darkness
    • Select condenser Wollaston which matches objective being used (5)
    • Select Wollaston below object (7) which matches objective power used (see table on front of scope body)
    • Adjust Wollaston (7) prism shear for a uniform brick gray kind of color by slightly moving the Wollaston wheel
  • For fluorescence (* denotes steps also described in transmitted light setup)
    • * Lower objectives
    • Pull out analyzer slider on left side of scope (8)
    • Select no Wollaston prism - "H" position on wheel below objective turret (7)
    • * Choose required objective.  (Generally choose a lower power, locate sample and region of interest and then move to a higher power)
    • * Close B/W camera port by pushing in rod on right hand side of microscope
    • * Close color camera port by pushing in rod on right side of microscope and pulling out left side of the trinocular head
    • * Set correction collars on eyepieces to just expose silver ring.  This makes viewing more comfortable for normal eyes and helps keep parfocality with cameras
    • Ensure incandescent lamp is off at the switch on the front left of the scope
    • * Place sample on stage cover slip down - (This is an inverted microscope!)
    • Choose filter set using turret just above the left side camera port
      • 1=none    2=fitc    3=tritc/texas red    4=dapi
    • Open light path from mercury lamp by pulling rod on back left of scope out.  1st position out includes an IR filter (don't use) and all the way out removes the IR filter. 
    • Focus on sample
    • Switch to higher power objective if desired

Image Acquisition

• Images can be acquired with either camera using C-Imaging. 

• For the MicroPublisher camera, the QCapture software may be used instead. 

Acquiring Images Using SimplePCI   <--- please click on this link  

Acquiring Images Using the Q-Imaging Software with the MicroPublisher Color Camera

• Log on the computer
  • enter username (and press tab to move to-)
  • enter password
  • choose domain MHMICROSCOPY (not local computer FRESNEL)
• Choose QCapture    N.B.  clicking on these links should open a view in another window.  This window may be hidden behind other windows on your computer.
  • open control tools  (yellow wrench)
  • open live view  (green play symbol)
  • In the tools window choose bin 1
  • display live image
  • white balance
  • select 8 bit mode, which is generally adequate and makes viewing image file easier
  • auto expose (due to a software bug always do auto expose with a bin of 1, then switch to another bin size as desired)
  • choose resolution (i.e. bin size: 1=2048*1536  2=1024*768  3=768*512  4=512*384)
  • snap image
  • save image
  • repeat ad lib.
• Shutdown
  • Turn off cooler by unchecking box in tools window or unplug Firewire connector to camera
  • Log off
  • Lower objective
  • Clean up oil on all objectives used with immersion oil
  • Power down arc lamp if no one else will be using fluorescence

		Copyright 2001-08  Dr. M. Chua, Office of Research, University of North Carolina, Chapel Hill, NC 27599
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