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

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{| border="1" cellspacing="0" cellpadding="6"  
{{cc-nanolab}}
!  
 
! Zeiss (RR2)
'''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]'''
! 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<br>D-3?
|cleanroom<br>D-3
|cleanroom<br>A-1
|cleanroom<br>D-3
|cleanroom<br>E-5
|cleanroom<br>F-1?
|cleanroom<br>Cx1
|cleanroom<br>F-3
|-
 
|-
|-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.
Retrieved from "https://labadviser.nanolab.dtu.dk//index.php?title=Specific_Process_Knowledge/Characterization/Optical_microscope"