Team:EPF-Lausanne/Protocol/TrypanBlue

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(Difference between revisions)
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#Add required volume of cell culture. Mix once
#Add required volume of cell culture. Mix once
#Bring the plate back to microscope, add trypan blue to the PBS + Cell mixture just before counting the sample.  
#Bring the plate back to microscope, add trypan blue to the PBS + Cell mixture just before counting the sample.  
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  ==Trypan Blue is toxic to cells. If left too long with trypan blue, even healthy cells will die. ==
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  === Trypan Blue is toxic to cells. If left too long with trypan blue, even healthy cells will die. ===

Revision as of 16:42, 16 September 2012

Protocol: Trypan Blue Method

Sampling

Cell Density ( 10^6 ml) Dilution PBS ( µl ) Cells ( µl ) Trypan Blue ( µl)
1-2 4 100 50 50
2-4.5 8 125 25 50
4.5-7 12 120 15 45
>7 16 137.5 12.5 50


  1. Take xµL ofPBS in 96 well plate
  2. Add required volume of cell culture. Mix once
  3. Bring the plate back to microscope, add trypan blue to the PBS + Cell mixture just before counting the sample.
=== Trypan Blue is toxic to cells. If left too long with trypan blue, even healthy cells will die. ===


Calculation of LCD :

LCD = Cell Count/ ( 100* 4) * Dilution

Tips :

  1. Mix cells before sampling
  2. Take cell sample from top of the liquid
  3. Mix trepan blue into the PBS + cel solution slowly and well before loading