Difference between revisions of "Seahorse - Mitochondrial Stress Test"

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[[ Category: Seahorse ]]
 
[[ Category: Seahorse ]]
 
[[ Category: Mitochondrial Function ]]
 
[[ Category: Mitochondrial Function ]]
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 +
==Materials==
 +
* [[Seahorse XF Media]]
 +
* XF Cartridge
 +
* Cells in XF24 plate, either grown in the plate or seeded at a previously established density where the OCR is 40-500 mL/min.
 +
* Injection stock solutions (1 mM Oligomycin, 1 mM FCCP, 1 mM Rotenone and 1 mM Antimycin A) made up in DMSO at 1000X.  Aliquots in the -20 in '''Seahorse Reagents''' box.
 +
* Check if the machine is free.
 +
 +
==Protocol==
 +
 +
===The Day Before the Assay===
 +
* Hydrate a cartridge by placing 1 mL/well of XF Calibration Media into each well of a XF24 cartridge.  Place in non-CO2, humidified, 37C incubator overnight to hydrate.
 +
* Ensure that there is sufficient XF media and stock solutions.
 +
* Prepare cells if necessary, leave in CO2 incubator overnight.  Make sure to leave blank wells (typically A5, B3, C4, D2).
 +
 +
===The Day of the Assay===
 +
* Prepare media by the following steps:
 +
** Place 100mL in non-CO2, humidified, 37C incubator for ~30 minutes to warm up.
 +
** Add the following solutions (these are standard concentrations and may be slightly different for your cell line of interest):
 +
*** 10 mM Glucose (1 mL of a 1M stock into 100 mL)
 +
*** 2 mM Glutamine (1 mL of a 200 mM stock)
 +
*** 1 mM Pyruvate (100 uL of a 1M stock)
 +
** Re-adjust the pH to 7.4 (7.35-7.45)
 +
* Wash cells twice with 500 mL of pre-warmed media, add 500 uL final volume to each well
 +
* Incubate for 1h in non-CO2, humidified, 37C incubator to get rid of any extra CO2
 +
* While plate is incubating, prepare injection solutions in 1.8 mL of prepared XF Media.  These are standard concentrations, and should be optimized for your system (especially FCCP)
 +
** '''Tube A''' 18 uL Oligomycin
 +
** '''Tube B''' 18 uL FCCP
 +
** '''Tube C''' 9 uL Rotenone and 9 uL Antimycin A
 +
* Add the compounds to the injection ports in the cartridge (A, bottom right; B bottom left; C top right).  '''Make sure the barcode is on the right hand side.'''
 +
* Set up your protocol, editing a similar template and saving with the date and experiment type
 +
* Start the protocol, inserting the cartridge.  '''Make sure the barcode is on the right hand side.'''
 +
* Once the cartridge is calibrated insert the cell plate at the prompt.  If the calibration fails, abort the run and try the calibration again

Revision as of 20:06, 22 May 2017


Materials

  • Seahorse XF Media
  • XF Cartridge
  • Cells in XF24 plate, either grown in the plate or seeded at a previously established density where the OCR is 40-500 mL/min.
  • Injection stock solutions (1 mM Oligomycin, 1 mM FCCP, 1 mM Rotenone and 1 mM Antimycin A) made up in DMSO at 1000X. Aliquots in the -20 in Seahorse Reagents box.
  • Check if the machine is free.

Protocol

The Day Before the Assay

  • Hydrate a cartridge by placing 1 mL/well of XF Calibration Media into each well of a XF24 cartridge. Place in non-CO2, humidified, 37C incubator overnight to hydrate.
  • Ensure that there is sufficient XF media and stock solutions.
  • Prepare cells if necessary, leave in CO2 incubator overnight. Make sure to leave blank wells (typically A5, B3, C4, D2).

The Day of the Assay

  • Prepare media by the following steps:
    • Place 100mL in non-CO2, humidified, 37C incubator for ~30 minutes to warm up.
    • Add the following solutions (these are standard concentrations and may be slightly different for your cell line of interest):
      • 10 mM Glucose (1 mL of a 1M stock into 100 mL)
      • 2 mM Glutamine (1 mL of a 200 mM stock)
      • 1 mM Pyruvate (100 uL of a 1M stock)
    • Re-adjust the pH to 7.4 (7.35-7.45)
  • Wash cells twice with 500 mL of pre-warmed media, add 500 uL final volume to each well
  • Incubate for 1h in non-CO2, humidified, 37C incubator to get rid of any extra CO2
  • While plate is incubating, prepare injection solutions in 1.8 mL of prepared XF Media. These are standard concentrations, and should be optimized for your system (especially FCCP)
    • Tube A 18 uL Oligomycin
    • Tube B 18 uL FCCP
    • Tube C 9 uL Rotenone and 9 uL Antimycin A
  • Add the compounds to the injection ports in the cartridge (A, bottom right; B bottom left; C top right). Make sure the barcode is on the right hand side.
  • Set up your protocol, editing a similar template and saving with the date and experiment type
  • Start the protocol, inserting the cartridge. Make sure the barcode is on the right hand side.
  • Once the cartridge is calibrated insert the cell plate at the prompt. If the calibration fails, abort the run and try the calibration again