Team:EPF-Lausanne/Protocol/TrypanBlue

From 2012.igem.org

(Difference between revisions)
Line 2: Line 2:
{{:Team:EPF-Lausanne/Template/ProtocolHeader| Trypan Blue Method | {{{1|}}}}}
{{:Team:EPF-Lausanne/Template/ProtocolHeader| Trypan Blue Method | {{{1|}}}}}
-
{|
+
{
-
| align="center" style="background:#f0f0f0;"|''''''
+
<table>
-
| align="center" style="background:#f0f0f0;"|'''Sampling'''
+
<tr>
-
| align="center" style="background:#f0f0f0;"|''''''
+
<td> Cell density (10^6 ml) </td>
-
| align="center" style="background:#f0f0f0;"|''''''
+
<td> Dilution</td>
-
| align="center" style="background:#f0f0f0;"|''''''
+
<td> PBS (µl)</td>
-
| align="center" style="background:#f0f0f0;"|''''''
+
<td> Cells (µl) </td>
-
|-
+
<td>Trypan Blue (µl) </td>
-
| Dilutions||Cell Density ( 10^6/ml)||Dilution||PBS (µL)||Cells (µL)||Trypan Blue(µL)
+
</tr>
-
|-
+
<tr>
-
| ||1-2||4||100||50||50
+
<td> 1-2 </td>
-
|-
+
<td> 4 </td>
-
| ||2- 4.5||8||125||25||50
+
<td> 100 </td>
-
|-
+
<td> 50 </td>
-
| ||4.5 - 7||12||120||15||45
+
<td> 50 </td>
-
|-
+
</tr>
-
| ||>7||16||137.5||12.5||50
+
<tr>
-
|}
+
<td> 2-4.5 </td>
-
 
+
<td> 8 </td>
 +
<td> 125 </td>
 +
<td> 50 </td>
 +
</tr>
 +
<tr>
 +
<td> 4.5-7 </td>
 +
<td> 12 </td>
 +
<td> 120 </td>
 +
<td> 15 </td>
 +
<td> 45 </td>
 +
</tr>
 +
<tr>
 +
<td> >7 </td>
 +
<td> 16 </td>
 +
<td> 137.5 </td>
 +
<td> 12.5 </td>
 +
<td> 50 </td>
 +
</tr>
 +
</table>
#Take xµL ofPBS in 96 well plate
#Take xµL ofPBS in 96 well plate

Revision as of 16:29, 16 September 2012

Protocol: Trypan Blue Method

{

Cell density (10^6 ml) Dilution PBS (µl) Cells (µl) Trypan Blue (µl)
1-2 4 100 50 50
2-4.5 8 125 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