Difference between revisions of "Seahorse - Mitochondrial Stress Test"
From Bridges Lab Protocols
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* 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.''' | * 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 | * 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.''' | + | * Start the protocol, inserting the cartridge with the lid removed. '''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 | * 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 17:02, 14 June 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 uL 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 with the lid removed. 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
