Passaging A1 cell: Difference between revisions

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<h4>For passaging 3 flasks of A1 cells:</h4>
== Material ==
<li>1 flask into 3 flasks and
* APBS (100 ml PBS + 25 ml ddwater)
<li>2 flasks into 2 x 10 cm plates (for making myotubes)
* TE in APBS (36 ml APBS + 4 ml TE)
* Gelatin (warmed to 37ºC)
* HS for A1 cells
* 1x 15 ml FALCON tubes
* Pipettes
* 3x 175 cm2 flasks


<h3>Materials :</h3>
== Procedure ==
<li>HS AMEM (see additional protocol for recipe)
# put 10 ml Gelatin into the new 175 cm2 flasks ( transfer the gelatine from the first to the second and from the second into the third → remove the remaining liquid)
<li>APBS ( 100 mls PBS + 25 mls water )
# aspirate the old media from the cells
<li>50 ml conical tube of 0.75% gelatin ( warmed to 37 degrees C )
# wash the cells 1 times with 5 ml APBS
<li>0.05% Trypsin/EDTA  ( 36 ml APBS + 4 ml 10x TE )
# remove the APBS
<li>1x unplugged pasteur pipettes
# add 5 ml TE
<li>20 ml pipettes
# wait till the cells are detached
<li>10 ml pipettes
# stop the TE with 5 ml HS – media
<li>3 large flasks-162 cm2
# centrifuge at 1000 rpm, 3 min at 4ºC
<li>2  10 cm plates
# aspirate the supernatant
<li>3 conical tubes, 15 ml
# dissolve the pellet into 3 ml fresh media
<li>1 scalpel no. 10
# fill in the new flasks 25 ml HS for A1 cells
# add into each flask 1 ml of the cell suspention


 
''The cells grow at 25ºC''
<h3>Execution:</h3>
 
Prepare plates and flasks
# score the 10 cm plates using the scalpel making 0.5 x 0.5 cm square grid across the plate.  (This limits the size of the myotubes to a reasonable size)
# --put 10 mls gelatin into each black cap flask and coat the bottom of the flask
--transfer the gelatin from the first flask into the second and coat, then the same procedure for the third flask
--then coat the 10 cm plates
Passage the cells
# aspirate  media off of the flask containing the cells
# Rinse  each black cap flask with 7 mls APBS
# aspirate off the APBS
# take 6 ml TE and put in flask
# wait until almost all cells come off
# stop with 3 mls HS AMEM in each flask
# mix with a pipette using the flow from pipette to detach any adherent cells
# put the cells into the 15 ml conical tube
# centrifuge ( spin 1000 rpm for 3 minutes )
# while you are waiting put 25 mls HS AMEM into each new flask and 10 mls into each 10 cm plate
# aspirate off the liquid in each conical tube
# flasks. use a pipette and resuspend cells in 6 mls HS MEM and put 2 mls of resuspension into each new flask! 10 cm plates: resuspend 2 flasks in 4 mls HS MEM and put 2 mls of resuspension into each 10 cm dish
# check cells  in the microscope
# label with cell type, passage number , date and name
put cells in 25 °c and 2 % CO2 incubator

Latest revision as of 14:23, 8 June 2015

Material

  • APBS (100 ml PBS + 25 ml ddwater)
  • TE in APBS (36 ml APBS + 4 ml TE)
  • Gelatin (warmed to 37ºC)
  • HS for A1 cells
  • 1x 15 ml FALCON tubes
  • Pipettes
  • 3x 175 cm2 flasks

Procedure

  1. put 10 ml Gelatin into the new 175 cm2 flasks ( transfer the gelatine from the first to the second and from the second into the third → remove the remaining liquid)
  2. aspirate the old media from the cells
  3. wash the cells 1 times with 5 ml APBS
  4. remove the APBS
  5. add 5 ml TE
  6. wait till the cells are detached
  7. stop the TE with 5 ml HS – media
  8. centrifuge at 1000 rpm, 3 min at 4ºC
  9. aspirate the supernatant
  10. dissolve the pellet into 3 ml fresh media
  11. fill in the new flasks 25 ml HS for A1 cells
  12. add into each flask 1 ml of the cell suspention

The cells grow at 25ºC

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