Measuring Phagocytosis using pHrodo Bioparticles
From Bridges Lab Protocols
Materials
- pHrodo BioParticles Conjugates (Invitrogen cat #A10010)
- HBSS
- OptiMEM
Protocol
- Subculture cells 3-4 days in advance
- On the day of the assay, harvest cells and spin down. Resuspend in OptiMEM at 1 000 000 cells/mL
- Plate into a 96 well plate at 100 000 cells per well (100uL of a 1 000 000 cells/mL suspension), plating each condition in triplicate. Leave at least set of wells empty as a blank.
- Add 100 uL of OptiMEM to blank wells.
- Incubate at least 1h at 37C in a CO2 incubator.
- Treat wells as desired.
- Thaw one vial of particles for every 20 wells (including no cell controls). Add 2 mL HBSS to a vial and vortex briefly.
- Transfer to a clean glass tube and sonicate for 5 min to ensure even dispersion.
- After cells have adhered, aspirate media.
- Replace media with 100 uL of the resuspended bioparticles.
- Put in incubator for 2-3h
- Scan plate using 550nm excitation and 600nm emission