Team:EPF-Lausanne/Notebook/19 July 2012

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(→Afternoon: Cell lysates)
(→Morning: Cell counting and sampling)
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Given our cell density we used a 12x dilution (table). We transfered 6 samples of cells into a 96 well plate, added Trypan blue and analysed each sample with Countess.  
Given our cell density we used a 12x dilution (table). We transfered 6 samples of cells into a 96 well plate, added Trypan blue and analysed each sample with Countess.  
-
[table with results]
+
{| class="wikitable" style="text-align: center; color: black;"
 +
|'''Sample #'''
 +
|'''Viable cells'''
 +
|'''Dead cells'''
 +
|'''Viability'''
 +
|'''Total cells'''
 +
|-
 +
|1
 +
|182
 +
|12
 +
|94%
 +
|194
 +
|-
 +
|3
 +
|112
 +
|7
 +
|94%
 +
|119
 +
|-
 +
|5
 +
|124
 +
|8
 +
|94%
 +
|132
 +
|-
 +
|7
 +
|129
 +
|16
 +
|89%
 +
|145
 +
|-
 +
|9
 +
|170
 +
|3
 +
|98%
 +
|173
 +
|-
 +
|11
 +
|127
 +
|9
 +
|93%
 +
|136
 +
|-
 +
|}
 +
*Average cell # for samples 3.5.7 = 122 cells
 +
*LCD: 122*12/400 = 3.66 mio cells/ml
 +
-> we need to take 1.37ml to obtain 5 mio cells.
 +
 
 +
; Comments:
 +
Sample 7 has been excluded because of bubble-like structures which appeared while scanning and were confused with cells clusters by the program.
; '''Western Blot sampling'''
; '''Western Blot sampling'''

Revision as of 23:33, 19 July 2012

Contents

Morning: Cell counting and sampling

Cell counting

Given our cell density we used a 12x dilution (table). We transfered 6 samples of cells into a 96 well plate, added Trypan blue and analysed each sample with Countess.

Sample # Viable cells Dead cells Viability Total cells
1 182 12 94% 194
3 112 7 94% 119
5 124 8 94% 132
7 129 16 89% 145
9 170 3 98% 173
11 127 9 93% 136
  • Average cell # for samples 3.5.7 = 122 cells
  • LCD: 122*12/400 = 3.66 mio cells/ml

-> we need to take 1.37ml to obtain 5 mio cells.

Comments

Sample 7 has been excluded because of bubble-like structures which appeared while scanning and were confused with cells clusters by the program.

Western Blot sampling

Protocol (add to separate page):

  1. Centrifugation of the cell samples at 2500xg for 10min. Discard the supernatant (vacuum).
  2. Washing: Resuspend the pellet in PBS1x, centrifuge at 2500xg for 10min, discard supernatant.
  3. Add at least 1mL PER-M Reagent for 100mg (~100µl) of cell pellet. Pipette up and down to suspend.
  4. Shake gently for 10min.
  5. Remove cell bedris by centrifugation: ~1400xg for 15min
  6. Transfer the supernatant into new tubes for analysis or storage.
  • Samples where taken from odd numbered tubes : 1,3,5,7.
  • We used 300µl of M-PER Reagent based on the size of our pellets.
  • Maximum centrifugation was 10'600xg.


Protocol: None

Forgot to insert protocol.


Comments

For samples 3 and 5 we had to repeat step 5 (centrifugation to remove cell debris) because the cell pellet got aspired in the pipette while trying to transfer the supernantant into fresh tubes.

Afternoon: Cell lysates

We prepared cell lysates for future mRNA sampling and for analysing fluorescence the same day.

Protocol: Sampling for Tecan machine (add on separate page)
  1. Take ~1mio cells in 750 µl PBS
  2. Centriguge samples at 450xg for 5min
  3. Remove the supernatant (vaccum)
  4. Resuspend in 200µl of 1% TritonX in PBS
  5. Load onto black well and leave on the shaker for 1 hour.
  6. Read fluorescence on Tecan machine

Protocol: Sampling for mRNA (add on separate page)

  1. Take ~1mio cells in 750 µl PBS
  2. Centriguge samples at 450xg for 5min
  3. Remove the supernatant (vaccum) leaving 50µl.
  4. Vortex and resuspend.
  5. Add 1µl PBS, vortex again.
  6. Centrifuge at 450xg for 5min
  7. Remove supernatant (pipette) and freeze in liquid nitrogen. Store at -20°C.


Protocol: None

Forgot to insert protocol.


Comments

Our cell density was 6mio cells/ml, therefore we needed to take a volume of 170µl to have 1mio cells/ml.

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