DAF-FM DA (solution)

Guide (The following is our recommended protocol. This protocol is only a guide and should be modified according to your specific needs).
1. Preparation of stock solution^[2]
It is recommended that the DAF-FM DA stock solution be stored at -20°C or -80°C in the dark after aliquoting.
2. Preparation of working solution
Dilute the stock solution with Hank’s buffer or serum-free medium. The corresponding stock solution can be diluted according to the actual situation. Note that if the solvent is DMSO, the cytotoxicity of DMSO must be considered, and a solvent control should be prepared; if the solvent is pure water, the working solution needs to be filtered and sterilized before adding cells.
Note: Please adjust the concentration of DAF-FM DA working solution according to actual conditions and prepare it before use.
3. Staining steps
3.1 Seed cells in a 6-well plate.
3.2 Aspirate the culture medium.
3.3 Add 5 μM DAF-FM DA working solution to each well and incubate at 37°C in the dark for 30 min to allow the probe to enter the cells.
3.4 Replace with fresh Hank’s buffer and continue incubation for 20 min to complete the deesterification reaction.
3.5 Counterstain the cell nucleus with Hoechst dye.
3.6 Quantify the fluorescence intensity using a microplate reader at 495 nm excitation and 515 nm emission, and normalize to the number of cells stained with Hoechst.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.