Bitan:MicrogliaIHC: Difference between revisions

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Bring section under focus in StereoInvestigator
== Bring section under focus in StereoInvestigator ==
 


Acquisition → Acquire Image
Acquisition → Acquire Image


Click on the image, but not on the section
*Click on the image, but not on the section


Image → Add Scalebar
Image → Add Scalebar


Set to 100 microns
*Set to 100 microns


Apply Scalebar
*Apply Scalebar


To get to the next section revert back to Live Image and Select New Data File
To get to the next section revert back to Live Image and Select New Data File


Open Image in ImageJ
 
== Open Image in ImageJ ==


Open a second image
Open a second image


Both Images:
Both Images:
Image → Type → 8-bit
 
*Image → Type → 8-bit


One Image:
One Image:
Analyze → Set Scale
 
70 pixels → 100 μm
*Analyze → Set Scale
Process → Subtract Background
 
50 pixels rolling ball radius
:* 70 pixels → 100 μm
Check Light Background
 
Use color picker to pick a color closest to white
*Process → Subtract Background
Use pencil to whiteout all dark areas not part of the spinal section or are “spots” on the section
 
Image → Adjust → Brightness and Contrast
:*50 pixels rolling ball radius
Adjust min/max bars until microglia are clearly contrasting the background
 
Compare with other 8 bit image
:*Check Light Background
Image → Adjust → Threshould
 
Adjust Threshold value until microglia are selected and as much background is removed as possible
*Use color picker to pick a color closest to white
Use zoom tool to compare with 8-bit image
 
Analyze→ Analyze Particles
*Use pencil to whiteout all dark areas not part of the spinal section or are “spots” on the section
Select Summarize and DIsplay Measurement
 
Mark down: Count, Total Area, and Average Size
*Image → Adjust → Brightness and Contrast
 
:*Adjust min/max bars until microglia are clearly contrasting the background
 
:*Compare with other 8 bit image
 
*Image → Adjust → Threshold
 
:*Adjust Threshold value until microglia are selected and as much background is removed as possible
 
:*Use zoom tool to compare with 8-bit image
 
*Analyze→ Analyze Particles
 
:*Select Summarize and DIsplay Measurement
 
:*Mark down: Count, Total Area, and Average Size

Latest revision as of 04:33, 5 September 2015

Bring section under focus in StereoInvestigator

Acquisition → Acquire Image

  • Click on the image, but not on the section

Image → Add Scalebar

  • Set to 100 microns
  • Apply Scalebar

To get to the next section revert back to Live Image and Select New Data File


Open Image in ImageJ

Open a second image

Both Images:

  • Image → Type → 8-bit

One Image:

  • Analyze → Set Scale
  • 70 pixels → 100 μm
  • Process → Subtract Background
  • 50 pixels rolling ball radius
  • Check Light Background
  • Use color picker to pick a color closest to white
  • Use pencil to whiteout all dark areas not part of the spinal section or are “spots” on the section
  • Image → Adjust → Brightness and Contrast
  • Adjust min/max bars until microglia are clearly contrasting the background
  • Compare with other 8 bit image
  • Image → Adjust → Threshold
  • Adjust Threshold value until microglia are selected and as much background is removed as possible
  • Use zoom tool to compare with 8-bit image
  • Analyze→ Analyze Particles
  • Select Summarize and DIsplay Measurement
  • Mark down: Count, Total Area, and Average Size