Team:EPF-Lausanne/Protocol/TrypanBlue

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{{:Team:EPF-Lausanne/Template/ProtocolHeader| Trypan Blue Method | {{{1|}}}}}
{{:Team:EPF-Lausanne/Template/ProtocolHeader| Trypan Blue Method | {{{1|}}}}}
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<table>
 
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<caption> Sampling </caption>
 
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<tr>
 
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<td> Cell density (10^6 ml) </td>
 
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<td> Dilution</td>
 
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<td> PBS (µl)</td>
 
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<td> Cells (µl) </td>
 
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<td>Trypan Blue (µl) </td>
 
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</tr>
 
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<tr>
 
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<td> 1-2 </td>
 
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<td> 4 </td>
 
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<td> 100 </td>
 
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<td> 50 </td>
 
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<td> 50 </td>
 
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</tr>
 
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<tr>
 
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<td> 2-4.5 </td>
 
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<td> 8 </td>
 
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<td> 125 </td>
 
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<td> 50 </td>
 
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</tr>
 
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<tr>
 
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<td> 4.5-7 </td>
 
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<td> 12 </td>
 
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<td> 120 </td>
 
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<td> 15 </td>
 
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<td> 45 </td>
 
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</tr>
 
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<tr>
 
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<td> >7 </td>
 
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<td> 16 </td>
 
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<td> 137.5 </td>
 
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<td> 12.5 </td>
 
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<td> 50 </td>
 
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</tr>
 
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</table>
 
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=== Sampling ===
=== Sampling ===
{| class="wikitable" style="text-align: center; color: black;"
{| class="wikitable" style="text-align: center; color: black;"
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|Cell Density
+
|Cell Density ( 10^6 ml)
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|Dilution
+
|Dilution      
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|PBS
+
|PBS             ( µl )
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|Cells
+
|Cells           ( µl )
-
|Trypan Blue
+
|Trypan Blue ( µl)
|-
|-
|1-2
|1-2

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