Specific Process Knowledge/Characterization/Optical microscope: Difference between revisions

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{| border="1" cellspacing="0" cellpadding="6"  
'''Feedback to this page''': '''[mailto:labadviser@nanolab.dtu.dk?Subject=Feed%20back%20from%20page%20http://labadviser.nanolab.dtu.dk/index.php/Specific_Process_Knowledge/Characterization/Optical_microscope click here]'''
!  
 
! Zeiss (RR2)
''This page is written by DTU Nanolab  internal''
! Leica (RR3)
 
! Leitz (RR4 Glassroom1)
[[Category: Equipment|Characterization Optical mi]]
! Zeiss (RR4 Glassroom1)
[[Category: Characterization|Optical mi]]
! Zeiss (RR4)
 
! Nikon (K10 yellow room)
{|border="1" cellspacing="1" cellpadding="3" style="text-align:left;"
|-  
|-
| Magnification
|-style="background:white; color:black; vertical-align:middle; text-align:center;"
|
!Nikon SMZ 1000
!Noco IR
!Leica INM 100
!Zeiss Jenatech
!Nikon Eclipse L200 #1
!Nikon Eclipse L200 #2
!Nikon Eclipse L200N #3
!Nikon Eclipse L200N #4
!Nikon ME 600
!Leica S8 APO
!Zeiss Axiotron
|-
 
|-
|-style="background:white; color:black; vertical-align:middle; text-align:center;"
|
|[[image:Nikon SMZ 1000.jpg|100x100px|thumb|center]]
|[[image:Noco IR microscope.jpg|100x100px|thumb|center]][[image:Noco IR microscope_1.jpg|100x100px|thumb|center]]
|[[image:LeicaINM100.jpg|100x100px|thumb|center]]
|[[image:Zeiss Jenatech strain.jpg|100x100px|thumb|center]][[image:Zeiss Jenatech strain_1.jpg|100x100px|thumb|center]]
|[[image:Nikon Eclipse L200.jpg|100x100px|thumb|center]][[image:Nikon Eclipse L200_1.jpg|100x100px|thumb|center]]
|[[image:Nikon Eclipse L200 2.jpg|100x100px|thumb|center]][[image:Nikon Eclipse L200 2_1.jpg|100x100px|thumb|center]]
|[[image:Nikon Eclipse L 200 3_1.jpg|100x100px|thumb|center]]
|[[image:Nikon Eclipse L 200 4_1.jpg|100x100px|thumb|center]]
|[[image:Nikon ME 600.jpg|100x100px|thumb|center]][[image:Nikon ME 600_1.jpg|100x100px|thumb|center]]
|[[image:Leica S8 APO.jpg|100x100px|thumb|center]]
|[[image:Zeiss Axiotron.jpg|100x100px|thumb|center]][[image:Zeiss Axiotron_1.jpg|100x100px|thumb|center]]
|-
 
|-
|-style="background:LightGrey; color:black; vertical-align:middle; text-align:left;"
!Location
|346-901
|346-901
|346-901
|cleanroom A1
|cleanroom D3
|cleanroom F3
|cleanroom E4
|cleanroom E5
|cleanroom F1
|cleanroom Cx1
|cleanroom D3
|-
 
|-
|-style="background:WhiteSmoke; color:black; vertical-align:middle; text-align:left;"
!Responsible group
|Wet chemistry
|Wet chemistry
|Wet chemistry
|Lithography
|Lithography
|Lithography
|Lithography
|Lithography
|Lithography
|Lithography
|Lithography
|-
 
|-
|-style="background:LightGrey; color:black; vertical-align:middle; text-align:left;"
!Objectives
|Zoom 0.8x - 8x
|
*2.5x
*10x
*20x
*50x
|
*2.5x
*5x
*10x
*20x
*50x
|
*5x
*10x
*20x
*50x
*100x
|
*2.5x
*5x
*10x
*20x
*50x
|
*2.5x
*5x
*10x
*20x
*50x
*100x
|
*2.5x
*5x
*10x
*20x
*50x
*100x
|
*2.5x
*5x
*10x
*20x
*50x
*100x
|
*5x
*10x
*20x
*50x
*100x
|Zoom 1x - 8x
|
*5x
*10x
*20x
*50x
|-
 
|-
|-style="background:WhiteSmoke; color:black; vertical-align:middle; text-align:left;"
!Ocular
|10x
|10x
|10x
|10x
|10x
|10x
|10x
|10x
|10x
|10x
|10x
|-
 
|-
|-style="background:LightGrey; color:black; vertical-align:middle; text-align:left;"
!Special features
|Stereoscopic microscope
|IR imaging
|
|
|
|
*Motorized stage
*'''[[Specific_Process_Knowledge/Characterization/Optical microscope/Nikon Eclipse L200 auto scan guide|Auto scan guide]]'''
|
|
|
|
|
|
|
|
|Stereoscopic microscope
|
|
|-
|-
|Bright field
 
|yes
|yes
|yes
|yes
|yes
|yes
|-
|-
| Dark field
|-style="background:WhiteSmoke; color:black; vertical-align:middle; text-align:left;"
|yes
!Contrast mechanisms
|yes
|
|yes
*Brightfield
|yes
|
|yes
*Polarizer
|yes
*Brightfield
|
*Brightfield
*Darkfield
|
*Polarizer
*Brightfield
|
*Brightfield
*Darkfield
|
*Brightfield
*Darkfield
|
*Polarizer
*Brightfield
*Darkfield
|
*Polarizer
*Brightfield
*Darkfield
|
*Polarizer
*Brightfield
*Darkfield
|
*Brightfield
|
*Brightfield
*Darkfield
|-
|-
|Polarizer
 
|yes
|no
|no
|yes
|yes
|no
|-
|-
|Episcopic light (reflected light)
|-style="background:LightGrey; color:black; vertical-align:middle; text-align:left;"
|yes
!Illumination modes
|yes
|
|yes
*Episcopic
|yes
|
|yes
*Episcopic
|yes
*Diascopic
|
*Episcopic
*Diascopic
|
*Episcopic
*Diascopic
|
*Episcopic
*Diascopic
|
*Episcopic
*Diascopic
|
*Episcopic
*Diascopic
|
*Episcopic
*Diascopic
|
*Episcopic
|
*Episcopic
|
*Episcopic
*Diascopic
|-
|-
|Diascopic light (transmitted light)
 
|no
|yes
|yes
|no
|no
|yes
|-
|-
|View with eye
|-style="background:WhiteSmoke; color:black; vertical-align:middle; text-align:left;"
|yes
!Camera
|yes
|None
|yes
|IR camera
|yes
|DS-Fi2
|yes
|None
|yes
|DS-Fi1
|DS-Fi1
|
*DS-Fi2
*C-mount, 0.7x relay
|
*DS-Fi2
*C-mount, 0.7x relay
|DS-Fi2
|None
|Infinity X
|-
|-
|View on screen
 
|no
|yes
|yes
|yes
|no
|yes
|-
|-
|Measurement option
|-style="background:LightGrey; color:black; vertical-align:middle; text-align:left;"
|no
!Analysis software
|no
|None
|yes
|None
|yes
|NIS-D
|no
|None
|yes
|NIS-BR
|NIS-D
|NIS-D
|NIS-D
|NIS-D
|None
|DeltaPix
|-
|-
|}
|}
<br clear="all" />
There are also two optical microscopes in building 451, a stereo microscope and a transmission microscope, that were both previously located in Packlab. Please ask staff / the BioMic group for details.

Latest revision as of 11:35, 7 November 2023

Feedback to this page: click here

This page is written by DTU Nanolab internal

Nikon SMZ 1000 Noco IR Leica INM 100 Zeiss Jenatech Nikon Eclipse L200 #1 Nikon Eclipse L200 #2 Nikon Eclipse L200N #3 Nikon Eclipse L200N #4 Nikon ME 600 Leica S8 APO Zeiss Axiotron
Location 346-901 346-901 346-901 cleanroom A1 cleanroom D3 cleanroom F3 cleanroom E4 cleanroom E5 cleanroom F1 cleanroom Cx1 cleanroom D3
Responsible group Wet chemistry Wet chemistry Wet chemistry Lithography Lithography Lithography Lithography Lithography Lithography Lithography Lithography
Objectives Zoom 0.8x - 8x
  • 2.5x
  • 10x
  • 20x
  • 50x
  • 2.5x
  • 5x
  • 10x
  • 20x
  • 50x
  • 5x
  • 10x
  • 20x
  • 50x
  • 100x
  • 2.5x
  • 5x
  • 10x
  • 20x
  • 50x
  • 2.5x
  • 5x
  • 10x
  • 20x
  • 50x
  • 100x
  • 2.5x
  • 5x
  • 10x
  • 20x
  • 50x
  • 100x
  • 2.5x
  • 5x
  • 10x
  • 20x
  • 50x
  • 100x
  • 5x
  • 10x
  • 20x
  • 50x
  • 100x
 Zoom 1x - 8x
  • 5x
  • 10x
  • 20x
  • 50x
Ocular 10x 10x 10x 10x 10x 10x 10x 10x 10x 10x 10x
Special features Stereoscopic microscope IR imaging Stereoscopic microscope
Contrast mechanisms
  • Brightfield
  • Polarizer
  • Brightfield
  • Brightfield
  • Darkfield
  • Polarizer
  • Brightfield
  • Brightfield
  • Darkfield
  • Brightfield
  • Darkfield
  • Polarizer
  • Brightfield
  • Darkfield
  • Polarizer
  • Brightfield
  • Darkfield
  • Polarizer
  • Brightfield
  • Darkfield
  • Brightfield
  • Brightfield
  • Darkfield
Illumination modes
  • Episcopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Diascopic
  • Episcopic
  • Episcopic
  • Episcopic
  • Diascopic
Camera None IR camera DS-Fi2 None DS-Fi1 DS-Fi1
  • DS-Fi2
  • C-mount, 0.7x relay
  • DS-Fi2
  • C-mount, 0.7x relay
 DS-Fi2 None Infinity X
Analysis software None None NIS-D None NIS-BR NIS-D NIS-D NIS-D NIS-D None DeltaPix


There are also two optical microscopes in building 451, a stereo microscope and a transmission microscope, that were both previously located in Packlab. Please ask staff / the BioMic group for details.

Retrieved from "https://labadviser.nanolab.dtu.dk//index.php?title=Specific_Process_Knowledge/Characterization/Optical_microscope&oldid=48209"